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Scientific Affairs Manager - Italy (Rome)

Rhythmpharmaceuticals · Rome · Active · JazzHR / ApplyToJob

Job facts

FieldValue
CompanyRhythmpharmaceuticals
TitleScientific Affairs Manager - Italy (Rome)
Normalized title-
Department / team-
LocationRome
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerJazzHR / ApplyToJob
Posted / first seen2026-06-19 / 2026-06-20
Changed / last seen2026-06-20 / 2026-06-22

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Linked records

CompanyRhythmpharmaceuticals
Sourcea089d8d0-2598-437f-b618-c2dc9cbdd98b
ATS providerJazzHR / ApplyToJob

Description

Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to learn, adapt, and our tenacity to overcome barriers, together . Opportunity Overview As a member of the Rhythm Italy field-based Medical Affairs team, the Scientific Affairs Manager (SAM) will focus on advancing medical and scientific initiatives in rare MC4R pathway diseases.  In close collaboration with the national and international Medical Affairs teams, the SAM will provide scientific and medical leadership and support for the implementation of integrated tactical and engagement plans, while upholding the highest standards of compliance and scientific integrity in Italy. You will be responsible for building peer-to-peer relationships with Key External Experts (KEEs) and other stakeholders to deliver clinical, scientific, and medical education.  Further, you will support research initiatives, advisory boards, and other compliant scientific exchange activities to support the integrated strategic and tactical plan and the Medical Affairs’ tactics. Responsibilities and Duties Serve as a Scientific Affairs Manager for Italy and as a member of the international Medical Affairs Team Be a subject-matter expert for the MC4R pathway diseases and our indications Contribute to the development and implementation of the integrated strategic and tactical plan with a focus on the medical and scientific projects and tactics. Organize and lead local advisory boards and KEE meetings to gain insights, foster scientific exchange and support the local strategy. Provide medical support for the implementation of the local strategy. Build and maintain peer-to-peer relationships with external experts and stakeholders, delivering clinical, scientific, and medical education. Oversee and initiate medical projects in collaboration with clinical partners and research networks. Identify stakeholders and provide insights for future clinical developments and play a key role in the pre-launch and launch phase for these new developments. Contribute to the development and implementation of scientific communication plans and medical information materials, ensuring compliance with local regulatory requirements. Identify knowledge gaps among healthcare professionals and organize non-promotional scientific presentations. Participate in local medical and cross-functional projects and initiatives. Ensure effective and compliant communication with internal and external stakeholders. Establish genetic testing initiatives in collaboration with HCPs and obesity treatment networks Support the commercial team and HCPs with knowledge building around the efficacy and safety of our product including AE/PV reporting. Play a pivotal role in establishing appropriate multidisciplinary care including patient support programs Play a pivotal role in identifying hurdles and solutions in order to optimize patient identification and referral pathways. Communicate key medical insights from KEEs and others to inform medical strategy Collaborate effectively across internal stakeholders (including Medical Affairs, Commercial and others) to ensure aligned execution, consistent communication, and compliance with company, legal, and regulatory requirements; contribute to Customer Relationship Management (CRM) documentation as appropriate. Respond to unsolicited requests for medical information in a timely manner. Ensure that an accurate and fair-balanced response is provided Qualifications and Skills Advanced degree in a pharmaceutical, scientific, or medical field (PharmD, PhD, MD) 8 or more years’ experience within a Medical Science Liaison or similar field facing role with primary emphasis on field based scientific exchange within the biopharmaceutical industry.  Relevant pharmaceutical and clinical/therapeutic experience also a consideration Rare diseases experience is a plus Launch experience is a plus Cross-functional mindset focused on a seamless collaboration with the commercial team Excellent communication and presentation skills - fluent in local language for the market and in verbal and written English Demonstrated knowledge of regional/local specific healthcare systems, the evolving medical landscape, reimbursement and industry trends.  Ability to work in collaboration with the international region and with a positive attitude. This role is field- based in Italy.  Candidates applying must be willing and able to work primarily out of their home office. This role will involve up to 50% travel. The expected salary range for this position is € 70 000 – € 105 000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units. More About Rhythm We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare melanocortin-4 receptor (MC4R) pathway diseases by rapidly advancing care and precision medicines that address the root cause.  Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism. At Rhythm Our Core Values Are •     We are committed to advancing scientific understanding to improve patients’ lives •     We are inspired to tackle tough challenges and have the courage to ask bold questions •     We are eager to learn and adapt •     We believe collaboration and ownership are foundational for our success •      We value the unique contribution each individual brings to furthering our mission

Full job record

Job ID6abbb713bd50e61af2fa214de75e333788768330
Org ID73fb8494-6154-4f75-bcac-7c8caae53a03
Source IDa089d8d0-2598-437f-b618-c2dc9cbdd98b
Board IDa089d8d0-2598-437f-b618-c2dc9cbdd98b
Providerjazzhr
Provider Job KeyOv7azLXlBS
TitleScientific Affairs Manager - Italy (Rome)
Normalized Title
Statusactive
Activeyes
Location TextRome
Department
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryRome
Region
City
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://rhythmpharmaceuticals.applytojob.com/apply/Ov7azLXlBS/Scientific-Affairs-Manager-Italy-Rome
Apply URLhttps://rhythmpharmaceuticals.applytojob.com/apply/Ov7azLXlBS/Scientific-Affairs-Manager-Italy-Rome
First Seen At2026-06-20 11:38:15Z
Last Seen At2026-06-22 14:38:50Z
Last Checked At2026-06-22 14:38:50Z
Last Changed At2026-06-20 11:38:15Z
Inactive At
Source Posted At2026-06-19 00:00:00Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=jazzhr/board=rhythmpharmaceuticals/date=2026-06-22/2026-06-22T14-38-45-577Z-287e0f6cc5156dc9378c73375f1fd1e374207b80d392c873c48f8d58887ba6a9.json
Event Fields
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Extensions
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Native Structured
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    "description_html": "<span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><strong>Company Overview</strong><br>Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to learn, adapt, and our tenacity to overcome barriers, together<b>.</b></span></span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><b><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\">Opportunity Overview</span></b></span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">As a member of the Rhythm Italy field-based Medical Affairs team, the Scientific Affairs Manager (SAM) will focus on advancing medical and scientific initiatives in rare MC4R pathway diseases.  In close collaboration with the national and international Medical Affairs teams, the SAM will provide scientific and medical leadership and support for the implementation of integrated tactical and engagement plans, while upholding the highest standards of compliance and scientific integrity in Italy.</span></span></span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">You will be responsible for building peer-to-peer relationships with Key External Experts (KEEs) and other stakeholders to deliver clinical, scientific, and medical education.  Further, you will support research initiatives, advisory boards, and other compliant scientific exchange activities to support the integrated strategic and tactical plan and the Medical Affairs’ tactics.</span></span></span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Responsibilities and Duties</span></span></b></span></span></span></span><ul><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Serve as a Scientific Affairs Manager for Italy and as a member of the international Medical Affairs Team</span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Be a subject-matter expert for the MC4R pathway diseases and our indications</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Contribute to the development and implementation of the integrated strategic and tactical plan with a focus on the medical and scientific projects and tactics.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Organize and lead local advisory boards and KEE meetings to gain insights, foster scientific exchange and support the local strategy.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Provide medical support for the implementation of the local strategy.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Build and maintain peer-to-peer relationships with external experts and stakeholders, delivering clinical, scientific, and medical education.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Oversee and initiate medical projects in collaboration with clinical partners and research networks.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Identify stakeholders and provide insights for future clinical developments and play a key role in the pre-launch and launch phase for these new developments. </span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Contribute to the development and implementation of scientific communication plans and medical information materials, ensuring compliance with local regulatory requirements.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Identify knowledge gaps among healthcare professionals and organize non-promotional scientific presentations.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Participate in local medical and cross-functional projects and initiatives.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Ensure effective and compliant communication with internal and external stakeholders.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Establish genetic testing initiatives in collaboration with HCPs and obesity treatment networks </span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\">Support the commercial team and HCPs with knowledge building around the efficacy and safety of our product including AE/PV reporting.</span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Play a pivotal role in establishing appropriate multidisciplinary care including patient support programs</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Play a pivotal role in identifying hurdles and solutions in order to optimize patient identification and referral pathways.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Communicate key medical insights from KEEs and others to inform medical strategy</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Collaborate effectively across internal stakeholders (including Medical Affairs, Commercial and others) to ensure aligned execution, consistent communication, and compliance with company, legal, and regulatory requirements; contribute to Customer Relationship Management (CRM) documentation as appropriate.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Respond to unsolicited requests for medical information in a timely manner. Ensure that an accurate and fair-balanced response is provided</span></span></span></span></span></span></span></li></ul><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Qualifications and Skills</span></span></b></span></span></span></span><ul><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Advanced degree in a pharmaceutical, scientific, or medical field (PharmD, PhD, MD) </span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">8 or more years’ experience within a Medical Science Liaison or similar field facing role with primary emphasis on field based scientific exchange within the biopharmaceutical industry.  Relevant pharmaceutical and clinical/therapeutic experience also a consideration</span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Rare diseases experience is a plus</span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\">Launch experience is a plus</span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Cross-functional mindset focused on a seamless collaboration with the commercial team</span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Excellent communication and presentation skills - fluent in local language for the market and in verbal and written English</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Demonstrated knowledge of regional/local specific healthcare systems, the evolving medical landscape, reimbursement and industry trends. </span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Ability to work in collaboration with the international region and with a positive attitude.</span></span></span></span></span></span></li></ul><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#4472c4;\">This role is field- based in Italy.  Candidates applying must be willing and able to work primarily out of their home office. This role will involve up to 50% travel.</span></span></span></i></span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#4472c4;\">The expected salary range for this position is € 70 000 – € 105 000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units. </span></span></span></i></span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"><strong>More About Rhythm</strong><br>We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare melanocortin-4 receptor (MC4R) pathway diseases by rapidly advancing care and precision medicines that address the root cause.  Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.</span></span></i></span></span></span></span><br><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">At Rhythm Our Core Values Are</span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•     We are committed to advancing scientific understanding to improve patients’ lives</span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•     We are inspired to tackle tough challenges and have the courage to ask bold questions</span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•     We are eager to learn and adapt</span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•     We believe collaboration and ownership are foundational for our success<br>•     </span></span></span></span></i></span></span></span><i style=\"font-family:Aptos, sans-serif;font-size:12pt;\"><span lang=\"en-us\" style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">We value the unique contribution each individual brings to furthering our mission</span></span></span></span></i><br><br> ",
    "description_text": "Company Overview\nRhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to learn, adapt, and our tenacity to overcome barriers, together .\n Opportunity Overview\n As a member of the Rhythm Italy field-based Medical Affairs team, the Scientific Affairs Manager (SAM) will focus on advancing medical and scientific initiatives in rare MC4R pathway diseases.  In close collaboration with the national and international Medical Affairs teams, the SAM will provide scientific and medical leadership and support for the implementation of integrated tactical and engagement plans, while upholding the highest standards of compliance and scientific integrity in Italy.\n You will be responsible for building peer-to-peer relationships with Key External Experts (KEEs) and other stakeholders to deliver clinical, scientific, and medical education.  Further, you will support research initiatives, advisory boards, and other compliant scientific exchange activities to support the integrated strategic and tactical plan and the Medical Affairs’ tactics.\n Responsibilities and Duties Serve as a Scientific Affairs Manager for Italy and as a member of the international Medical Affairs Team\n Be a subject-matter expert for the MC4R pathway diseases and our indications\n Contribute to the development and implementation of the integrated strategic and tactical plan with a focus on the medical and scientific projects and tactics.\n Organize and lead local advisory boards and KEE meetings to gain insights, foster scientific exchange and support the local strategy.\n Provide medical support for the implementation of the local strategy.\n Build and maintain peer-to-peer relationships with external experts and stakeholders, delivering clinical, scientific, and medical education.\n Oversee and initiate medical projects in collaboration with clinical partners and research networks.\n Identify stakeholders and provide insights for future clinical developments and play a key role in the pre-launch and launch phase for these new developments.\n Contribute to the development and implementation of scientific communication plans and medical information materials, ensuring compliance with local regulatory requirements.\n Identify knowledge gaps among healthcare professionals and organize non-promotional scientific presentations.\n Participate in local medical and cross-functional projects and initiatives.\n Ensure effective and compliant communication with internal and external stakeholders.\n Establish genetic testing initiatives in collaboration with HCPs and obesity treatment networks\n Support the commercial team and HCPs with knowledge building around the efficacy and safety of our product including AE/PV reporting.\n Play a pivotal role in establishing appropriate multidisciplinary care including patient support programs\n Play a pivotal role in identifying hurdles and solutions in order to optimize patient identification and referral pathways.\n Communicate key medical insights from KEEs and others to inform medical strategy\n Collaborate effectively across internal stakeholders (including Medical Affairs, Commercial and others) to ensure aligned execution, consistent communication, and compliance with company, legal, and regulatory requirements; contribute to Customer Relationship Management (CRM) documentation as appropriate.\n Respond to unsolicited requests for medical information in a timely manner. Ensure that an accurate and fair-balanced response is provided\n Qualifications and Skills Advanced degree in a pharmaceutical, scientific, or medical field (PharmD, PhD, MD)\n 8 or more years’ experience within a Medical Science Liaison or similar field facing role with primary emphasis on field based scientific exchange within the biopharmaceutical industry.  Relevant pharmaceutical and clinical/therapeutic experience also a consideration\n Rare diseases experience is a plus\n Launch experience is a plus\n Cross-functional mindset focused on a seamless collaboration with the commercial team\n Excellent communication and presentation skills - fluent in local language for the market and in verbal and written English\n Demonstrated knowledge of regional/local specific healthcare systems, the evolving medical landscape, reimbursement and industry trends.\n Ability to work in collaboration with the international region and with a positive attitude.\n This role is field- based in Italy.  Candidates applying must be willing and able to work primarily out of their home office. This role will involve up to 50% travel.\n The expected salary range for this position is € 70 000 – € 105 000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units.\n More About Rhythm\nWe are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare melanocortin-4 receptor (MC4R) pathway diseases by rapidly advancing care and precision medicines that address the root cause.  Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.\n At Rhythm Our Core Values Are\n •     We are committed to advancing scientific understanding to improve patients’ lives\n •     We are inspired to tackle tough challenges and have the courage to ask bold questions\n •     We are eager to learn and adapt\n •     We believe collaboration and ownership are foundational for our success\n•      We value the unique contribution each individual brings to furthering our mission",
    "jsonld_jobposting": {
      "url": "https://rhythmpharmaceuticals.applytojob.com/apply/Ov7azLXlBS/Scientific-Affairs-Manager-Italy-Rome",
      "@type": "JobPosting",
      "title": "Scientific Affairs Manager - Italy (Rome)",
      "@context": "http://schema.org/",
      "datePosted": "2026-06-19",
      "description": "<span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><strong>Company Overview</strong><br>Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to learn, adapt, and our tenacity to overcome barriers, together<b>.</b></span></span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><b><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\">Opportunity Overview</span></b></span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">As a member of the Rhythm Italy field-based Medical Affairs team, the Scientific Affairs Manager (SAM) will focus on advancing medical and scientific initiatives in rare MC4R pathway diseases.  In close collaboration with the national and international Medical Affairs teams, the SAM will provide scientific and medical leadership and support for the implementation of integrated tactical and engagement plans, while upholding the highest standards of compliance and scientific integrity in Italy.</span></span></span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">You will be responsible for building peer-to-peer relationships with Key External Experts (KEEs) and other stakeholders to deliver clinical, scientific, and medical education.  Further, you will support research initiatives, advisory boards, and other compliant scientific exchange activities to support the integrated strategic and tactical plan and the Medical Affairs’ tactics.</span></span></span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Responsibilities and Duties</span></span></b></span></span></span></span><ul><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Serve as a Scientific Affairs Manager for Italy and as a member of the international Medical Affairs Team</span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Be a subject-matter expert for the MC4R pathway diseases and our indications</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Contribute to the development and implementation of the integrated strategic and tactical plan with a focus on the medical and scientific projects and tactics.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Organize and lead local advisory boards and KEE meetings to gain insights, foster scientific exchange and support the local strategy.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Provide medical support for the implementation of the local strategy.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Build and maintain peer-to-peer relationships with external experts and stakeholders, delivering clinical, scientific, and medical education.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Oversee and initiate medical projects in collaboration with clinical partners and research networks.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Identify stakeholders and provide insights for future clinical developments and play a key role in the pre-launch and launch phase for these new developments. </span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Contribute to the development and implementation of scientific communication plans and medical information materials, ensuring compliance with local regulatory requirements.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Identify knowledge gaps among healthcare professionals and organize non-promotional scientific presentations.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Participate in local medical and cross-functional projects and initiatives.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Ensure effective and compliant communication with internal and external stakeholders.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Establish genetic testing initiatives in collaboration with HCPs and obesity treatment networks </span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\">Support the commercial team and HCPs with knowledge building around the efficacy and safety of our product including AE/PV reporting.</span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Play a pivotal role in establishing appropriate multidisciplinary care including patient support programs</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Play a pivotal role in identifying hurdles and solutions in order to optimize patient identification and referral pathways.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Communicate key medical insights from KEEs and others to inform medical strategy</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Collaborate effectively across internal stakeholders (including Medical Affairs, Commercial and others) to ensure aligned execution, consistent communication, and compliance with company, legal, and regulatory requirements; contribute to Customer Relationship Management (CRM) documentation as appropriate.</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Respond to unsolicited requests for medical information in a timely manner. Ensure that an accurate and fair-balanced response is provided</span></span></span></span></span></span></span></li></ul><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Qualifications and Skills</span></span></b></span></span></span></span><ul><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Advanced degree in a pharmaceutical, scientific, or medical field (PharmD, PhD, MD) </span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">8 or more years’ experience within a Medical Science Liaison or similar field facing role with primary emphasis on field based scientific exchange within the biopharmaceutical industry.  Relevant pharmaceutical and clinical/therapeutic experience also a consideration</span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Rare diseases experience is a plus</span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\">Launch experience is a plus</span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Cross-functional mindset focused on a seamless collaboration with the commercial team</span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Excellent communication and presentation skills - fluent in local language for the market and in verbal and written English</span></span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Demonstrated knowledge of regional/local specific healthcare systems, the evolving medical landscape, reimbursement and industry trends. </span></span></span></span></span></span></li><li style=\"margin-left:32px;\"><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><span lang=\"en-us\" style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Ability to work in collaboration with the international region and with a positive attitude.</span></span></span></span></span></span></li></ul><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#4472c4;\">This role is field- based in Italy.  Candidates applying must be willing and able to work primarily out of their home office. This role will involve up to 50% travel.</span></span></span></i></span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#4472c4;\">The expected salary range for this position is € 70 000 – € 105 000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units. </span></span></span></i></span></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"><strong>More About Rhythm</strong><br>We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare melanocortin-4 receptor (MC4R) pathway diseases by rapidly advancing care and precision medicines that address the root cause.  Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.</span></span></i></span></span></span></span><br><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">At Rhythm Our Core Values Are</span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•     We are committed to advancing scientific understanding to improve patients’ lives</span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•     We are inspired to tackle tough challenges and have the courage to ask bold questions</span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•     We are eager to learn and adapt</span></span></span></span></i></span></span></span><br><span style=\"font-size:12pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span lang=\"en-us\" style=\"font-size:10pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">•     We believe collaboration and ownership are foundational for our success<br>•     </span></span></span></span></i></span></span></span><i style=\"font-family:Aptos, sans-serif;font-size:12pt;\"><span lang=\"en-us\" style=\"font-size:10pt;\"><span><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">We value the unique contribution each individual brings to furthering our mission</span></span></span></span></i><br><br> ",
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