Manager, Laboratory and Sample Management

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  "detail": {
    "url": "https://rhythmpharmaceuticals.applytojob.com/apply/jobs/details/Kb2Ee2Vl5a?&",
    "heading": "Manager, Laboratory and Sample Management",
    "html_title": "JazzHR » Job Listings",
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    "description_html": "<span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-family:Calibri, sans-serif;\">Company Overview</span></b></span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-family:Calibri, sans-serif;\">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 adapt, learn, and our tenacity to overcome barriers, together.</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 style=\"font-family:Calibri, sans-serif;\">Opportunity Overview</span></b></span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#2b333a;\">As an integral member of the Clinical Operations team, the Manager, Laboratory and Sample Management will be responsible for sample management and laboratory processes within Clinical Operations, CROs and external vendors involved in clinical studies. This position will report to the Senior Director, Laboratory & Sample Management.</span></span></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 style=\"font-family:Calibri, sans-serif;\">Responsibilities and Duties</span></b></span></span></span></span><ul style=\"margin-bottom:1px;\"><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Day-to-day communication with external diagnostic programs, partner laboratories and CROs to ensure on-time delivery of samples and reporting of data across multiple projects.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Oversee clinical samples lifecycle management, including central laboratory third party laboratory, and long-term storage inventories to ensure sample holdings meet business and regulatory requirements.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Sample management and laboratory support of ongoing clinical studies.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Guiding internal rhythm data exchange, based on samples processed at diagnostic laboratories.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Support the creation and revision of lab related documents, both internal and site facing.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Proactive identification, mitigation, and resolution of lab and sample related issues.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Project management of ongoing clinical laboratory initiatives.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Support QA activities in auditing and troubleshooting external vendors.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Participation in quality and operational improvements within the company focused on external laboratory vendors.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Evaluate capabilities and qualifications of potential and contracted laboratory vendors based on portfolio needs.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Lab vendor Purchase Order (PO), Statement of Word (SOW), and invoice management.</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;\"><b><span style=\"font-family:Calibri, sans-serif;\">Qualifications and Skills</span></b></span></span></span></span><ul style=\"margin-bottom:1px;\"><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">BS or BA in a Life Science or related field.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Minimum of 5 years’ experience with CLIA/CAP accredited laboratories or CROs; MLS/MT (ASCP) certification preferred.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Regulatory knowledge, including Good Laboratory Practice (GLP) and Good Clinical Practice (GCP).</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Exceptional organizational skills and ability to deal with competing priorities, strong reasoning, and problem-solving ability.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Ability to assemble a plan and execute on the details.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Proficient with MS Office Suite (Excel, Word, and PowerPoint).</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Ability to communicate effectively with internal and external stakeholders.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Project Management experience preferable</span></span></span></span></span></span></li></ul><br><br><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:'Times New Roman', serif;\"><i><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#0070c0;\">This role is based out of our corporate office in Boston, Massachusetts. Rhythm operates in a hybrid-work model. Candidates applying must be willing and able to be in the Boston office in coordination with their department and business needs.</span></span></span></span></i><i><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#0070c0;\"> <span style=\"background:#FFFFFF;\">This role may involve some travel.</span></span></span></span></i></span></span></span><br><br><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:'Times New Roman', serif;\"><i><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#0070c0;\">The expected salary range for this position is $110,000 - $165,000. 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></span></i></span></span></span><br><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">More about Rhythm </span></span></i></b><br><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">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 neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism. </span></span></span></i><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"> </span></span></i></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">At Rhythm our core values are:</span></span></i></span></span></span><ul><li style=\"text-align:justify;margin-left:8px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">We are committed to advancing scientific understanding to improve patients’ lives</span></span></i></span></span></span></li><li style=\"text-align:justify;margin-left:8px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">We are inspired to tackle tough challenges and have the courage to ask bold questions</span></span></i></span></span></span></li><li style=\"text-align:justify;margin-left:8px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">We are eager to learn and adapt</span></span></i></span></span></span></li><li style=\"text-align:justify;margin-left:8px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">We believe collaboration and ownership are foundational for our success</span></span></i></span></span></span></li><li style=\"text-align:justify;margin-left:8px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">We value the unique contribution each individual brings to furthering our mission</span></span></i></span></span></span></li></ul><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">Rhythm is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service, or any other class protected by state or federal law. </span></span></i></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">Headquartered in Boston, Rhythm is proud to have been named one of the </span></span></i><span style=\"font-family:Calibri, sans-serif;\"><a href=\"https://www.bostonglobe.com/magazine/top-places-work/2023/\" style=\"color:#467886;text-decoration:underline;\"><i><span style=\"font-size:10pt;\">Top Places to Work</span></i></a></span><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"> in Massachusetts.</span></span></i></span></span></span>",
    "description_text": "Company Overview\n 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 adapt, learn, and our tenacity to overcome barriers, together.\n Opportunity Overview\n As an integral member of the Clinical Operations team, the Manager, Laboratory and Sample Management will be responsible for sample management and laboratory processes within Clinical Operations, CROs and external vendors involved in clinical studies. This position will report to the Senior Director, Laboratory & Sample Management.\n Responsibilities and Duties Day-to-day communication with external diagnostic programs, partner laboratories and CROs to ensure on-time delivery of samples and reporting of data across multiple projects.\n Oversee clinical samples lifecycle management, including central laboratory third party laboratory, and long-term storage inventories to ensure sample holdings meet business and regulatory requirements.\n Sample management and laboratory support of ongoing clinical studies.\n Guiding internal rhythm data exchange, based on samples processed at diagnostic laboratories.\n Support the creation and revision of lab related documents, both internal and site facing.\n Proactive identification, mitigation, and resolution of lab and sample related issues.\n Project management of ongoing clinical laboratory initiatives.\n Support QA activities in auditing and troubleshooting external vendors.\n Participation in quality and operational improvements within the company focused on external laboratory vendors.\n Evaluate capabilities and qualifications of potential and contracted laboratory vendors based on portfolio needs.\n Lab vendor Purchase Order (PO), Statement of Word (SOW), and invoice management.\n Qualifications and Skills BS or BA in a Life Science or related field.\n Minimum of 5 years’ experience with CLIA/CAP accredited laboratories or CROs; MLS/MT (ASCP) certification preferred.\n Regulatory knowledge, including Good Laboratory Practice (GLP) and Good Clinical Practice (GCP).\n Exceptional organizational skills and ability to deal with competing priorities, strong reasoning, and problem-solving ability.\n Ability to assemble a plan and execute on the details.\n Proficient with MS Office Suite (Excel, Word, and PowerPoint).\n Ability to communicate effectively with internal and external stakeholders.\n Project Management experience preferable\n This role is based out of our corporate office in Boston, Massachusetts. Rhythm operates in a hybrid-work model. Candidates applying must be willing and able to be in the Boston office in coordination with their department and business needs. This role may involve some travel.\n The expected salary range for this position is $110,000 - $165,000. 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\n 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 neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.\n At Rhythm our core values are: 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\n Rhythm is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service, or any other class protected by state or federal law.\n Headquartered in Boston, Rhythm is proud to have been named one of the Top Places to Work in Massachusetts.",
    "jsonld_jobposting": {
      "url": "https://rhythmpharmaceuticals.applytojob.com/apply/Kb2Ee2Vl5a/Manager-Laboratory-And-Sample-Management",
      "@type": "JobPosting",
      "title": "Manager, Laboratory and Sample Management",
      "@context": "http://schema.org/",
      "datePosted": "2026-06-01",
      "description": "<span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><b><span style=\"font-family:Calibri, sans-serif;\">Company Overview</span></b></span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"font-family:Calibri, sans-serif;\">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 adapt, learn, and our tenacity to overcome barriers, together.</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 style=\"font-family:Calibri, sans-serif;\">Opportunity Overview</span></b></span></span></span></span><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span><span style=\"font-family:Aptos, sans-serif;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#2b333a;\">As an integral member of the Clinical Operations team, the Manager, Laboratory and Sample Management will be responsible for sample management and laboratory processes within Clinical Operations, CROs and external vendors involved in clinical studies. This position will report to the Senior Director, Laboratory & Sample Management.</span></span></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 style=\"font-family:Calibri, sans-serif;\">Responsibilities and Duties</span></b></span></span></span></span><ul style=\"margin-bottom:1px;\"><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Day-to-day communication with external diagnostic programs, partner laboratories and CROs to ensure on-time delivery of samples and reporting of data across multiple projects.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Oversee clinical samples lifecycle management, including central laboratory third party laboratory, and long-term storage inventories to ensure sample holdings meet business and regulatory requirements.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Sample management and laboratory support of ongoing clinical studies.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Guiding internal rhythm data exchange, based on samples processed at diagnostic laboratories.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Support the creation and revision of lab related documents, both internal and site facing.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Proactive identification, mitigation, and resolution of lab and sample related issues.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Project management of ongoing clinical laboratory initiatives.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Support QA activities in auditing and troubleshooting external vendors.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Participation in quality and operational improvements within the company focused on external laboratory vendors.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Evaluate capabilities and qualifications of potential and contracted laboratory vendors based on portfolio needs.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Lab vendor Purchase Order (PO), Statement of Word (SOW), and invoice management.</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;\"><b><span style=\"font-family:Calibri, sans-serif;\">Qualifications and Skills</span></b></span></span></span></span><ul style=\"margin-bottom:1px;\"><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">BS or BA in a Life Science or related field.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Minimum of 5 years’ experience with CLIA/CAP accredited laboratories or CROs; MLS/MT (ASCP) certification preferred.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Regulatory knowledge, including Good Laboratory Practice (GLP) and Good Clinical Practice (GCP).</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Exceptional organizational skills and ability to deal with competing priorities, strong reasoning, and problem-solving ability.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Ability to assemble a plan and execute on the details.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Proficient with MS Office Suite (Excel, Word, and PowerPoint).</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Ability to communicate effectively with internal and external stakeholders.</span></span></span></span></span></span></li><li style=\"margin-bottom:1px;margin-left:7px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:103%;\"><span style=\"font-family:Aptos, sans-serif;\"><span style=\"line-height:103%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">Project Management experience preferable</span></span></span></span></span></span></li></ul><br><br><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:'Times New Roman', serif;\"><i><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#0070c0;\">This role is based out of our corporate office in Boston, Massachusetts. Rhythm operates in a hybrid-work model. Candidates applying must be willing and able to be in the Boston office in coordination with their department and business needs.</span></span></span></span></i><i><span style=\"font-size:11pt;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#0070c0;\"> <span style=\"background:#FFFFFF;\">This role may involve some travel.</span></span></span></span></i></span></span></span><br><br><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:'Times New Roman', serif;\"><i><span style=\"font-size:11pt;\"><span style=\"background:#FFFFFF;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#0070c0;\">The expected salary range for this position is $110,000 - $165,000. 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></span></i></span></span></span><br><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><b><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">More about Rhythm </span></span></i></b><br><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"color:#000000;\">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 neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism. </span></span></span></i><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"> </span></span></i></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">At Rhythm our core values are:</span></span></i></span></span></span><ul><li style=\"text-align:justify;margin-left:8px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">We are committed to advancing scientific understanding to improve patients’ lives</span></span></i></span></span></span></li><li style=\"text-align:justify;margin-left:8px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">We are inspired to tackle tough challenges and have the courage to ask bold questions</span></span></i></span></span></span></li><li style=\"text-align:justify;margin-left:8px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">We are eager to learn and adapt</span></span></i></span></span></span></li><li style=\"text-align:justify;margin-left:8px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">We believe collaboration and ownership are foundational for our success</span></span></i></span></span></span></li><li style=\"text-align:justify;margin-left:8px;\"><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">We value the unique contribution each individual brings to furthering our mission</span></span></i></span></span></span></li></ul><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">Rhythm is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service, or any other class protected by state or federal law. </span></span></i></span></span></span><br><br><span style=\"font-size:11pt;\"><span style=\"line-height:normal;\"><span style=\"font-family:Aptos, sans-serif;\"><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\">Headquartered in Boston, Rhythm is proud to have been named one of the </span></span></i><span style=\"font-family:Calibri, sans-serif;\"><a href=\"https://www.bostonglobe.com/magazine/top-places-work/2023/\" style=\"color:#467886;text-decoration:underline;\"><i><span style=\"font-size:10pt;\">Top Places to Work</span></i></a></span><i><span style=\"font-size:10pt;\"><span style=\"font-family:Calibri, sans-serif;\"> in Massachusetts.</span></span></i></span></span></span>",
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