Home › Companies › Hbap Fa Us1 Oraclecloud Com CX 1 › Vice President, Head of Life Cycle Management
Vice President, Head of Life Cycle Management
Hbap Fa Us1 Oraclecloud Com CX 1 · Waltham, MA, United States · Active · $360,000–$420,000 / year · Oracle Recruiting Cloud / Fusion HCM
Job facts
| Field | Value |
|---|---|
| Company | Hbap Fa Us1 Oraclecloud Com CX 1 |
| Title | Vice President, Head of Life Cycle Management |
| Normalized title | - |
| Department / team | Research and Development |
| Location | Waltham, MA, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | $360,000–$420,000 / year |
| Status | active |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
| Posted / first seen | 2025-12-08 / 2026-05-31 |
| Changed / last seen | 2026-05-31 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Hbap Fa Us1 Oraclecloud Com CX 1. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Oracle Recruiting Cloud / Fusion HCM. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Waltham. | Open |
| Department jobs | Active postings in Research and Development. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Hbap Fa Us1 Oraclecloud Com CX 1 |
| Source | c9a1af55-d1aa-41d7-bb8e-0bf8dc082d85 |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
Description
Description
Reporting directly to the Head of Medical Affairs, the VP, Head of Life Cycle Management (LCM) is a highly visible and business-critical role at Alkermes. This role is tasked with understanding the business strategies and drivers underlying our medicines for the treatment of serious mental illness, sleep disorders and our emerging neuroscience pipeline and translating those drivers into data generation plans across our programs and disease areas of interest. This individual will need to effectively collaborate and communicate with colleagues within Medical Affairs and key cross-functional partners (e.g., Commercial, Clinical Development, Clinical Operations, Regulatory Affairs, Safety, Biostatistics, Program Management, Government Affairs, Business Development), and frequently represent the function to senior management and the company to healthcare professionals.
This position is based in Waltham, MA.
Responsibilities
Lead the efforts to collaborate with key cross-functional partners to define and implement comprehensive lifecycle management strategies for our marketed products and pipeline programs.
Analyze and interpret scientific data, disease/treatment landscape, and external stakeholder evidence to identify challenges, opportunities, and strategic imperatives to communicate and demonstrate our portfolio value.
Develop and execute data generation plans consistent with program goals, including leading Phase IIIB/ Phase IV and investigator-initiated research
Manage post-approval regulatory activities, including sNDA submissions.
Contribute to regulatory interactions, ensuring strategic alignment and scientific rigor.
Develop and oversee global expanded access programs and plans for our pipeline products.
Partner with the Scientific and Medical Communications team on plan, review, and approve publications and scientific content.
Identify and develop collaborative relationships with key investigators, and key thought leaders globally. Attend and oversee clinical advisory boards and investigator meetings.
Collaborate with Health Outcomes Research and Patient Advocacy to ensure a patient-centric approach.
Represent the company externally within clinical and pharmaceutical industry forums and professional associations.
Develop and lead a high-performing LCM team to execute on the startup and monitor the progress of LCM studies.
In collaboration with the clinical operations team, oversee the operational execution to ensure that the programs meet their timelines, budgets, and quality standards.
Manage study and departmental budgets in collaboration with project management and finance teams; ensure administrative compliance.
Ensure that standard operating procedures (SOP) for Clinical Development facilitate the development of effective clinical research protocols and are compliant with clinical/medical and industry standards.
Qualifications
MD with strong track record of minimum of 15 years of relevant biopharmaceutical industry experience required, at least 5 years of which should be managing LCM studies within clinical development and/or medical affairs.
Experience running and managing Phase IIIb/IV research programs and end to end LCM studies.
Proven track record successfully filing sNDA programs.
Operational experience of building and managing a team overseeing LCM studies.
Sleep/Neuroscience/Psychiatry therapeutic experience is a benefit, as is relevant clinical care experience.
Highly motivated self-starter who can work independently, manage complex issues, and relate to multiple internal and external stakeholders.
Experience working in a highly matrixed team environment and ability to lead through influence people across the organization and at all vertical levels.
Proven record of problem solving, excellent communication skills (written and verbal), and experience interacting with and presenting to senior management and key external stakeholders.
Experience building and managing teams and developing others.
Working knowledge of regulatory and compliance requirements.
Travel: Willingness/ability to travel up to 25% domestically. International travel may be required.
The annual base salary for this position ranges from $360,000 to $420,000. In addition, this position is eligible for an annual performance pay bonus. Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package. Additional details can be found on our careers website: www.alkermes.com/careers#working-here
#LI-MB1
Company
Why join Team Alkermes?
Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.
We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.
Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.
Full job record
| Job ID | 8dac8fe06920c6aa5876ddbba5033af685450edd |
| Org ID | d831e3c2-6a79-44af-a2cf-903b76ab4731 |
| Source ID | c9a1af55-d1aa-41d7-bb8e-0bf8dc082d85 |
| Board ID | c9a1af55-d1aa-41d7-bb8e-0bf8dc082d85 |
| Provider | oracle_hcm |
| Provider Job Key | 13771 |
| Title | Vice President, Head of Life Cycle Management |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Waltham, MA, United States |
| Department | Research and Development |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | MA |
| City | Waltham |
| Salary Raw | Description Reporting directly to the Head of Medical Affairs, the VP, Head of Life Cycle Management (LCM) is a highly visible and business-critical role at Alkermes. This role is tasked with understanding the business strategies and drivers underlying our medicines for the treatment of serious mental illness, sleep disorders and our emerging neuroscience pipeline and translating those drivers into data generation plans across our programs and disease areas of interest. This individual will need to effectively collaborate and communicate with colleagues within Medical Affairs and key cross-functional partners (e.g., Commercial, Clinical Development, Clinical Operations, Regulatory Affairs, Safety, Biostatistics, Program Management, Government Affairs, Business Development), and frequently represent the function to senior management and the company to healthcare professionals. This position is based in Waltham, MA. Responsibilities Lead the efforts to collaborate with key cross-functional partners to define and implement comprehensive lifecycle management strategies for our marketed products and pipeline programs. Analyze and interpret scientific data, disease/treatment landscape, and external stakeholder evidence to identify challenges, opportunities, and strategic imperatives to communicate and demonstrate our portfolio value. Develop and execute data generation plans consistent with program goals, including leading Phase IIIB/ Phase IV and investigator-initiated research Manage post-approval regulatory activities, including sNDA submissions. Contribute to regulatory interactions, ensuring strategic alignment and scientific rigor. Develop and oversee global expanded access programs and plans for our pipeline products. Partner with the Scientific and Medical Communications team on plan, review, and approve publications and scientific content. Identify and develop collaborative relationships with key investigators, and key thought leaders globally. Attend and oversee clinical advisory boards and investigator meetings. Collaborate with Health Outcomes Research and Patient Advocacy to ensure a patient-centric approach. Represent the company externally within clinical and pharmaceutical industry forums and professional associations. Develop and lead a high-performing LCM team to execute on the startup and monitor the progress of LCM studies. In collaboration with the clinical operations team, oversee the operational execution to ensure that the programs meet their timelines, budgets, and quality standards. Manage study and departmental budgets in collaboration with project management and finance teams; ensure administrative compliance. Ensure that standard operating procedures (SOP) for Clinical Development facilitate the development of effective clinical research protocols and are compliant with clinical/medical and industry standards. Qualifications MD with strong track record of minimum of 15 years of relevant biopharmaceutical industry experience required, at least 5 years of which should be managing LCM studies within clinical development and/or medical affairs. Experience running and managing Phase IIIb/IV research programs and end to end LCM studies. Proven track record successfully filing sNDA programs. Operational experience of building and managing a team overseeing LCM studies. Sleep/Neuroscience/Psychiatry therapeutic experience is a benefit, as is relevant clinical care experience. Highly motivated self-starter who can work independently, manage complex issues, and relate to multiple internal and external stakeholders. Experience working in a highly matrixed team environment and ability to lead through influence people across the organization and at all vertical levels. Proven record of problem solving, excellent communication skills (written and verbal), and experience interacting with and presenting to senior management and key external stakeholders. Experience building and managing teams and developing others. Working knowledge of regulatory and compliance requirements. Travel: Willingness/ability to travel up to 25% domestically. International travel may be required. The annual base salary for this position ranges from $360,000 to $420,000. In addition, this position is eligible for an annual performance pay bonus. Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package. Additional details can be found on our careers website: www.alkermes.com/careers#working-here #LI-MB1 Company Why join Team Alkermes? Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders. We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer. |
| Salary Min | 360,000 |
| Salary Max | 420,000 |
| Salary Currency | USD |
| Salary Period | year |
| Source URL | https://hbap.fa.us1.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/13771 |
| Apply URL | https://hbap.fa.us1.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/13771 |
| First Seen At | 2026-05-31 18:10:58Z |
| Last Seen At | 2026-06-06 11:11:22Z |
| Last Checked At | 2026-06-06 11:11:22Z |
| Last Changed At | 2026-05-31 18:10:58Z |
| Inactive At | — |
| Source Posted At | 2025-12-08 19:46:36Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=hbap.fa.us1.oraclecloud.com|CX_1/date=2026-06-06/2026-06-06T11-11-16-535Z-17c3bce20012c43cd6dd6a420957faaa6610803a2a194c866b3ecf324160566d.json |
Event Fields
{
"content_hash": "28b16b3061383cce72582e10c30f63c3f90c089a3af226fd9274025d493b039d",
"source_hash": "bf952b87fcfc2448c68a7dd6b23f04506b66d125a3b80ae509307e0880329a95",
"last_changed_at": "2026-05-31T18:10:58.917Z",
"active_status": "active"
}Parsed Structured
{
"language": "en",
"location": {
"raw": "Waltham, MA, United States",
"city": "Waltham",
"region": "MA",
"country": "United States",
"is_remote": false,
"confidence": 0.8
},
"salary_max": 420000,
"salary_min": 360000,
"inferred_at": "2026-06-06T11:11:22.953Z",
"launch_scope": {
"reason": "english_us_canada",
"included": true,
"language": "en",
"location": {
"raw": "Waltham, MA, United States",
"city": "Waltham",
"region": "MA",
"country": "United States",
"is_remote": false,
"confidence": 0.8
},
"countries": [
"United States"
]
},
"remote_policy": null,
"salary_period": "year",
"workplace_type": null,
"salary_currency": "USD"
}Extensions
{}Native Structured
{
"detail": {
"Id": "13771",
"Title": "Vice President, Head of Life Cycle Management",
"media": [],
"skills": [],
"JobType": null,
"Category": "Research and Development",
"JobGrade": null,
"JobLevel": null,
"JobShift": "First",
"WorkDays": null,
"WorkHours": null,
"WorkYears": null,
"Department": null,
"HotJobFlag": false,
"StudyLevel": "MD",
"WorkMonths": null,
"WorkerType": null,
"GeographyId": 300000032024578,
"JobFamilyId": 300000147605215,
"JobFunction": "Medical Affairs",
"JobSchedule": "Full time",
"BusinessUnit": null,
"ContractType": null,
"Organization": null,
"TrendingFlag": false,
"workLocation": [
{
"Country": null,
"Region1": null,
"Region2": null,
"Region3": null,
"Building": null,
"Latitude": "",
"Longitude": "",
"LocationId": null,
"PostalCode": null,
"TownOrCity": null,
"AddressLine1": null,
"AddressLine2": null,
"AddressLine3": null,
"AddressLine4": null,
"LocationName": null
}
],
"ContentLocale": "en",
"HiringManager": null,
"LegalEmployer": null,
"RequisitionId": 300001025597044,
"WorkplaceType": "",
"BusinessUnitId": 100000000170392,
"OrganizationId": 300000155417114,
"GeographyNodeId": 100000142475907,
"JobFunctionCode": "MEDICAL",
"LegalEmployerId": 300000001067001,
"PrimaryLocation": "Waltham, MA, United States",
"RequisitionType": "Professional",
"NumberOfOpenings": null,
"WorkplaceTypeCode": null,
"BeFirstToApplyFlag": false,
"otherWorkLocations": [],
"secondaryLocations": [],
"ExternalContactName": null,
"ShortDescriptionStr": "",
"ExternalContactEmail": null,
"ExternalPostedEndDate": null,
"OtherRequisitionTitle": null,
"requisitionFlexFields": [],
"ApplyWhenNotPostedFlag": null,
"DomesticTravelRequired": null,
"ExternalDescriptionStr": "<p>Reporting directly to the Head of Medical Affairs, the VP, Head of Life Cycle Management (LCM) is a highly visible and business-critical role at Alkermes. This role is tasked with understanding the business strategies and drivers underlying our medicines for the treatment of serious mental illness, sleep disorders and our emerging neuroscience pipeline and translating those drivers into data generation plans across our programs and disease areas of interest. This individual will need to effectively collaborate and communicate with colleagues within Medical Affairs and key cross-functional partners (e.g., Commercial, Clinical Development, Clinical Operations, Regulatory Affairs, Safety, Biostatistics, Program Management, Government Affairs, Business Development), and frequently represent the function to senior management and the company to healthcare professionals. </p><p>This position is based in Waltham, MA.</p>",
"ObjectVerNumberProfile": "1",
"PrimaryLocationCountry": "US",
"CorporateDescriptionStr": "<div>\n <div>\n <p><b>Why join Team Alkermes?</b></p>\n <p>Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.</p>\n <p></p>\n <p>We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. </p>\n </div>\n <div>\n <p>Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.</p>\n </div>\n</div>",
"ExternalPostedStartDate": "2025-12-08T19:46:36+00:00",
"ExternalQualificationsStr": "<ul style=\"list-style-type:disc;padding-left:31.67px;\"><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">MD with strong track record of minimum of 15 years of relevant biopharmaceutical industry experience required, at least 5 years of which should be managing LCM studies within clinical development and/or medical affairs.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Experience running and managing Phase IIIb/IV research programs and end to end LCM studies. </p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Proven track record successfully filing sNDA programs.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Operational experience of building and managing a team overseeing LCM studies.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Sleep/Neuroscience/Psychiatry therapeutic experience is a benefit, as is relevant clinical care experience.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Highly motivated self-starter who can work independently, manage complex issues, and relate to multiple internal and external stakeholders.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:23.25pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Experience working in a highly matrixed team environment and ability to lead through influence people across the organization and at all vertical levels.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Proven record of problem solving, excellent communication skills (written and verbal), and experience interacting with and presenting to senior management and key external stakeholders.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:0in;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Experience building and managing teams and developing others.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:0in;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Working knowledge of regulatory and compliance requirements.<br><br> </p></li></ul><p><strong>Travel: </strong>Willingness/ability to travel up to 25% domestically. International travel may be required.</p><p>The annual base salary for this position ranges from $360,000 to $420,000. In addition, this position is eligible for an annual performance pay bonus. Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package. Additional details can be found on our careers website: <a href=\"http://www.alkermes.com/careers\">www.alkermes.com/careers#working-here</a> <br><br>#LI-MB1</p>",
"InternalQualificationsStr": "<ul style=\"list-style-type:disc;padding-left:31.67px;\"><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">MD with strong track record of minimum of 15 years of relevant biopharmaceutical industry experience required, at least 5 years of which should be managing LCM studies within clinical development and/or medical affairs.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Experience running and managing Phase IIIb/IV research programs and end to end LCM studies. </p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Proven track record successfully filing sNDA programs.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Operational experience of building and managing a team overseeing LCM studies.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Sleep/Neuroscience/Psychiatry therapeutic experience is a benefit, as is relevant clinical care experience.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Highly motivated self-starter who can work independently, manage complex issues, and relate to multiple internal and external stakeholders.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:23.25pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Experience working in a highly matrixed team environment and ability to lead through influence people across the organization and at all vertical levels.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Proven record of problem solving, excellent communication skills (written and verbal), and experience interacting with and presenting to senior management and key external stakeholders.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:0in;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Experience building and managing teams and developing others.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:0in;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Working knowledge of regulatory and compliance requirements.<br><br> </p></li></ul><p><strong>Travel: </strong>Willingness/ability to travel up to 25% domestically. International travel may be required.</p><p>The annual base salary for this position ranges from $360,000 to $420,000. In addition, this position is eligible for an annual performance pay bonus. Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package. Additional details can be found on our careers website: <a href=\"http://www.alkermes.com/careers\">www.alkermes.com/careers#working-here</a> <br><br>#LI-MB1</p>",
"OrganizationDescriptionStr": "",
"primaryLocationCoordinates": [
{
"Latitude": "42.37649",
"Longitude": "-71.23502",
"CountryCode": "US",
"GeographyId": 300000032024578,
"GeographyNodeId": 100000142475907
}
],
"ExternalResponsibilitiesStr": "<ul style=\"list-style-type:disc;padding-left:31.67px;\"><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Lead the efforts to collaborate with key cross-functional partners to define and implement comprehensive lifecycle management strategies for our marketed products and pipeline programs.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Analyze and interpret scientific data, disease/treatment landscape, and external stakeholder evidence to identify challenges, opportunities, and strategic imperatives to communicate and demonstrate our portfolio value.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Develop and execute data generation plans consistent with program goals, including leading Phase IIIB/ Phase IV and investigator-initiated research</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Manage post-approval regulatory activities, including sNDA submissions.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Contribute to regulatory interactions, ensuring strategic alignment and scientific rigor.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Develop and oversee global expanded access programs and plans for our pipeline products.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Partner with the Scientific and Medical Communications team on plan, review, and approve publications and scientific content.</p></li><li><p style=\"background-color:white;text-autospace:ideograph-numeric ideograph-other;vertical-align:baseline;\">Identify and develop collaborative relationships with key investigators, and key thought leaders globally. Attend and oversee clinical advisory boards and investigator meetings. </p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Collaborate with Health Outcomes Research and Patient Advocacy to ensure a patient-centric approach.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Represent the company externally within clinical and pharmaceutical industry forums and professional associations.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Develop and lead a high-performing LCM team to execute on the startup and monitor the progress of LCM studies.</p></li><li><p style=\"background-color:white;text-autospace:ideograph-numeric ideograph-other;vertical-align:baseline;\">In collaboration with the clinical operations team, oversee the operational execution to ensure that the programs meet their timelines, budgets, and quality standards. </p></li><li><p style=\"background-color:white;text-autospace:ideograph-numeric ideograph-other;vertical-align:baseline;\">Manage study and departmental budgets in collaboration with project management and finance teams; ensure administrative compliance.</p></li><li><p style=\"background-color:white;text-autospace:ideograph-numeric ideograph-other;vertical-align:baseline;\">Ensure that standard operating procedures (SOP) for Clinical Development facilitate the development of effective clinical research protocols and are compliant with clinical/medical and industry standards. </p></li></ul>",
"InternalResponsibilitiesStr": "<ul style=\"list-style-type:disc;padding-left:31.67px;\"><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Lead the efforts to collaborate with key cross-functional partners to define and implement comprehensive lifecycle management strategies for our marketed products and pipeline programs.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Analyze and interpret scientific data, disease/treatment landscape, and external stakeholder evidence to identify challenges, opportunities, and strategic imperatives to communicate and demonstrate our portfolio value.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Develop and execute data generation plans consistent with program goals, including leading Phase IIIB/ Phase IV and investigator-initiated research</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Manage post-approval regulatory activities, including sNDA submissions.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Contribute to regulatory interactions, ensuring strategic alignment and scientific rigor.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Develop and oversee global expanded access programs and plans for our pipeline products.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Partner with the Scientific and Medical Communications team on plan, review, and approve publications and scientific content.</p></li><li><p style=\"background-color:white;text-autospace:ideograph-numeric ideograph-other;vertical-align:baseline;\">Identify and develop collaborative relationships with key investigators, and key thought leaders globally. Attend and oversee clinical advisory boards and investigator meetings. </p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Collaborate with Health Outcomes Research and Patient Advocacy to ensure a patient-centric approach.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Represent the company externally within clinical and pharmaceutical industry forums and professional associations.</p></li><li><p style=\"margin-bottom:.0001pt;margin-right:19.75pt;margin-top:0in;tab-stops:23.7pt 23.75pt;\">Develop and lead a high-performing LCM team to execute on the startup and monitor the progress of LCM studies.</p></li><li><p style=\"background-color:white;text-autospace:ideograph-numeric ideograph-other;vertical-align:baseline;\">In collaboration with the clinical operations team, oversee the operational execution to ensure that the programs meet their timelines, budgets, and quality standards. </p></li><li><p style=\"background-color:white;text-autospace:ideograph-numeric ideograph-other;vertical-align:baseline;\">Manage study and departmental budgets in collaboration with project management and finance teams; ensure administrative compliance.</p></li><li><p style=\"background-color:white;text-autospace:ideograph-numeric ideograph-other;vertical-align:baseline;\">Ensure that standard operating procedures (SOP) for Clinical Development facilitate the development of effective clinical research protocols and are compliant with clinical/medical and industry standards. </p></li></ul>",
"InternationalTravelRequired": null
},
"list_job": {
"Id": "13771",
"Title": "Vice President, Head of Life Cycle Management",
"JobType": null,
"Distance": 1765152000000,
"JobShift": null,
"Language": "US",
"WorkDays": null,
"JobFamily": null,
"Relevancy": 2,
"WorkHours": null,
"Department": null,
"HotJobFlag": false,
"PostedDate": "2025-12-08",
"StudyLevel": null,
"WorkerType": null,
"GeographyId": 300000032024578,
"JobFunction": null,
"JobSchedule": null,
"BusinessUnit": null,
"ContractType": null,
"ManagerLevel": null,
"Organization": null,
"TrendingFlag": false,
"workLocation": [
{
"Country": null,
"Region1": null,
"Region2": null,
"Region3": null,
"Building": null,
"Latitude": null,
"Longitude": null,
"LocationId": null,
"PostalCode": null,
"TownOrCity": null,
"AddressLine1": null,
"AddressLine2": null,
"AddressLine3": null,
"AddressLine4": null,
"LocationName": null
}
],
"LegalEmployer": null,
"MediaThumbURL": null,
"WorkplaceType": "",
"BusinessUnitId": 100000000170392,
"OrganizationId": 300000155417114,
"PostingEndDate": null,
"LegalEmployerId": 300000001067001,
"PrimaryLocation": "Waltham, MA, United States",
"WorkDurationYears": null,
"WorkplaceTypeCode": null,
"BeFirstToApplyFlag": false,
"WorkDurationMonths": null,
"otherWorkLocations": [],
"secondaryLocations": [],
"ShortDescriptionStr": "",
"requisitionFlexFields": [],
"DomesticTravelRequired": null,
"PrimaryLocationCountry": "US",
"ExternalQualificationsStr": null,
"ExternalResponsibilitiesStr": null,
"InternationalTravelRequired": null
},
"detail_meta": {
"url": "https://hbap.fa.us1.oraclecloud.com/hcmRestApi/resources/latest/recruitingCEJobRequisitionDetails?expand=all&onlyData=true&finder=ById;Id=%2213771%22,siteNumber=CX_1",
"http_status": 200,
"content_type": "application/json",
"response_bytes": 18975
},
"detail_errors": []
}Get this page with API
Rendered from the bluedoor Job Postings API. Reproduce it:
GET https://api.bluedoor.sh/job-postings/v1/jobs/8dac8fe06920c6aa5876ddbba5033af685450edd?include=descriptionJSONGET https://api.bluedoor.sh/job-postings/v1/orgs/d831e3c2-6a79-44af-a2cf-903b76ab4731JSONGET https://api.bluedoor.sh/job-postings/v1/sources/c9a1af55-d1aa-41d7-bb8e-0bf8dc082d85JSONGET https://api.bluedoor.sh/job-postings/v1/jobs/8dac8fe06920c6aa5876ddbba5033af685450edd/eventsJSON