Director, Medical Evidence Generation - Clinical Trial Physician, Cell Therapy

We need to output HTML fragment with sections for headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. We must not repeat job title as heading. Must not include Job ID/requisition numbers as headings; can fold minor metadata into short p or drop. We need to extract content: The posting includes a purpose paragraph, position summary, responsibilities (list of duties), qualifications & experience, compensation overview (pay), benefits, location/travel, etc. Also schedule? Not explicit schedule; maybe travel 20-30% globally. Not schedule specifics. So we may not include Schedule section unless specific schedule info present (like full-time, etc). The posting mentions full-time employees (FTE). Could include Schedule as full-time? But it's not explicit schedule like "Monday-Friday". Might be considered schedule info. The instruction: never create Pay/Schedule/Benefits sections unless posting actually states them. It does state compensation overview (pay) and benefits. Schedule? It mentions "expected travel » 20%-30% globally." That's not schedule. It also says full-time employees (FTE). Could interpret schedule as full-time. But it's not a schedule description like "40 hours per week". Might be okay to include Schedule with "Full-time". However instruction: never emit a heading followed by filler/placeholder text (e.g., "commensurate with experience", "not specified", "N/A", "varies", "TBD"). Full-time is not filler. Could include. But we need to decide: include Schedule section with "Full-time". The posting says "The starting pay range(s) listed above is for full-time employees (FTE)." So we can infer schedule is full-time. That's specific enough. Now we need to produce sections: - About the role: maybe the purpose paragraph and position summary? Could combine. Use

About the role

then

with purpose and summary. - Responsibilities: list of duties from "Provide medical/clinical accountability..." etc. Use

• . - Requirements: maybe location and travel? Or "Qualifications & Experience" is qualifications. Requirements could be "MD required..." etc. But we have Qualifications & Experience section. Could treat that as Qualifications. Requirements maybe "Established strategic leadership experience serving at least 5-10 years..." etc. Actually that is qualifications. We'll need to map. We have sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We need to decide what goes where. Let's extract: Purpose paragraph: "At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it." Position Summary: "This Director, Medical Evidence Generation (MEG) Clinical Trial Physician (CTP) - Cell Therapy (CT) role in Medical Affairs manages the evidence generation for the CT portfolio (including Medical Affairs Sponsored studies [MAST]) and provides clinical support for other studies in the MEG book of work (BOW). In this role, he/she will serve as the primary source of medical/clinical accountability and oversight for a MAST in alignment with the Integrated Evidence Plans (IEP) for the assets in Cell Therapy portfolio. He/she will work closely with Worldwide Medical (WWM) Cell Therapy Asset Lead, the MEG Cell Therapy Lead, and other members of the study team for the day-to-day oversight and conduction of the clinical studies included in the BOW for an asset in the Cell Therapy portfolio. The CT MEG CTP will lead and participate in cross-functional matrix leadership teams focused on building these relationships and actively sourcing research concepts that address critical evidence gaps for early and late assets being developed in prioritized indications. This role will report to the Cell Therapy MEG Lead and will be expected to:" Then list of responsibilities (starting with "Provide medical/clinical accountability and oversight..."). Thus About the role could combine purpose and position summary (excluding the list). Responsibilities will be the bullet list. Qualifications & Experience: includes many bullet-like sentences: "Established strategic leadership experience serving at least 5-10 years in a pharmaceutical industry setting and possessing an in-depth understanding of Clinical Development, Medical Affairs, and Commercial functions related to the drug development process.MD required (or x-US equivalent) plus 2-3 years of clinical trial experience, either in industry or academic setting; expertise in drug development process and clinical research; experience with implementation and conduction of medical affairs-led studies and/or cell therapy clinical development desirable.Adeptness at building credibility with external investigators and collaborative partners competently balancing business and scientific acumen complemented by strong leadership behaviors, authenticity, agility, and an enterprise mindset.Demonstrated ability to develop and sustain a high-performing team along with a proven ability to successfully lead teams (including matrix colleagues)Demonstrated track record of leadership in a complex, matrix environment.Exceptional communication and interpersonal skills to influence decision-making at all levels of the organization." We could split into Requirements (maybe the experience years) and Qualifications (education, skills) and Skills (communication, leadership). But we need to follow instruction: only include sections when posting has real specific content. We can allocate: - Requirements: maybe "MD required (or x-US equivalent) plus 2-3 years of clinical trial experience, either in industry or academic setting; expertise in drug development process and clinical research; experience with implementation and conduction of medical affairs-led studies and/or cell therapy clinical development desirable." - Qualifications: "Established strategic leadership experience serving at least 5-10 years in a pharmaceutical industry setting and possessing an in-depth understanding of Clinical Development, Medical Affairs, and Commercial functions related to the drug development process." - Skills: "Adeptness at building credibility with external investigators and collaborative partners competently balancing business and scientific acumen complemented by strong leadership behaviors, authenticity, agility, and an enterprise mindset.Demonstrated ability to develop and sustain a high-performing team along with a proven ability to successfully lead teams (including matrix colleagues)Demonstrated track record of leadership in a complex, matrix environment.Exceptional communication and interpersonal skills to influence decision-making at all levels of the organization." But there is overlap. However we need to avoid filler. It's okay. Pay: compensation overview with ranges. Benefits: benefits paragraph. Schedule: maybe "Full-time" or "Full-time (FTE)" plus travel 20-30% globally. Could include travel as part of schedule? Not exactly schedule. But we can include schedule as "Full-time" and mention travel in responsibilities? Travel is not a responsibility but a condition. Could include in Schedule section: "Full-time position with expected travel 20%-30% globally." Now we need to strip boilerplate: cookie/navigation/legal/EEO/equal-opportunity/scam-warning, duplicated lines, application instructions. Remove sections like "How We Work", "Supporting People With Disabilities", "Candidate Rights", "Data Protection", etc. Also remove the Job ID line at end. We must preserve all substantive information. So we need to keep location list: "This Position is based at Princeton Pike, NJ; Giralda Farms, NJ; Boudry, Switzerland; or Warsaw, Poland; expected travel » 20%-30% globally." That's substantive; could be placed in About the role or Responsibilities? Probably About the role includes location. We'll include in About the role paragraph. Now produce HTML:

  About the role

  At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. This Director, Medical Evidence Generation (MEG) Clinical Trial Physician (CTP) - Cell Therapy (CT) role in Medical Affairs manages the evidence generation for the CT portfolio (including Medical Affairs Sponsored studies [MAST]) and provides clinical support for other studies in the MEG book of work (BOW). In this role, he/she will serve as the primary source of medical/clinical accountability and oversight for a MAST in alignment with the Integrated Evidence Plans (IEP) for the assets in Cell Therapy portfolio. He/she will work closely with Worldwide Medical (WWM) Cell Therapy Asset Lead, the MEG Cell Therapy Lead, and other members of the study team for the day-to-day oversight and conduction of the clinical studies included in the BOW for an asset in the Cell Therapy portfolio. The CT MEG CTP will lead and participate in cross-functional matrix leadership teams focused on building these relationships and actively sourcing research concepts that address critical evidence gaps for early and late assets being developed in prioritized indications. This role will report to the Cell Therapy MEG Lead and will be expected to: ... (but we moved responsibilities to list). Actually we should not include the colon and then list; we will list responsibilities separately. So About the role paragraph ends before the list. So we stop before "This role will report to the Cell Therapy MEG Lead and will be expected to:"? Actually that sentence introduces responsibilities. Better to cut off before that sentence. So About the role ends at "The CT MEG CTP will lead and participate in cross-functional matrix leadership teams focused on building these relationships and actively sourcing research concepts that address critical evidence gaps for early and late assets being developed in prioritized indications." Then we have responsibilities list. Thus About the role paragraph includes purpose, position summary up to that sentence. Now Responsibilities: list each duty after colon. List items: - Provide medical/clinical accountability and oversight for the various medical affairs-led sponsored studies (interventional and non-interventional), in alignment with the Integrated Evidence Plans (IEP) for the assets in company’s portfolio. - Collaborate with the TA Medical Lead, CT MEG Lead, Clinical Scientist (CS), and Global Trial Manager (GTM) for the development of the study protocol and ICF, authoring and providing medical input during protocol development. - Partner with Clinical Scientist (CS) and Global Trial Manager (GTM) to support executional delivery of studies (e.g., clinical database development, clinical data oversight, site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc.). - Hold responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives (if applicable). - Accountable for medical data review of trial data, including eligibility assessment and interpretation of trial data results. - Provide medical oversight and accountability for the study-related work conducted by external partners (CROs), particularly related to medical monitoring-related activities. - Provide continuous medical education in partnership with CTLs and T/A Medical Leads related to protocol-specific training (supporting the study team, investigators, CROs, and others). - Provide medical expertise during Study Steering Committees, Investigators’ Meetings, and other study-related meetings with external audiences. - Build relationships with principal investigators and other relevant external stakeholders. - Responsible for partnering closely with key stakeholders across Medical, including the Clinical Research Collaborations group, working on the cell therapy portfolio to ensure cohesiveness and one MEG voice. - Fulfill GCP and compliance obligations for clinical conduct and maintains all required training. - Employ strong business acumen and fiscal stewardship focused on driving reciprocal scientific value creation and allocate resources consistent with company priorities. Now Requirements: maybe MD required etc. We'll put:

  Requirements

  • MD required (or x-US equivalent) plus 2-3 years of clinical trial experience, either in industry or academic setting; expertise in drug development