Medical Director, US Medical Affairs, Prostate

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Medical Affairs Group

Job Sub Function:

Medical Affairs – MD

Job Category:

People Leader

All Job Posting Locations:

Horsham, Pennsylvania, United States of America

Job Description:

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

The Medical Director, Prostate Cancer will be accountable for delivering evidence-based medical leadership across the prostate program. This individual will represent Medical Affairs on cross-functional project teams, engage proactively with external experts and patient communities, and ensure high-quality medical input into clinical development, launch, and post-marketing activities. The role requires strong clinical judgment, clinical expertise and experience in oncology and medical affairs, and the ability to operate in a matrix environment

Key responsibilities

1. Strategic medical leadership

Define and drive the medical strategy for prostate cancer aligned with global program objectives and commercial strategy. Translate emerging science (tumor biology, biomarkers, resistance mechanisms) into actionable clinical hypotheses, trial concepts, and evidence plans. Prioritize medical and scientific questions and recommend resourcing to address critical evidence gaps.

2. Evidence generation & clinical support

Act as the primary contact for data generation initiatives, lead the development of the integrated evidence generation plan in response to emerging data and the changing competitive landscape. Oversee the development of scholarly publications from JNJ studies and collaborate on the strategic publication plan. Work collaboratively with Medical Directors, V&E team members, and other stakeholders. Prioritize evidence generation activities to support value-based research. Prepare and approve medical slide decks, white papers, and scientific materials for internal and external use.

3. External expert engagement

Identify, develop, and maintain relationships with key opinion leaders, academic investigators, and clinical societies in prostate oncology. Serve as the medical lead in advisory boards, lead data presentation and facilitate discussions to solicit feedback to inform the prostate medical strategy. Establish and foster relations with medical societies and patient advocacy organizations. 

4. Field medical enablement & MSL partnership

Support/ lead the development of medical education content for field medical and field V&E teams. Partner with MCSE teams on content development, review, and approval. Support content development, review, and approval of fair-balance advertising and promotional education content for commercial teams. 

5. Cross-functional collaboration & governance

Serve as the Medical Affairs representative on cross-functional teams (clinical development, regulatory, commercial, access/HEOR, legal). Provide medical review and approval for promotional medical content where appropriate and compliant.

Additional roles & responsibilities

Real-World Evidence & HEOR alignment: Partner closely with HEOR teams to design RWE studies that inform payer value dossiers and guideline adoption; translate RWE into clinical impact.

Guideline and payer engagement: Support efforts to shape clinical guideline inclusion and provide medical evidence to payer-facing teams.

Digital & omnichannel medical strategy: Contribute to digital engagement plans for medical education, scientific webinars, and virtual advisory activities.

Crisis and emergent scientific communications: Lead rapid medical response for urgent scientific, regulatory, or safety communications when needed.

Metrics & outcomes ownership: Define and monitor KPIs for medical activities (e.g., publication output, advisory board impact, MSL reach, study milestones), and report outcomes to leadership.

Qualifications:

• A MD degree is required.

• A background in Oncology and Prostate cancer experience is strongly preferred.

• Demonstrated experience in clinical trial design and clinical operations (Phases II–IV) within the pharmaceutical industry, CRO or Academia is required.

• A track record of scientific publications, presentations at major oncology meetings, or leadership in investigator collaborations is required.

• A minimum of five years of relevant experience in the pharmaceutical industry or equivalent experience is preferred

• Experience developing and executing medical launch strategies is preferred

• Experience developing congress strategies and prioritized KOL engagement is preferred

• Excellent written, oral and presentation skills are required

• Proven track record of developing, presenting and publishing clinical studies is preferred

• Strong organizational skills are a must

• A demonstrated ability to work in a matrix type environment with interaction with cross-functional teams is required.

• Willingness to travel up to 25% annually (domestic and international) is required.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

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Required Skills:

 

 

Preferred Skills:

Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Consulting, Developing Others, Healthcare Trends, Inclusive Leadership, Leadership, Medical Affairs, Medical Communications, Medical Compliance, Product Strategies, Representing, Research Proposals, Stakeholder Management, Strategic Thinking