What are the responsibilities and job description for the Medical Director Oncology CART US Medical Affairs position at Johnson & Johnson?
Johnson & Johnson is recruiting for a Medical Director, CAR-T, US Medical Affairs. This role is located in Horsham, PA, but must support West Coast Business Hours (Pacific Time Zone). Remote work options may be considered on a case-by-case basis and if approved by the Company. This role may require up to 20% travel.
Skills, Experience, Qualifications, If you have the right match for this opportunity, then make sure to apply today.
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.
The Medical Director within US MAF, CAR-T leads team functions to support providers using CAR-T therapy to optimize patient experience and outcome. In this role, responsibilities include design, development and implementation of programs for CAR-T products related to post-marketing clinical trials, solicited and non-solicited studies and publications.
Duties and responsibilities include, but are not limited to :
- Lead team functions, coordinates the design and implements plans for the program.
- Ensures CAR-T medical affair's objectives are aligned with the goals and mission of the company.
- Reviews and approves educational, promotional and reporting materials for use by internal partners.
- Strategizes and prioritizes publication proposals.
- Serves as the project champion to ensure timeline adherence and project completion.
- Develops and provides input to research protocols for specific projects promoting company message and value.
- Assists in strategic development and is responsible for clinical trials, including protocol, staffing and budgeting as it relates to key initiatives.
- Develops policies and procedures for development.
- Develops plans for continuous improvement to build an environment in Medical Affairs that encourages and recognizes creativity, innovation, collaboration, risk-taking and empowerment that furthers product development.
- Directs budget management, contracting and oversight of vendor activities. Implements the company's drug surveillance / product safety program which includes following up on adverse reaction reports.
- Is a key clinical contact for commercial CAR-T questions, internally and externally.
- Provides solutions surrounding legal liability and compliance with government.
- Ensures strong cross-functional working relationship between Medical Affairs and internal partners to deliver timely and clinically relevant expertise to support product development.
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