Group Medical Director, Medical Affairs (Prostate)

Johnson & Johnson, is recruiting for a Group Medical Director, Medical Affairs (Prostate) to be located in Horsham, PA.

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 https://www.jnj.com/.

The Group Medical Director, Medical Affairs (GMD) will have medical oversight of multiple indications/projects and/or products for the prostate area and potentially broader GU portfolio, reporting the Head Medical Affairs, Prostate TA (HMA, TA). The GMD Prostate may lead other Medical Directors to develop the medical strategy for assigned projects / products with a goal to address medical and scientific issues and to ensure the appropriate use of relevant Janssen Medical Affairs supported products. The medical strategy will be aligned with MA leadership and integrated evidence team leads (IETLs).

The GMD will have higher degree of autonomy in working with MA leadership to devise strategies addressing crucial gaps via critical relationships across Medical Affairs, Global Medical Affairs, R&D, V&E, Commercial and others. He/she will lead and effectively partner with Alliance partner (if applicable) on those activities. GMD may also work more broadly across GU and Solid Tumor portfolio.

Other Responsibilities include, but are not limited to the following:

• The GMD Prostate is responsible for securing funds for research budgets and elevate to supervisor, if required.
• Individually or through his/her MDs provides medical monitoring and medical oversight for company-sponsored Medical Affairs-led interventional and observational clinical trials
• Contributing to strategy around, approval of and implementation of Investigator Initiated Study (IIS) strategy as well as assessment and supervision of IIS conduct (as appropriate)
• Oversee the medical support in the development of compliant promotional materials and the training of product representatives and other internal and external stakeholders; supports Commercial functions appropriately.
• Develops and aligns Advisory Board strategy, executes Advisory Boards and maintains relationships with external investigators and opinion leaders.
• Ensures development of scholarly publications arising from Janssen studies
• Support the development of product monographs and responses to product inquiries