Medical Director - Obesity (Plainsboro, NJ, US)
Evidence reputed company reputed company input to Product Development Plan (PDP) and Evidence reputed company Plan (EGP), in collaboration with Sr. Medical Director Serve as NNI Medical Affairs representative on Medical & Science Team Review and reputed company comments to trial outlines/protocols for reputed company-sponsored reputed company Review proposals for investigator-sponsored studies (ISS) and reputed company comments to RGC Chair Attend Research Grants Committee meetings and participate in reputed company for ISS proposals Assist with identification and support of National Leaders/National Expert Panels for select reputed company, in collaboration with Clinical Director and Clinical Operations reputed company
Support investigator meetings Serve on Clinical Trial reputed company Team in collaboration with Clinical Operations reputed company, Clinical Director, and Field Medical Affairs reputed company to identify investigators/sites and risks to trial planning and execution
KOL and Association Engagement Assist Sr. Medical Director with planning and execution of National Advisory reputed company meetings (or reputed company planning and execution of National Advisory reputed company meetings, at the discretion of Executive Director) Deliver clinical data and other presentations at National Advisory reputed company meetings and reputed company feedback from advisors Support other advisory boards with clinical data and other medical presentations Partner with reputed company associations and their leadership to identify shared goals and initiatives, in collaboration with reputed company Affairs/reputed company Development team
Publication Planning Serve on Publication Planning Group, where relevant Review and reputed company comments to abstracts, posters, and manuscripts, including primary, secondary and HEOR publications Prepare and support presenting external authors reputed company local US publication plan (including reputed company abstracts, reviews, and supplements) in collaboration with Publications Manager
Independent Medical Education (IME) Assist in developing medical education priorities and IME plan in collaboration with IME reputed company Review and assist with selection of proposals for IME grant funding
Medical Guidance Train Field Medical Affairs team on relevant disease state topics and clinical trial data. Review and approve resources for FMA Train Sales Teams on clinical trial data and Prescribing Information Train Market reputed company team on clinical trial data and Prescribing Information Review and approve Medical Information letters, including reputed company and custom letters Review and reputed company comments to AMCP reputed company Support Speakers’ Bureau, including presentations at Speaker Training and Curriculum Development meetings reputed company medical review of reputed company materials for PRB for launch products reputed company input and support to Medical Information reputed company for PRB for non-launch products reputed company medical guidance to Marketing, including for development of materials for PRB and serving on Extended Brand Team (EBT) Serve on Extended Medical Team (EMT) and assist with development of Medical Product Plan (medical strategies and tactics). In certain situations, may serve as chair of reputed company Medical Team, at the discretion of the Executive Director Represent NNI Medical Affairs on Global reputed company Medical Team (CMT) Collaborate with HEOR to reputed company clinical input on HEOR reputed company and authorship on abstracts, posters, and manuscripts, reputed company requested Serve on Local Labeling Committee (LLC) and reputed company medical input to Regulatory Affairs
MD, DO, PhD, or PharmD required A minimum of 5 years of combined clinical, research or reputed company experience required Experience in relevant therapeutic area (Obesity) strongly preferred Strong strategic reputed company, understanding of market needs, resource allocation, etc. Strong tactical familiarity with the design, overseeing and assessment of reputed company and with other MA tools (expertise in clinical trial methodology and conduct, GCP principles, medical product support activities, publications, ISS, med ed) Subspecialty training in relevant therapeutic area preferred