Company: Large Pharmaceutical Company
Title: Associate Medical Director (Contract role)
Contract Position: 6 months with potential contract extension
Coordinates all clinical, medical, and regulatory activities linked to the interchangeable follow-on brands across CMR. Assist with the development of strategies to appropriately position the interchangeable follow-on brands as part of the Novo Nordisk portfolio.
This position reports directly to the Executive Director of Medical Affairs/CMRQ Manager of NNPI and will manage multiple internal relationships within Novo Nordisk Pharma Inc., Novo Nordisk Inc. CMR, and Global HQ. External relationships include healthcare professionals and other key customer groups.
- Coordinates with NNI CMR functions on all needs for the interchangeable follow-on brands and NNPI processes.
Responsible for oversight of all medical communications for the interchangeable follow-on brands.
Partners with Medical Information and Call Center colleagues to ensure all requests for medical information from healthcare professionals and patients related to the interchangeable follow-on brands are responded to with scientifically accurate information and in a timely manner.
Trains and supports the Field Medical Affairs team in relation to the interchangeable follow-on brands.
Coordinates with Regulatory Affairs on filings, monitoring of regulatory guidelines, and reporting to health authorities.
Coordinates with Safety on any safety reports and recalls related to the interchangeable follow-on brands.
Works with Quality function to ensure all relevant SOPs for NNPI in place.
Physical Requirements occasional overnight travel required
DEVELOPMENT OF PEOPLE
Development of People Not Applicable
An M.D. or D.O. and 2 years experience with clinical and prior direct patient care experience.
Research or pharmaceutical industry experience in the relevant therapeutic area preferred.
Strong cross-functional collaboration skills.
Superior communication skills.
Strong customer-centric mindset.
Strong strategic mindset, understanding of market needs, resource allocation, etc.
Strong tactical familiarity with the design, overseeing and assessment of clinical trials 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 endocrinology and metabolism preferred.
NOTES FROM THE MANAGER:
This is a new role that is being piloted, if this role works out, it may be extended; this role is to support Novo's new generic drugs; there may be an opportunity to work from home one or two days a week on occasion later next year
Job Type: Contract
- Health insurance
- Dental insurance
- Retirement plan