Vacancy has expired
Show me jobs like this one| Job Ref: | 5824BR |
| State: | California (CA) |
| City: | Thousand Oaks |
| Job Description: |
Reporting to the Denosumab Medical Communications Director, the Sr. Manager is responsible for providing scientifically rigorous and high impact support of Scientific Affairs activities including medical content expertise for the brand teams. The position will support coordination and implementation of programs and materials that support global medical strategies for denosumab in the oncology and urology areas. Key responsibilities may include, but are not limited to, the following: providing clinical and strategic input to Global Development and Global Commercial Organizations; managing cross functional teams responsible for coordinating and implementing Medical Communications projects for the Oncology Therapeutic Area; providing clinical support of key scientific congresses and meetings; creating tools for Regional Medical Liaisons (RMLs); leading advisory boards; participating in task forces on competitive and market issues; managing budget and resources (including strategic vendors) associated with various projects; and reviewing field-based promotional and educational materials for appropriate interpretation of clinical data. Some travel required, usually 15% and occasionally up to 20%. Basic Qualifications:- PharmD, PhD, MD, DO (other Doctorate Degrees may be considered)- 3 or more years of Clinical Development and/or Medical Affairs experiencePreferred Qualifications:- 3 or more years of Clinical Development and/or Medical Affairs experience in a biotech or pharmaceutical company- Prior experience in Medical Affairs or Clinical Development within the biopharmaceutical industry, or clinical experience, in the areas of bone health, oncology or urology- Understanding of Medical Communications projects including disease state education programs, advisory boards, congress/publication plans and RML resources- Experience with commercial launch of new product - Experience with product (development/marketing) collaborations- Excellent written, oral, and presentation skills and the ability to critically analyze the scientific literature to form logical opinions- An understanding of the pharmaceutical commercialization process, and knowledge of the legal and regulatory guidelines affecting promotion of prescription products- The ability to work in teams and interface in a dynamic environment across corporate functions- Prior experience managing consultants and vendors is desired. RequirementsBasic Qualifications:- PharmD, PhD, MD, DO (other Doctorate Degrees may be considered)- 3 or more years of Clinical Development and/or Medical Affairs experience Preferred Qualifications:- 3 or more years of Clinical Development and/or Medical Affairs experience in a biotech or pharmaceutical company- Prior experience in Medical Affairs or Clinical Development within the biopharmaceutical industry, or clinical experience, in the areas of bone health, oncology or urology- Understanding of Medical Communications projects including disease state education programs, advisory boards, congress/publication plans and RML resources- Experience with commercial launch of new product |
| Company Name: | Amgen |
| Post Date: | 08/06/2010 |
