Alnylam Pharmaceuticals

Develop, maintain, and execute US KOL and US Institution plans within respective geography. Collaborate with health care professionals to identify opportunities for the development of algorithms and guidelines to facilitate early diagnosis Provide in-depth drug mechanism of action and emerging clinical information to health care providers in the respective geography. Support the efforts of patient support groups and educational foundations. Provide medical and scientific input into the planning and execution of advisory boards and work with experts to review speaker presentations and provide additional medical background where requested. Contribute to Alnylam's achievement of Company objectives for pre-approved products. Provide educational meeting support at scientific congresses. Coordinate required medical, legal, and regulatory review and approval of all field documents for distribution or presentation. PhD, PharmD, DNP or MD with 3 to 5 years' industry experience. Proven clinical background to enable engagement of Health Care Professionals in a scientifically meaningful exchange. Prior experience in rare disease strongly preferred. Experience in clinical research, patient recruitment, and investigator-sponsored trials. Experience in medical education and KOL management. Effective communication of evidence based scientific information. Ability to work collaboratively and cross-functionally. Capable of managing shifting priorities in a rapidly changing and environment Decision-making and accountability. Clear alignment with Alnylam Core Values