The Opportunity: 

The Medical Science Liaison (MSL) is a field-based member of the Medical Affairs support team and will work closely with the Director, Medical Affairs. The MSL will apply scientific knowledge and experience to organize the collection of and analyze clinical data, and educate physicians. The MSL is responsible for establishing and maintaining clinical/scientific relationships with key opinion leaders, researchers, coordinators, laboratory managers, and other members of the scientific community.

• Establish and maintain scientific relationships with the key opinion leaders, researchers, coordinators, laboratory managers, and other members of the scientific community


• Provide timely and relevant updates, scientific support and responses to scientific or medical inquires related to products in conjunction with the Director, Medical Affairs


• Analyze, interpret, and clarify product results for scientific and medical publications and in connection with on-going studies and trials in coordination with clinicians and the Acting Director, Medical Affairs


• Interact regularly with senior product and clinical management for strategic development issues related to the scientific and clinical utility of the product


• Assist with the design of clinical study protocols


• Provide scientific support at medical meetings


• Coordinate and participate in scientific advisory board meetings


• Coordinate and manage activities related to investigator initiated studies with company products


• Provide management of publications and abstracts


• Function as a liaison in the resolution of reimbursement issues


• Maintain thorough up to date knowledge of disease state, clinical information, and product data

Required:

• Advanced degree in clinical science (PhD, Pharm D, MD, OMD)


•  3+ years in a clinical setting with a working knowledge of immunology, infectious disease or transplant


• Strong interpersonal skills 


• Able to work effectively in a team environment


• Able to analyze, interpret and evaluate clinical data and clinical scenarios


• Leadership ability to effectively manage projects


• Knowledge of FDA and other regulatory agency and professional requirements