What are the responsibilities and job description for the Medical Science Liaison Biosimilars - Southeast position at Fresenius Kabi USA, LLC?
Job Summary
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Join Fresenius Kabi as a Medical Science Liaison - Biosimilars.
Medical Science Liaisons (MSLs) are trained healthcare professionals whose primary role is to exchange scientific and medical information between the Company and the medical community. MSLs are responsible for cultivating and maintaining relationships with healthcare professionals and providing scientific support for Company products. MSLs must maintain scientific expertise and knowledge of clinical applications of Company products and medical treatment guidelines. MSLs must remain current on clinical knowledge and must be able to communicate complex medical and scientific concepts to a broad range of audiences. MSLs are field-based members of the Biosimilars medical affairs team.
This position will cover the Southeast territory for our oncology and immunology biosimilar product portfolio. The ideal candidate will live in or near a major airport in the southeast region of the USA.
Responsibilities
- Establishes and maintains healthcare professional relationships with physicians and other clinicians to provide scientific exchange per predefined targets and objectives and to ensure the safe and effective use of Company products.
- Prepares and regularly updates educational materials and presentations to support scientific exchange externally related to Company products.
- Responds appropriately and timely to unsolicited requests for off-label product information in accordance with regulatory guidelines and Company policies.
- Provides appropriate medical and scientific support to healthcare professionals and investigators for publications and clinical trials related to Company products in support of data generation and development of deeper medical and scientific understanding. Collaborates with Global Medical, Clinical, & Regulatory Affairs in the management of USA-based clinical trials, both internal and external.
- Evaluates clinical proposals of Investigator Initiated Trials for Company sponsorship in accordance with preestablished medical objectives and strategies, regulatory guidance, and Company policies.
- Provides training as required to internal company personnel.
- Collaborates with Global Vigilance Department and Global Quality & Compliance Department with respect to product adverse events and complaints per company procedures.
Requirements
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