Medical Science Liaison - Biosimilars

Job Summary

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 covers the West territory (CA, AZ, NM, TX, OK). Due to frequent travel, preference will be given to candidates living near a major airport, ideally California or Texas.

• Base salary range: $150,000-165,000.
• Position is eligible to participate in an annual bonus plan with a target of 14% of the base salary.
• Position is eligible for a fleet vehicle.
• Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
• Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.

Responsibilities

• Establish and maintain 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.
• Prepare and regularly update educational materials and presentations to support scientific exchange externally related to Company products.
• Respond appropriately and timely to unsolicited requests for off label product information in accordance with regulatory guidelines and Company policies.
• Provide 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. Collaborate with Global Medical, Clinical, & Regulatory Affairs in the management of USA based clinical trials, both internal and external.
• Evaluate clinical proposals of Investigator Initiated Trials for Company sponsorship in accordance with pre-established medical objectives and strategies, regulatory guidance and Company policies.
• Provide training as required to internal company personnel.
• Collaborate with Global Vigilance Department and Global Quality & Compliance Department with respect to product adverse events and complaints per company procedure.
• Job Requirements
• Advanced degree in a clinical or scientific discipline is required (e.g. Ph.D. with 5+ years of transferrable experience, MD with 5+ years of clinical experience, PharmD with 5+ years Pharmacy experience (could include residency experience), Advanced Practice Provider (Nurse Practitioners and Physician Assistant and Advanced Degree Registered Dietician) with 5+ years of clinical experience).
• 1+ years of experience as a Medical Science Liaison preferred.
• Pharmaceutical industry experience is preferred.
• Specialty pharmaceuticals experience with biological therapies and /or biosimilars is preferred.
• Knowledge of Immunology/Inflammation and/or Oncology .
• Demonstrated skill in interpreting and writing scientific documents.
• Excellent presentation and communication skills are mandatory – capacity to translate complex clinical information in concise verbal and written description.
• Demonstrated skills in communicating via virtual platforms and managing electronic shared databases.
• Knowledge of pharmaceutical product development and clinical trial design processes.
• Knowledge of US Healthcare system including reimbursement and access to pharmaceutical therapies.
• Knowledge of applicable regulatory, legal and compliance standards.
• The Company’s primary business language is English. The successful candidate must be able to effectively speak, read, write, and understand English to perform the essential functions of the position, including independently understanding policies, procedures, training materials, and workplace communications written in English due to our heavily regulated work environment.
• Position will require 40-50% travel, including overnight stays.  A valid US driver’s license and clean driving record are required.
• Additional Information
• We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability, 401K with company contribution, and wellness program.

Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is at‑will, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.