Medical Science Liaison (Central)

Role Summary

Medical Science Liaison (Central) located in the Central US. Engage with healthcare professionals to provide high-level scientific support for education and scientific exchange in oncology, supporting the development of novel bispecific antibody therapeutics. Reports to the Field Medical Director.

Responsibilities

• Support study start-up through review of competitive trial landscape and precedent trials; engage with prospective investigators and sites
• Expand knowledge of investigational sites to build a network including site capabilities and past performance
• Inform Clinical Operations when investigators express interest in becoming sites
• Develop and execute field medical affairs plan for the assigned territory aligned with medical affairs strategies
• Act as a liaison for clinical and scientific information exchange with regional oncologists, pathologists, oncology nurses, NPs, PAs and pharmacists
• Deliver high-quality education and awareness presentations to support optimal patient care
• Obtain, assimilate, organize and report field insights in a concise, clear, and compliant manner
• Provide timely, accurate, specific and balanced responses to professional information requests in collaboration with medical communications
• Provide complete and timely documentation of interactions and contacts
• Complete administrative reports such as expense and status reports in a timely manner
• Provide reports, assessments and HCP insights clearly and promptly
• Maintain and continually develop scientific knowledge of the relevant competitive landscape
• Attend and participate in compliance trainings
• Follow all applicable laws, regulations, and industry codes
• Attend national, regional and local conferences and symposia in line with company objectives
• Follow company policies and procedures applicable to collaborators and institutions

Qualifications

• M.D., Ph.D., Pharm.D. or NP/PA with appropriate clinical experience and scientific background
• 2+ years oncology clinical experience and 1+ years MSL experience in pharmaceutical industry
• Knowledge of pharmaceutical rules, regulatory law, guidelines and codes (e.g., PhRMA Code)
• Strong collaboration skills to coordinate efforts and accomplish goals as a team
• Ability to develop trust and maintain integrity with internal and external partners
• Demonstrated ability to achieve individual and team objectives
• Excellent interpersonal, verbal and written communication skills
• Ability to learn new scientific and technical information quickly
• Strong computer skills, proficiency in online data searches, MS Word, PowerPoint and Excel
• Ability to manage multiple assignments and meet deadlines in a fast-paced environment
• Travel approximately 50%

Education

• A degree corresponding to the clinical background above (M.D., Ph.D., Pharm.D. or NP/PA)

Additional Requirements

• Travel approximately 50% (car, plane, etc.)