Medical Science Liaison - New England

Posted 17 days agoViewed

💎 Seniority level: Middle, 3+ years

📍 Location: United States

🔍 Industry: Biotech

🗣️ Languages: English

⏳ Experience: 3+ years

🪄 Skills: Data AnalysisCommunication SkillsPresentation skillsResearch

3+ years of related experience in an MSL role in the pharmaceutical or biotech industry is highly preferred.
10+ years relevant clinical or pharmaceutical/biotech experience
Oncology therapeutic experience required.
Drug launch experience preferred.
Strong scientific knowledge as well as excellent presentation and teaching skills
Ability to interpret and communicate scientific data to various audiences.
Able to prioritize and manage several projects simultaneously.
Ability to work independently in a fast-paced and ever-changing environment.
Proven ability to develop external relationships with scientific experts.
Excellent oral and written communication skills
Ability to comply with all credentialing requirements for any healthcare institution which is part of the MSL territory, including, among other things, routine background checks, medical testing (i.e., Tuberculosis test) or proof of immunizations, training on facility policies, and adherence to confidentiality and/or HIPPA agreements.
Valid driver’s license with a clean driving record.
Ability to travel frequently (up to 60% of time), including the ability to travel overnight and occasionally on weekends.

Establish and maintain credible peer-to-peer scientific relationships with national, regional, and local opinion leaders in addition to other health care providers.
Develop strategic engagement plans in support of the overall medical affairs plan.
Deliver scientifically accurate, balanced, and unbiased medical and scientific presentations to stakeholders, healthcare providers, and patient groups.
Attend scientific conferences to collect and report relevant scientific and clinical data.
Assist with Arvinas-sponsored clinical trials and drug development activities.
Compliantly facilitate the submission and review of investigator-sponsored research proposals
Serve as a resource of clinical and scientific information for internal cross-functional partners.
Capture, analyze, and share insights from various external engagement activities (e.g., scientific expert, investigator, HCP, and payer interactions)
Respond to unsolicited requests for medical information.
Provide input into medical strategy for pipeline compounds.
Ensure and maintain compliance with all company policies, laws, industry, and regulatory requirements.