Medical Science Liaison/Senior Medical Science Liaison - Oncology - Mid Atlantic

EVERSANA•Raleigh, NC

4h•$185,000 - $210,000

About The Position

The Medical Science Liaison/Senior Medical Science Liaison is a highly trained, field-based scientific expert in GU Oncology, specifically non-muscle invasive bladder cancer (NMIBC). The role engages healthcare professionals and scientific stakeholders in compliant, peer-to-peer scientific exchange concerning the evidence base, standards of care, clinical research, and the patient journey. Following regulatory, legal, corporate, and client guidelines, the MSL builds scientific relationships with external experts, healthcare practitioners, professional societies, research networks, and institutions involved in NMIBC diagnosis, treatment, and research. The MSL serves as a field-based scientific resource for the client and represents the client as a scientific expert in the assigned geography. The position requires maintaining expertise in GU Oncology and gene therapy, managing an assigned territory, and supporting Medical Affairs activities and internal teams as assigned. Travel is 50%, including overnight travel, as business needs require.

Requirements

Terminal or advanced clinical degree, such as PharmD, MD, DO, PhD, MSN, NP, or PA-C.
Demonstrated scientific, clinical, and business acumen, with strong presentation, communication, and relationship-building skills.
Ability to interpret, synthesize, and present complex scientific and clinical data to varied healthcare audiences.
Excellent written and oral communication skills, sound judgment, and commitment to compliant scientific exchange.
MSL-level experience: approximately two years of pharmaceutical experience, or more than five years of strong clinical/academic experience with substantial external stakeholder engagement.
Senior MSL-level experience: five or more years of MSL experience, including at least three years in oncology.
Travel requirement of 50%, including overnight travel, as business needs require.

Nice To Haves

Experience in a field-based role and effective collaboration in a matrixed, cross-functional environment.
Working knowledge of institutions, research networks, professional societies, and healthcare systems in the assigned geography.
Prior product launch, indication expansion, or lifecycle management experience, where relevant.
GU Oncology experience.
Experience with viral vectors and cell and gene therapies.

Responsibilities

Function as the primary field medical and scientific point of contact within the assigned geography.
Maintain current clinical and scientific expertise in the therapeutic area, disease state, standards of care, treatment landscape, and relevant evidence.
Conduct accurate, balanced, non-promotional, and compliant scientific exchange with external experts and healthcare professionals.
Develop and execute territory and external expert engagement plans, identifying and maintaining long-term scientific relationships.
Understand clinical protocols, trial outcomes, research procedures, and the evolving evidence base.
Conduct pre-launch or lifecycle scientific profiling to deepen product, disease, stakeholder, and institutional knowledge.
Profile priority accounts and institutions to understand patient care pathways, treatment protocols, referral patterns, access considerations, and emerging research.
Address and document unsolicited medical or scientific information requests using approved processes.
Support advisory boards, scientific meetings, congresses, medical booth activities, and other Medical Affairs initiatives as assigned.
Provide timely, objective field insights and scientific feedback to internal stakeholders through approved channels.
Collaborate compliantly with cross-functional partners while maintaining appropriate Medical and Commercial independence and firewalls.
Support company-sponsored research sites and investigators, and serve as a resource for investigator-initiated research proposals, as assigned.
Provide medical support, clinical input, and scientific training to internal teams as requested and approved.
Manage the assigned territory, maintain required documentation, and contribute to team and organizational objectives.
Adhere to corporate policies, standard operating procedures, and applicable legal, regulatory, privacy, and compliance requirements.
Maintain subject-matter expertise in GU Oncology and gene therapy.
Represent the client as a field-based scientific expert.