Role
- Medical Science Liaison (MSL/Sr. MSL) for US Medical Affairs Solid Tumor Gynecologic Oncology; field-based.
- Develop and enhance relationships with medical thought leaders to support Genmab approved and clinical-stage products.
- Provide scientific/clinical information via fair-balanced exchange; support new product launch excellence.
- Execute field medical activities with cross-functional teams to ensure differentiated customer experience and optimal patient outcomes.
- Territory: Southeast (Florida and Puerto Rico). Domestic travel ~50%.
Responsibilities
- Identify key thought leaders; establish and maintain HCP relationships in assigned territory.
- Develop and execute territory plans aligned with regional/national Medical Affairs strategies.
- Provide insights on emerging scientific/clinical data to improve value and appropriate use (compliant collaboration).
- Present clinical/scientific information to HCPs in response to unsolicited requests (as appropriate).
- Provide disease state and product medical/scientific education.
- Support product launches via HCP education for safe use.
- Serve as primary point of contact for investigator-sponsored trials (ISTs) from submission through activation/completion.
- Collaborate with cross-functional teams; drive engagement of HCPs in Genmab-sponsored trials.
- Maintain up-to-date knowledge of products, treatment trends, clinical trials, and gynecologic oncology scientific activities.
- Serve as a scientific resource to commercial partners (as appropriate).
- Support planning/execution of advisory boards.
- Represent Genmab at select medical/scientific conferences.
Requirements
- Advanced degree (PharmD, PhD, MD) strongly preferred; clinical background (NP/PA, etc.) and extensive oncology MSL experience considered.
- At least 2 years MSL/Medical Affairs experience in Oncology/Solid Tumor preferred.
- Strong knowledge/experience of healthcare and access environments.
- Ability to work independently and cross-functionally in a matrixed environment.
- Preferred: product launch experience or success as product/therapeutic point.
- Excellent communication/presentation, integrity, teamwork, and customer focus.
- Ability to organize/prioritize and work effectively in changing environments.
- Strong compliance knowledge; working knowledge of FDA, OIG, ICH, GCP, PhRMA Code, HIPAA, and relevant regulations.
- Technical acumen including MS Office; ability to adopt business applications.