Senior Medical Science Liaison, CVRM Pipeline (West)
About the role
The Therapeutic Area Pipeline Medical Science Liaison (TA Pipeline MSL) is a field medical partner responsible for providing clinical, scientific, and other relevant information related to disease states and the appropriate utilization of Genentech medicines in the TA pipeline (and TA-related approved medicines, as appropriate).
Responsibilities
- Ensure end-to-end customer experience for TA specific customers in the region.
- Demonstrate deep scientific expertise in assigned molecules/products and therapeutic areas to exchange relevant information with thought leaders and healthcare decision makers.
- Aid with Phase I - IV sponsored and supported clinical trials, health economic outcomes research, other TA specific medical collaborations; provide clinical expertise overview of performance metrics and feedback regarding operational management of clinical trials to ensure optimal site selection and performance.
- Supports start-up, recruitment, and retention in assigned geographies. Provides critical collaboration with CRO personnel, as appropriate, and in pre-specified manner.
- Build and leverage relationships with key external scientific and medical customers to understand evolving healthcare trends.
- Continuous learning within the therapeutic area, active participation in upskilling programs, and adherence to guidelines and procedures.
Requirements
- Advanced Clinical/Science Degree (e.g., MD, PharmD, PhD, MSN, NP, PA etc.).
- BSN with extensive field medical experience with a pharmaceutical company.
- Minimum of 5 years related work experience (clinical, managed care, or industry experience).
- Proficiency in GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use).
- Relevant therapeutic area knowledge, comprehensive understanding of product and safety profiles, and familiarity with managed care, health economics, reimbursement, and legal and regulatory landscape in the pharmaceutical/biotechnology industry.
Qualifications
- Advanced Clinical/Science Degree (e.g., MD, PharmD, PhD, MSN, NP, PA etc.).
- BSN with extensive field medical experience with a pharmaceutical company.
- Minimum of 5 years related work experience (clinical, managed care, or industry experience).
- Proficiency in GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use).
- Relevant therapeutic area knowledge, comprehensive understanding of product and safety profiles, and familiarity with managed care, health economics, reimbursement, and legal and regulatory landscape in the pharmaceutical/biotechnology industry.
Skills
- Deep scientific expertise in assigned molecules/products and therapeutic areas.
- Ability to build and leverage relationships with key external scientific and medical customers.
- Continuous learning within the therapeutic area, active participation in upskilling programs, and adherence to guidelines and procedures.
Benefits
- Discretionary annual bonus based on individual and Company performance.
- Details of benefits can be found at the provided link.
Pay
The expected salary range for this position is $161,000 - $299,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.
Schedule
This position requires significant use of a company-provided car to perform the essential duties and responsibilities of the role. Business travel, by air or car, is required for regular external business meetings with customers and intermittent internal company meetings (up to 70% of time).