MSL, Medical Science Liaison

Job Area: R&D/Medical

Job Category:
Professionals

Job Site:
Remote

Location:

San Mateo, CA, US

Dompé is an Italian bio-pharmaceutical company that focuses on innovation, where a long tradition in the field of personal wellness goes hand-in-hand with a commitment to research and development to meet unsatisfied therapeutic needs.

Established in 1940 in Milan, Dompé has an industrial and biotech research hub in L’Aquila, in addition to branches in Europe (Barcelona, Berlin, Paris and Tirana). The company has approximately 900 employees. The US headquarters of Dompé are based in Boston (R&D) and in the San Francisco Bay Area (Commercial Operations).

The Medical Science Liaison (MSL) serves as a scientific and clinical expert within the ophthalmology therapeutic area, responsible for engaging external experts through fair-balanced, evidence-based scientific exchange. This role ensures compliance with PhRMA Code, internal policies, and all applicable regulations while supporting the generation and communication of scientific insights that inform Medical Affairs strategy. The MSL contributes to pre-launch readiness and pipeline support by building disease state expertise, facilitating clinical trial awareness, and preparing for future product introductions.

Through congress participation, insight collection, and collaborative teamwork, the MSL advances scientific understanding and strengthens relationships that ultimately support patient care and evidence-based decision-making.

• Responsible for conducting fair-balanced, evidence-based scientific exchange with ophthalmologists, optometrists and health care professionals.
• Responsible for identifying, profiling, and engaging appropriate external experts based on clinical expertise and scientific relevance.
• Responsible for delivering and discussing approved scientific materials, clinical data, and disease state information in accordance with PhRMA Code and internal policies.
• Responsible for appropriately handling unsolicited off-label questions through approved medical information processes.
• Responsible for accurately and timely entries of interactions and data into compliantly managed CRM systems.

• Responsible for systematically collecting, synthesizing, and reporting ophthalmic clinical and scientific insights from external experts.
• Responsible for ensuring insights are documented accurately and shared through approved systems to inform Medical Affairs strategy.

• Responsible for attending and supporting pre-, during-, and post-congress activities, including scientific exchange, booth coverage, and congress debriefs.
• Responsible for summarizing emerging data and competitive intelligence for internal stakeholders in a compliant manner.

• Responsible for developing disease state expertise and readiness for upcoming product launches.
• Responsible for engaging external experts on pipeline data and evolving treatment paradigms in a compliant, non-promotional manner.
• Responsible for supporting evidence generation activities and clinical trial awareness.

• Responsible for exemplifying a culture of scientific integrity, compliance, and collaboration across the field medical team and organization.
• Reponsible for mentoring peers, sharing best practices, and contributing to training materials.

All activities must be conducted in accordance with PhRMA Code, internal SOPs, and applicable laws and regulations. Scientific exchange must remain non-promotional and fair-balanced at all times.

• Advanced scientific degree (PharmD, PhD, MD, OD, or equivalent) required.
• Minimum 2–3 years of…