Medical Science Liaison, Endocrinology, California
Recordati
Summary
The Medical Science Liaison (MSL) will serve as our field-based scientific expert whose mission is to foster collaborative relationships with opinion leaders focused on Cushing’s Syndrome, Cushing’s Disease and Acromegaly and to facilitate the exchange of unbiased scientific information between the medical community and the company. The MSL will have the clinical/medical affairs expertise to serve as a peer-to-peer liaison internally and externally.
Job description
Essential Duties And Responsibilities
- Deliver clinical and scientific presentations to health care professionals, including clinicians (i.e., Endocrinologists, etc.) and P&T committee members. Support medical community with up-to-date medical information, robust diseases expertise and product information
- Provide scientific support at medical conferences and support medical community with up-to-date medical information, robust Cushing’s Syndrome, Cushing’s Disease and Acromegaly understanding and product information for Isturisa, Signifor and Signifor LAR.
- Maintain peer-to-peer collaborations and relationships with key medical experts in relevant therapeutic areas.
- Respond to unsolicited medical information requests using a customized approach.
- Collaborate with physicians on medical affairs initiatives including providing assistance with publications and investigator initiated trials as well as company sponsored research.
- Support clinical initiatives including assessment and selection of clinical investigations, site identification, registry and presentation of final approved data.
- Provide medical and scientific input into the planning and execution of Advisory Boards. Work with physician experts to review speaker presentations and provide medical references when requested.
- Train staff, including sales team on key scientific and medical topics in relevant therapeutic areas.
- Participate in the development and review of professional slide decks, medical letters, and clinical summaries.
- Responsible for developing territory plan with input from direct line manager.
- Gathers clinical field insights and informs team on a regular basis through appropriate channels.
- Understand the role and contributions provided by Medical Science Liaisons and Medical Affairs.
- Act in full compliance with all laws, regulations, and policies including adverse events / pharmacovigilance responsibilities.
- Perform additional duties as may be assigned.
Education And Experience
- Advanced scientific degree (M.D., D.O., Ph.D., Pharm.D.) in Medical, Biological Sciences required.
- Minimum of two years of experience in Medical Affairs/Clinical functions strongly preferred.
- Familiarization with drug development process, FDA, ICH, and GCP guidelines.
- Experience implementing, monitoring, and/or managing clinical trials for academic clinical research or pharmaceutical/biotechnology company a plus.
Knowledge And Skills
- Ability to review and interpret clinical data.
- Ability to develop clinical data and medical content for presentation to internal and external audiences
- Proficient in Microsoft Office suite of products (e.g., Word, PowerPoint, Excel).
- Strong presentation skills.
- Project management experience a plus.
- Experience with rare diseases a plus (including Medical Affairs, clinical practice, research).
- Excellent time management and ability to work independently.
- Excellent written and verbal communication skills
Location/Travel
- This position is field-based, near a major airport.
- Approximately 60% of travel required.
Requirements
- Advanced scientific degree (M.D., D.O., Ph.D., Pharm.D.) in Medical, Biological Sciences required.
- Minimum of two years of experience in Medical Affairs/Clinical functions strongly preferred.
- Familiarization with drug development process, FDA, ICH, and GCP guidelines.
- Experience implementing, monitoring, and/or managing clinical trials for academic clinical research or pharmaceutical/biotechnology company a plus.
- Ability to review and interpret clinical data.
- Ability to develop clinical data and medical content for presentation to internal and external audiences
- Proficient in Microsoft Office suite of products (e.g., Word, PowerPoint, Excel).
- Strong presentation skills.
- Project management experience a plus.
- Experience with rare diseases a plus (including Medical Affairs, clinical practice, research).
- Excellent time management and ability to work independently.
- Excellent written and verbal communication skills
Benefits
- 401(k) Matching
- Medical, Dental & Vision
- Mental Health Benefits
- Paid Time Off
- Paid Holidays
- Winter Holiday Shutdown
- Life & AD&D Insurance
- Weekly Complimentary Lunch
- Annual Bonus
Company overview
Recordati is a global pharmaceutical group founded in 1926 in Correggio, Italy, by Giovanni Recordati. Listed on the Italian stock exchange since 1984, the company has grown into an international pharmaceutical leader with approximately 4,580 employees operating in around 150 countries. Recordati focuses on two main business areas: Specialty and Primary Care, and Rare Diseases. The Specialty and Primary Care division develops and markets innovative treatments in cardiovascular, urological, gastrointestinal, and central nervous system therapeutic areas, including well-known products like Zanidip®, Urorec®, and Livazo®. The Rare Diseases division, established in 2007 through the acquisition of Orphan Europe, specializes in treatments for rare metabolic, endocrinological, and oncological conditions, with products such as Carbaglu®, Signifor®, and Isturisa®. With two chemical plants and seven manufacturing sites worldwide, Recordati maintains a strong commitment to research and development, continuously investing in medical innovations to improve patient lives while maintaining a sustainable business model with a focus on ethical practices and environmental responsibility.