Harrow is hiring a
Manager of Medical Affairs in Worldwide

Summary

The Medical Affairs Manager at Harrow is responsible for executing medical affairs strategies, supporting publication planning, establishing professional relationships with the medical community, partnering with other departments, fostering an environment of compliance, and having a terminal degree and ophthalmology experience. The position is remote and requires up to 30% travel.

Requirements

• Terminal Degree required. MD/DO/OD/PhD/PharmD
• Ophthalmology experience required. Dry Eye Disease experience preferred
• Minimum of 4 years of pharmaceutical industry experience in a Medical Affairs capacity required
• Working knowledge of the Healthcare System and of the research procedures as well as the ICH guidelines, GCP, and other ethical guidelines
• Proven ability and experience to develop and foster peer-to-peer, credible relationships with Medical Experts/decision makers
• Strong analytical skills, ability to interpret scientific/clinical literature
• Proficient with MS Office applications
• The ability to fluently read, write, understand, and communicate in English required

Responsibilities

• Execute Medical Affairs strategies including engagement with opinion leaders, investigator-led research, HEOR, and data dissemination
• Support publication planning, medical writing, medical advisory boards, educational programs, conferences, and responding to requests for medical information
• Establish professional relationships with the medical community and exchange scientific knowledge with global and regional key opinion leaders
• Partner with other departments to ensure timely, accurate, and compliant preparation and review of promotional and educational material
• Execute a strategic publication and congress plan; work with internal colleagues to develop key messages on unmet need, mechanism of action, target product profile, and among others
• Partner with Clinical Operations and Clinical Development to facilitate enrollment of company sponsored clinical trials
• Work collaboratively with cross-functional colleagues (e.g. marketing, sales, patient advocacy, clinical, regulatory, legal and market access) to develop and execute strategic plans

Benefits

Remote. Travel: Up to 30%