Medical Science Liaison, Endocrinology (NYC)

Recordati•Bridgewater, NJ

13d•$160,000 - $220,000•Onsite

About The Position

Recordati Rare Diseases, Inc. (RRD), North America, an affiliate of Recordati, is seeking a field-based Medical Science Liaison (MSL) in endocrinology. RRD develops therapies for rare diseases and works to increase awareness, improve diagnoses, and enhance treatment availability in endocrinology, metabolic, and oncology areas. The MSL will foster collaborative relationships with opinion leaders focused on Cushing’s Syndrome, Cushing’s Disease, and Acromegaly, and facilitate the exchange of unbiased scientific information between the medical community and the company. The role serves as a clinical and medical affairs peer-to-peer liaison internally and externally, and reports to the Director, Medical Affairs or designee. There are no direct reports; the position manages Medical Affairs initiatives. The position is field-based near a major airport and requires approximately 60% travel. It operates in a professional office environment and routinely uses standard office equipment. Travel may include out-of-state meetings over weekends and at night. The employee must be able to travel by car, train, and plane, hold a valid driver’s license, and have transportation. The role is largely sedentary, with frequent standing, walking, use of hands, reaching, talking, and hearing; occasional lifting or moving of up to 25 pounds is required. The employee must be able to fly on commercial airlines. The expected salary range is $160,000–$220,000, depending on skills, competency, and market demand. Compensation also includes an annual bonus and benefits. The position is classified as exempt.

Requirements

Advanced scientific degree (M.D., D.O., Ph.D., or Pharm.D.) in medical or biological sciences.
Familiarity with the drug development process and FDA, ICH, and GCP guidelines.
Ability to review and interpret clinical data.
Ability to develop clinical data and medical content for internal and external presentations.
Proficiency with Microsoft Office, including Word, PowerPoint, and Excel.
Strong presentation skills.
Excellent time management and ability to work independently.
Excellent written and verbal communication skills.
Valid driver’s license and means of transportation.
Ability to travel by car, train, and plane, including commercial air travel; approximately 60% travel is required.
Ability to meet the physical demands of the role, including occasional lifting or moving of up to 25 pounds.

Nice To Haves

At least two years of experience in Medical Affairs or clinical functions is strongly preferred.
Experience implementing, monitoring, or managing clinical trials in academic clinical research or at a pharmaceutical or biotechnology company.
Project management experience.
Experience with rare diseases, including in Medical Affairs, clinical practice, or research.

Responsibilities

Deliver clinical and scientific presentations to healthcare professionals, including clinicians and P&T committee members, and provide current medical, disease, and product information.
Provide scientific support at medical conferences, including information on Cushing’s Syndrome, Cushing’s Disease, Acromegaly, 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 publications, investigator-initiated trials, and company-sponsored research.
Support clinical initiatives, including assessing and selecting clinical investigations, identifying sites, supporting registries, and presenting 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 the sales team, on relevant scientific and medical topics.
Participate in developing and reviewing professional slide decks, medical letters, and clinical summaries.
Develop a territory plan with input from the direct line manager.
Gather clinical field insights and regularly inform the team through appropriate channels.
Understand the role and contributions of Medical Science Liaisons and Medical Affairs.
Comply with applicable laws, regulations, and policies, including adverse-event and pharmacovigilance responsibilities.
Perform additional duties as assigned.