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Medical Science Liaison - Metabolic

Job in Bridgewater, Plymouth County, Massachusetts, 02324, USA
Listing for: Recordati
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Medical Imaging
Salary/Wage Range or Industry Benchmark: 125000 - 150000 USD Yearly USD 125000.00 150000.00 YEAR
Job Description & How to Apply Below

This position is with Recordati Rare Diseases, Inc. (RRD), North America, an affiliate of Recordati.

Recordati Rare Diseases, Inc. (RRD) develops high-impact therapies for rare diseases, focusing on providing treatments to underserved communities in the U.S. Our mission is to mitigate the impact of rare diseases through increased awareness, better diagnoses, and improved treatment access in endocrinology, metabolic, hematology and oncology franchises. RRD is dedicated to fostering a dynamic work environment that promotes professional growth and a significant impact on patients' lives.

Reporting

Structure

Reports To:

Senior Director, Medical Affairs
Direct Reports:
None
Areas Managed:
Medical Affairs Initiatives

Overview

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 Acute Intermittent Porphyria (AIP), Cystinosis, Urea Cycle Disorders such as NAGS Deficiency, and Organic Acidemias (PA/MMA) 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.

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 Acute Intermittent Porphyria (AIP), Cystinosis, NAGS deficiency and Organic Acidemias understanding and product information for Panhematin, Cystadrops, Carbaglu.
  • 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.
  • 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., M.S.) or clinically relevant degree (RD, CGC, RN, PA) 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 critic 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 and communication skills.
  • Project management experience a plus.
  • Experience with rare diseases preferred (including Medical Affairs, clinical practice, research).
  • Excellent time management and ability to work independently.
  • Excellent English written and verbal communication skills.

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