Manager / Associate Director, Medical Information

Insmed   •  

Bridgewater, NJ

5 - 7 years

Posted 243 days ago

This job is no longer available.

Job Description


The Medical Information Manager/Associate Director will be responsible for creating/updating/reviewing the standard and customized letters/ FAQs of response related to Insmed products as well as communicating the information to internal and external stakeholders.


  • Creates, updates, and reviews standard and customized response letters and FAQs containing information available from reliable sources, including published medical literature, recently concluded clinical trials and data analyses, changes in product labeling, and from recent changes in regulations
  • Ensures that responses to unsolicited medical inquiries and requests for medical information from healthcare professionals are in keeping with Insmed’s Medical Information Standard Operating Procedures and in-line with Regulatory Authority regulations
  • Conducts advanced literature searches for education and incorporation into medical information letters
  • Summarize literature, clinical protocols, and clinical study reports
  • ·Responds to medical inquiries from healthcare professionals from Insmed’s Corporate website, Medical Science Liaisons, as well as other sources
  • Train front-line Medical Information Call Center on disease state and product information
  • Collaborate continuously with Medical Information Call Center
  • Assist staff the medical information booths at conferences to provide unsolicited medical information to healthcare providers
  • Ensure that all information pertaining to adverse events or product complaints received by Medical Information staff are forwarded to Insmed’s Pharmacovigilance and/or Quality Assurance Department, respectively


  • Requires an advanced degree (e.g. PharmD, MD, PhD) and a minimum of 5 years working in a Medical Information capacity at a pharmaceutical or biotech company, ideally in the area of Pulmonology and/or Infectious Diseases
  • Thorough understanding of regulations, compliance and industry standards relating to communicating product information to HCPs and/or consumers
  • Must be a team player, assertive communicator, and willingness to continuously learn the disease state, product, etc.
  • Proficiency in medical writing, able to correctly understand, correctly interpret, and accurately communicate scientific data and statistical analyses
  • Excellent communication (written, verbal, presentation) and analytical skills in a dynamic environment
  • Proven competency in utilizing literature search engines (EMBASE, PubMed, etc.)
  • Demonstrates a strong command of the English language (oral and written)
  • Proven ability to effectively work and thrive in a multi-cultural and cross-functional environment, while building strong relationships with all levels of people and teams
  • Proven ability to work within a multi-functional team (legal, regulatory, clinical/medical, quality, research, etc.)