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Medical Information Specialist

1 month ago


Jersey City, New Jersey, United States BESTMSLs Full time
Job Summary

We are seeking a highly skilled Medical Information Manager to join our team at BESTMSLs. This is a hybrid role with three days/week in the Bridgewater, NJ office.

Key Responsibilities
  • Serve as the primary Medical reviewer for promotional materials and generate standard and customized medical information content to fulfill unsolicited Medical Information requests from healthcare professionals and non-healthcare professionals.
  • Develop and execute the content generation plan for the assigned therapeutic area, including preparation of a content generation plan to support a product launch.
  • Manage internal and external resources for the execution of the content generation plan.
  • Provide timely, accurate, thorough, and scientifically-balanced responses to escalations from the Medical Information Contact Center.
  • Provide on-going support and training to MICC agents and other relevant individuals on new or updated Medical Information content.
  • Regularly monitor the quality and accuracy of the Medical Information responses and identify necessary corrective actions or training required to ensure compliance with regional and local regulations as well as internally relevant SOPs.
Requirements
  • An advanced degree in pharmacy, nursing, or medicine (PharmD, NP, DNP, MD, PA) from accredited US or foreign medical school is required.
  • A minimum of 3 to 5 years of experience in Medical Information or Medical Communications with a pharmaceutical company/vendor, including medical review of promotional materials.
  • Product launch experience is preferred.
  • Completion of a pharmaceutical industry fellowship or a drug information residency is preferred.
  • Experience with rare diseases is preferred.
  • Knowledge of applicable regulatory and legal requirements for the provision of medical information in the pharmaceutical environment.
  • Knowledge of relevant FDA, EU, and ICH guidelines, initiatives, and regulations governing medical information in post-marketing products.
  • Demonstrated ability to work in a matrix environment.
  • Demonstrated ability to produce clear, concise, and effective written and verbal communications describing scientific and clinical data in English.
  • Demonstrated advanced medical information skills (e.g., literature searching, literature evaluation, data analysis, statistics).
Preferred Qualifications
  • Ability to build an excellent partnership with an outsourced partner, maintaining strong relationships while simultaneously holding the outsourced partner to high standards.
  • Ability to work independently with minimal supervision, multi-task, and work effectively under pressure; adapt to change as needed; possess excellent project management skills; attentive to details.
  • Ability to work collaboratively and coordinate the efforts of team members to resolve comments and produce a final high-quality document.
  • Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with team members.
  • Excellent computer skills. Strong proficiency in Microsoft programs: Excel, Word, PowerPoint, as well as Veeva systems.
  • Fluent in English (oral and writing).
Location/Travel

The location for this position is based at the HQ office in Bridgewater, New Jersey. This position may require occasional domestic and international travel (less than 10%).