Manager, Medical Information

Bausch Health•Bridgewater, NJ

86d•Onsite

About The Position

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact. The Medical Information Manager provides accurate, evidence-based medical information to healthcare professionals and internal stakeholders while ensuring compliance with FDA regulations and company policies. This role evaluates scientific literature, develops medical response documents, and maintains medical information resources across multiple therapeutic areas. The position collaborates with Medical Affairs, Regulatory, Pharmacovigilance, and field medical teams to support product launches, AMCP dossiers, and scientific communications. The ideal candidate combines strong scientific expertise, project management skills, and cross-functional collaboration to deliver high-quality medical information services.

Requirements

Bachelors degree required.
Excellent verbal, written, and interpersonal skills are required
Must be able to consistently perform work requiring a high level of attention to detail
Proficiency in Microsoft Excel, PowerPoint and Word and a strong working knowledge of databases

Nice To Haves

Advanced degree (such as PharmD,PhD, etc) in the sciences is preferred
Fellowship in Medical Information or minimum of 2 years of related experience in a Medical Information department within the pharmaceutical industry is preferred.
Excellent task management skills including planning, prioritization, objective setting, and meeting management are strongly preferred
Ability to provide high level professional support to the management team and to establish effective working relationships with a diverse range of stakeholders
Demonstrate critical thinking skills with ability to anticipate issues and impact on related areas of an event or project

Responsibilities

Manage the dissemination of medical information correspondence related to various therapeutic areas (gastrointestinal related, dermatology, etc) to external customers (healthcare professionals) and internal customers (medical science liaisons, regulatory, etc) and ensure that all activities are conducted within the pharmaceutical regulatory framework.
Oversight of performing literature searches and critically evaluates scientific data.
Prepare standard response documents, continuously evaluate and update standard response letter database.
Ensure projects are completed on schedule following established procedures and timelines.
Create and review medical summary of published literature resources into standard response letter
Interact and provide guidance to responses to the vendor call center, including providing general training
Work within all relevant and newly published FDA guidance relating to medical information
Leads and/or contributes to the MI planning for new product launches, line extensions, key data releases, as applicable.
Proactively provides logical recommendations and solutions for medical information activities
Provides Medical Information support at conference booths, and learn the processes of booth activities
Works cross-functionally with other Medical A team members, as necessary airs, Regulatory, Pharmacovigilance matrix
Understand and execute on AMCP Dossier requests while interacting with HEOR and field medical teams, as needed
Assist with ad-hoc Medical A oversight from manager airs projects- Plans and coordinates projects with minimal Business travel (approx.10%) may be required for support at Medical Affairs scientific congresses and/or internal meetings