Medical Affairs Manager

Medical Affairs Manager – Digital Health
6 month contract
Remote, EST hours

Requirements

Oversee and support digital health and digital medicine initiatives aligned with Medical Affairs objectives.
Provide medical, scientific, and technical support for assigned products and digital health programs.
Serve as a medical subject matter expert to support product development activities.
Participate as a Medical Affairs representative on cross-functional product and brand teams.
Collaborate with matrix partners to review and provide input on clinical development and regulatory documentation.
Provide medical support for company-sponsored and investigator-initiated research activities.
Ensure Medical Affairs activities are aligned with development and commercial objectives, including publication and congress strategies.
Coordinate the development, review, and dissemination of scientific materials, including abstracts, posters, presentations, symposia, and manuscripts.
Support interactions with healthcare professionals to gather feedback on strategy, publications, and scientific initiatives.
Assist with the planning and execution of medical and scientific advisory boards, including coordination of healthcare professional engagement activities.
Review and contribute to internal and external medical and promotional materials to ensure scientific accuracy and appropriate communication of data.
Participate in cross-functional and interdepartmental projects as needed.

Qualifications

Minimum of a Master’s degree, PhD, MD, PharmD, PMHNP, or PsyD.
4–7 years of experience within Pharmaceutical Industry Medical Affairs.
Candidates with a strong scientific background in Digital Health, Digital Therapeutics, or startup environments may also be considered.
Experience in Digital Health, Digital Therapeutics, and/or Neuroscience required; Psychiatry experience preferred.
Product launch experience is preferred.
Demonstrated ability to manage multiple projects simultaneously in a fast-paced environment.
Strong communication, presentation, and interpersonal skills, including experience presenting to large audiences.
Experience developing and managing budgets.
Working knowledge of OPDP promotional regulations and pharmaceutical promotion standards.
Working knowledge of CDER and CBER regulations related to the evaluation and approval of pharmaceutical products.
Proficiency with Microsoft Office applications.
Self-motivated, solutions-oriented, and capable of working effectively in cross-functional environments.