Sr. Manager / Associate Director, Publications and Medical Information

Sr. Manager / Associate Director, Publications and Medical Information (Contract) Job Responsibilities: Publications Contribute to development of Publication Strategy and Publication Plan (in coordination with the Publications Working Team) Execute publication tactics and the Publication Plan Manage the drafting process for clinical publications (with vendor/agency), tracking timelines and ensuring timely reviews, approvals, and submissions Interact with internal and external authors/KOLs related to clinical publications Manage record keeping and digital storage for publications-related materials, including publications metrics Data Reviews Contribute to development of data review slide decks and derivative materials (with vendor/agency) Support data presentation-related AI projects Congress Support Support booth staffing, congress materials, and presentation logistics (in coordination with Medical Affairs Operations) Provide dedicated congress/booth Medical Information support Medical Information Draft Standard Response Letters and manage related Medical and Legal review Ensure timely responses to medical inquiries; coordinate with the Medical Information team at a partner company and track inquiry volumes Create FAQs and reference materials (in coordination with internal Subject Matter Experts) Support Medical Information-related AI projects Education: Doctoral degree in a medical, biological, or related discipline (PhD, PharmD, MD; MS with relevant experience considered) Experience: 3-4 years of experience (Sr. Manager) or 4-5 years of experience (Associate Director) in Medical Affairs, Medical Communications, Clinical Publications, or Medical Information Demonstrated experience managing scientific/clinical publications end-to-end Familiarity with publication management and MLR processes/procedures Experience with medical information operations and Standard Response Letter (SRL) development Skills: Strong working knowledge of GPP, ICMJE, and industry compliance requirements Excellent scientific writing, editing, and critical literature-review skills Excellent communication skills Project management and time management skills, with the ability to operate within multiple concurrent timelines Cross-functional collaboration skills, with the ability to align with internal teams of Subject Matter Experts representing different functions Fit withCulture and Values Strong team orientation; highly collaborative Solutions and results-oriented focus Hands-on approach; resourceful and open to diverse points of view #J-18808-Ljbffr Planet Pharma