Develop and review all relevant medical affairs content
Independent writing and development of drafts including researching, organizing, compiling, interpreting and quality check of various types of technical and/or medical information with limited support from internal reviewers
Review of drafts including checking content pieces developed by other team members for clarity, perspective, accuracy, appropriateness for target audience, and overall quality
Train other team members in processes, and overall writing to ensure adherence to quality standards
Serve as a functional expert for the product and support junior team members to enhance familiarity with product specific communication requirements
Provide solutions to authors for projects and collaborate with other teams to drive these solutions
Maintain open & independent communication with authors and stakeholders within the MCC team
Ensure delivery of all projects within expected timelines while adhering to all quality and compliance requirements for medical content
Identify and train to become an expert on one new tool/skill for content creation representing the latest trends in the industry

Advanced scientific degree (eg, MRes, MPharm, MSc, PhD, PharmD, MBBS/MD, MSc, MPH, MPharm)
5+ years of experience in writing/developing medical content for the pharmaceutical industry, academic settings, CRO, or biotech company
Ability to lead and execute a project end-to-end
Strong interpersonal skills to quickly build rapport and credibility with team members, authors and key external stakeholders cross culturally/regionally to drive solutions ahead
Effective English verbal and written communication with flexibility to be clear, consistent, compliant, and appropriate for a variety of settings
Demonstrated ability to lead projects independently and engage diverse stakeholders
Understand the applications of technology to medical content development.

Program Manager, Medical Communications and Content Solutions – Vaccines

Key skills