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Senior Medical Content Strategist
3 weeks ago
The ideal candidate should have a strong foundation in medical and scientific writing, particularly in medico-marketing/marketing communications.
They must possess experience as a people manager, overseeing a team of 4+ medical content writers for both US & global markets.
A deep understanding of the pharmaceutical, life-sciences, medical devices, and healthcare industry is essential, along with the ability to grasp complex information and create clear and engaging content.
Key Responsibilities:- Content Development: Analyze project briefs, guide content writers and cross-functional teams on scope of work. Conduct research, write, and edit a wide range of medical communication materials, including scientific manuscripts, medical marketing collateral, and educational content.
- Create content outlines, storylines, and adapt content to align business objectives, campaign plans, and communication goals. Review and proof-read content for quality and accuracy.
- Develop various types of collaterals, including print materials (brochures, POS material, posters, newsletters, patient cards), digital materials (emails, iDetails, E-learning modules, social media posts, slides, PPTs), and audio-visual materials (educational videos, MoA Videos, 2d/3d animations).
- Scientific Accuracy: Ensure the accuracy, integrity, and scientific rigor of all content by staying up-to-date with the latest developments in healthcare, pharmaceuticals, and relevant therapeutic areas.
- Audience Adaptation: Write/adapt/customize content to diverse target audiences, including healthcare professionals, patients, and regulatory authorities, while maintaining scientific integrity and regulatory compliance.
- Collaboration: Collaborate with cross-functional teams, including medical experts, graphic designers, digital coding experts, project managers, clients, and client servicing teams, to produce cohesive and effective communication materials.
- Regulatory Compliance: Comply with industry guidelines, regulatory requirements, and ethical standards to ensure all content meets the highest standards of quality and compliance.
- People & Project Management: Manage multiple projects simultaneously, ensuring timely completion and adherence to scope. Work closely with peers and colleagues from the content writing team, review content created by fellow team members, train, mentor, and guide new team members on content writing and best practices.
- Ensure optimal utilization of all team members, prepare and submit reports about team members, including quality, timeliness, utilization, and other key performance indicators.
- Feedback Integration: Incorporate feedback from clients and internal stakeholders to continually improve and refine content.
- Content Approval Support: Be aware of different types of submissions involved in content approval by clients/regulatory bodies/healthcare authorities, preferably in the US, UK, EU, Middle East, and Asian markets. Hands-on experience with Veeva Vault PromoMats is essential, and other submission processes are an added advantage.
- Master's degree in a relevant field (e.g., life sciences, pharmacy) is required. Advanced degrees (e.g., PhD) are highly valued.
- Minimum of 5+ years of experience in medical communications, medical writing, or a related field and 2+ years as people manager/team lead.
- Strong understanding of the pharmaceutical and healthcare industry, including knowledge of clinical trials, drug development, regulatory processes, and marketing activities.
- Exceptional writing and editing skills, with the ability to convey complex scientific concepts in a clear and engaging manner.
- Proficiency with industry-specific software and tools (e.g., Microsoft Office, EndNote, reference management software, Veeva Vault, Aprimo).
- Strong attention to detail and ability to work independently or as part of a team.
- Knowledge of industry guidelines, including ICH-GCP, PhRMA, and CONSORT, is highly desirable.
- Flexibility to work in different time zones (preferably US and European timezones).
