Company: EVERSANA
Location: Remote (Global)
Job Type: Full-time
Department: Clinical & Medical
Job Family: Medical & Regulatory Affairs
About EVERSANA
EVERSANA is a globally recognized leader in next-generation commercialization services for the life sciences industry. Certified as a Great Place to Work, we are committed to creating a healthier world by supporting over 650 clients, from innovative biotech startups to established pharmaceutical companies. With a team of 7,000+ employees, we provide end-to-end solutions that help bring life-changing therapies to market while improving patient outcomes.
At EVERSANA, we embrace diversity, equity, and inclusion, fostering a culture where every employee can thrive. Our core values—Patient Minded, Client Delight, Take Action, Grow Talent, Win Together, Communication Matters, Embrace Diversity, and Always Innovate—drive our mission to revolutionize healthcare.
Job Description
Key Responsibilities:
- Conduct scientific data fact-checking and review promotional & non-promotional materials for Medical, Legal, and Regulatory (MLR) compliance.
- Ensure scientific accuracy, contextual correctness, and fair data presentation in alignment with industry regulations.
- Review and proofread medical content, verifying claims against clinical references.
- Collaborate with medical signatories, MLR teams, and clients to resolve findings efficiently.
- Utilize Veeva PromoMats/MedComms and other document management platforms.
- Support Medical Affairs, Medical Information, and Medical Communications by developing Scientific Response Documents (SRDs), FAQs, slide decks, and training materials.
- Contribute to SOPs, checklists, and style guides to enhance content quality.
- Work cross-functionally with medical writers, reviewers, and creative teams to ensure compliance and accuracy.
Qualifications & Skills:
- PharmD, PhD, MBBS, BDS, MDS, or M.Pharm/MS Pharm with 2+ years in scientific writing/review.
- Experience in literature searches (PubMed, Ovid, Embase, RightFind) and medical terminology.
- Strong understanding of regulatory requirements (FDA, EMA, etc.) for promotional/non-promotional content.
- Proficiency in Microsoft Office, Adobe Acrobat, and Veeva Vault.
- Excellent communication, project management, and analytical skills.
- Ability to work in fast-paced, cross-functional teams across multiple therapeutic areas (oncology, rare diseases, immunology, etc.).
Why Join EVERSANA?
✅ Remote Work Flexibility – Work from anywhere while contributing to global healthcare innovation.
✅ Impactful Work – Help bring life-saving therapies to patients worldwide.
✅ Career Growth – Access to continuous learning and leadership development.
✅ Inclusive Culture – A diverse, supportive, and collaborative work environment.
