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Medical Content Development Manager

0-2 years
Not Disclosed
10 April 29, 2025
Job Description
Job Type: Full Time Remote Education: Master’s degree in Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:
Medical Content Development Manager

Company:
EVERSANA

Location:
Remote (Eligible in UK, Ireland, Spain, Italy, Poland, Germany, or Portugal – must be legally authorized to work in the EU/UK)

Function:
Clinical & Medical – Medical Writing

Work Pattern:
Full-time


Job Description:
The Medical Content Development Manager is a key role within EVERSANA’s Global Medical Information/Medical Content Development Team. This role supports the development and management of scientifically rigorous, evidence-based, non-promotional medical content, including response documents, FAQs, slide decks, and training materials. The position involves strategic content development, document management, and cross-functional collaboration to support clients’ medical affairs and information needs globally.


Key Responsibilities:

  • Lead creation and management of medical/scientific content (e.g., SRDs, FAQs, slide sets, posters, abstracts).

  • Drive end-to-end content development and MLR (medical/legal/regulatory) review processes.

  • Use platforms like Veeva PromoMats/MedComms for document management and annotation.

  • Perform fact-checking and literature searches using tools like PubMed, Embase, and EndNote.

  • Collaborate with medical writers, creative teams, and clients to ensure quality deliverables.

  • Attend client meetings and contribute to content strategy and execution.

  • Support updates to SOPs, templates, style guides, and process documentation.

  • Remain current with industry best practices and regulatory standards.

  • Potential travel of 10–15%.


Qualifications:

  • Education:

    • Minimum: Master’s degree in Life Sciences, healthcare, or equivalent.

    • Preferred: Pharm.D., Ph.D., M.D., or relevant clinical/life science degree.

  • Experience:

    • Minimum 2 years in pharma or medical content development (medical writing, MI/MedComms).

    • Experience developing global medical information materials (SRDs, CRDs, FAQs).

    • Familiarity with compliance for promotional and non-promotional material review.

  • Skills:

    • Exceptional written, verbal, and presentation communication.

    • Proficiency in literature databases and citation tools (PubMed, EndNote, etc.).

    • Understanding of industry regulations and medical affairs functions.

    • Strong analytical thinking, critical reasoning, and project management.

    • Fluency in English (written and spoken); knowledge of additional EU languages (B2/C1/C2) is a plus.


Cultural & Role Expectations:

  • Demonstrate EVERSANA’s values: Patient Minded, Client Delight, Take Action, Embrace Diversity, Always Innovate, and Win Together.

  • Work independently while collaborating with global teams and clients.

  • Ensure content accuracy, compliance, and timeliness.

  • Handle multiple priorities in a matrix team setting.