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Medical Content And Review Specialist

2+ years
Not Disclosed
10 April 29, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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 and Review Specialist

Company:
EVERSANA

Location:
Remote – Preferred locations include Poland, Germany, Ireland, the UK, Italy, Portugal, or Spain. Applicants must be legally eligible to work in the EU or UK.

Function:
Clinical & Medical – Medical & Regulatory Affairs

Work Pattern:
Full-time


Job Description:
The Medical Content and Review Specialist plays a central role in ensuring healthcare promotional and non-promotional materials meet medical, legal, and regulatory (MLR) standards. This role manages end-to-end MLR processes, supports document reviews in systems like Veeva Vault PromoMats/MedComms, and facilitates compliant communication development. The specialist also supports project management within Medical Affairs, ensures SOP compliance, and contributes to accurate and timely client delivery.


Key Responsibilities:

MLR Process Management:

  • Coordinate the full MLR review cycle: scheduling, agendas, live meetings, and meeting minutes.

  • Maintain compliance using tools like Veeva Vault.

  • Ensure materials meet submission requirements and reject incomplete or incorrect ones.

  • Uphold and enforce evolving client policies and MLR SOPs.

  • Quality check final documents against approved versions.

Medical Content Support:

  • Assist with project planning and content development.

  • Upload and annotate materials in review platforms.

Project Management Support (Medical Affairs):

  • Support medical initiatives through structured project planning.

  • Collaborate with medical leadership to meet timelines and deliverables.


Qualifications:

  • Education:

    • Degree in Life Sciences, Biomedical Sciences, or related field required.

    • Postgraduate degrees in Pharmacy or Medicine preferred.

  • Experience:

    • Minimum 2 years in a healthcare agency or pharmaceutical company.

    • Hands-on experience with Veeva Vault PromoMats / MedComms.

    • Familiarity with MLR reviews, scientific writing, and meeting management.

  • Skills:

    • Strong communication (verbal and written) in English.

    • Proficiency in Microsoft Office Suite.

    • Attention to detail and ability to follow SOPs.

    • Excellent project and time management.

    • Familiarity with global healthcare compliance and advertising regulations (preferred).


Cultural Fit and Expectations:

  • Embody EVERSANA’s values like Client Delight, Patient Minded, Always Innovate, and Win Together.

  • Collaborate effectively across departments and maintain a solution-oriented mindset.

  • Work independently and manage multiple priorities in a remote setup.

  • Be proactive, dependable, and uphold high standards of ethics and quality.