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Medical And Scientific Reviewer

2+ years
Not Disclosed
10 April 29, 2025
Job Description
Job Type: Full Time Education: PharmD, M. Pharm., M.S. Pharm, Ph.D., BDS, MDS, or MBBS 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 and Scientific Reviewer

Company:
EVERSANA

Location:
Remote (Global team)

Function:
Medical & Scientific Review / Medical Affairs

Work Pattern:
Full-time, Remote


Job Description:
The Medical and Scientific Reviewer position at EVERSANA provides an exciting opportunity to contribute to the global life sciences industry by reviewing and ensuring the scientific accuracy of promotional and non-promotional materials. You will be part of a dynamic team that supports various therapeutic areas, with a focus on creating high-quality, compliant content across different platforms.


Key Accountabilities:

  • Perform scientific data fact-checking and review of materials submitted for medical, legal, and regulatory (MLR) review.

  • Ensure scientific accuracy, relevance, and completeness of data.

  • Advise on claims and ensure they are supported by data and align with the approved label.

  • Collaborate with internal teams and clients to resolve issues impacting timelines and quality.

  • Support content creation for Medical Affairs, including scientific response documents, FAQs, abstracts, and training materials.

  • Participate in the development and review of SOPs, templates, and style guides.

  • Collaborate with cross-functional teams to enhance the content creation and review process.


Qualifications:

  • PharmD, M. Pharm., M.S. Pharm, Ph.D., BDS, MDS, or MBBS with relevant experience in scientific writing/reviewing.

  • Minimum of 2 years of experience in document QC and/or scientific writing within the life sciences or pharmaceutical industry.

  • Expertise in scientific literature searches and analysis (e.g., PubMed, Ovid, Embase).

  • Strong scientific acumen and understanding of therapeutic areas such as oncology, hematology, immunology, etc.

  • Proficiency in Microsoft Office, Acrobat, and content management platforms (e.g., Veeva Vault PromoMats).

  • Ability to manage projects, meet deadlines, and communicate effectively with internal and client teams.


Additional Information:

  • Ability to work independently while ensuring compliance with industry standards.

  • Must be highly detail-oriented and possess excellent time management and project management skills.

  • Travel up to 10% may be required.

  • Strong collaboration and communication skills across multiple departments and clients.