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Medical Content Development Specialist

Eversana
EVERSANA
2+ years
Not Disclosed
10 Jan. 9, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Medical Content Development Specialist – Remote (Dublin, Ireland)

Company: EVERSANA
Location: Dublin, Ireland (Remote, home office based – EU/UK work eligibility required)
Job Type: Full-Time
Department: Clinical & Medical
Job Family: Medical Writing
Experience Required: 2+ years in Medical Information, Medical Writing, or Pharmaceutical Industry


Position Overview

EVERSANA is seeking a Medical Content Development Specialist to create and manage high-quality scientific and medical content for clients in the pharmaceutical, biopharmaceutical, medical device, and digital therapeutics sectors. This role is home-based, supporting global Medical Information (MI) and Medical Affairs (MA) engagements, including integrated commercialization partnerships.

The ideal candidate has experience in medical content development, medical writing, or medical communications, with strong scientific knowledge, project management skills, and excellent verbal and written communication abilities.


Key Responsibilities

Medical Content Development

  • Create and develop medical and scientific materials, including:

    • Scientific Response Documents (SRDs)

    • Frequently Asked Questions (FAQs)

    • Slide decks, abstracts, and posters

    • Educational and training materials

  • Support the full lifecycle of content development, from material gathering to Medical/Legal/Regulatory (MLR) review facilitation

  • Perform fact-checking and ensure scientific accuracy of medical documents

  • Use document management platforms (e.g., Veeva PromoMats / MedComms) for uploading, referencing, and annotations

Client Engagement & Support

  • Participate in client meetings and contribute to strategic discussions for content development projects

  • Support thought leadership initiatives, including publications, blogs, newsletters, and congress presentations

  • Mentor and coach team members; support hiring and onboarding activities

Operational Excellence

  • Maintain knowledge of industry best practices and regulatory standards for Medical Information and Medical Affairs materials

  • Collaborate with internal teams to implement new technologies and improve efficiency and quality of content

  • Ensure timely delivery of high-quality, compliant, and client-aligned content

Project Management & Compliance

  • Manage multiple projects simultaneously, meeting deadlines and maintaining scientific rigor

  • Ensure compliance with industry standards, codes of practice, and client requirements

  • Proactively flag and manage quality issues, implementing corrective actions when needed

Travel & Work Schedule

  • Flexible full-time hours, may include up to 10–15% business travel

  • Home-based role with EU/UK work eligibility required


Required Qualifications

Education:

  • Master’s or Doctorate in Life Sciences, Healthcare, or equivalent (Pharm.D., MPharm, MD, or PhD preferred)

Experience & Skills:

  • 2+ years in pharmaceutical industry, Medical Information, Medical Writing, or Medical Communications

  • Experience developing global medical content (SRDs, FAQs, CRDs, slide decks, etc.)

  • Excellent written and verbal communication skills in English; fluency in additional European languages (B2/C1/C2) is a plus

  • Proficient in Microsoft Office, Acrobat, and reference management software (EndNote, Mendeley, Citavi)

  • Strong literature search skills (PubMed, Ovid, Embase, etc.)

  • Knowledge of regulatory requirements and best practices for medical content

Professional Traits:

  • Analytical and critical thinking skills to interpret complex scientific data

  • Results-driven and project management capability

  • High ethical standards, professionalism, and integrity

  • Collaborative mindset with ability to mentor and coach junior team members

  • Innovative, able to transform ideas into practical solutions


Why Join EVERSANA

  • Remote work flexibility in Ireland and EU/UK

  • Opportunity to develop high-impact medical content across multiple therapeutic areas

  • Work with a global, inclusive, and innovative healthcare organization

  • Engage in projects that support patient care, HCP education, and evidence-based medicine


Diversity & Inclusion

EVERSANA is an Equal Opportunity Employer committed to diversity, equity, and inclusion. Reasonable accommodations are provided in accordance with applicable laws, including the ADA.


Apply Now

Join EVERSANA as a Medical Content Development Specialist to contribute to global medical communications, support innovative therapies, and make a meaningful impact on patient care.