EVERSANA is more than a service provider—it’s a driving force in creating a healthier world. Certified as a Great Place to Work across the globe, the company boasts a team of over 7,000 employees dedicated to next-generation commercialization services for the life sciences industry. Serving more than 650 clients, from innovative biotech startups to established pharmaceutical giants, EVERSANA helps bring therapies to market and supports patients who rely on them.
Grounded in core cultural beliefs like “Patient Minded,” “Client Delight,” and “Embrace Diversity,” EVERSANA fosters an inclusive culture that values unique backgrounds and experiences. The company is deliberate about building teams that prioritize integrity, innovation, and collaboration. As an Equal Opportunity Employer, EVERSANA champions Diversity, Equity & Inclusion (DEI), ensuring employees from all walks of life contribute to advancing healthcare. With a focus on areas like oncology, neurology, immuno-oncology, and immunology, EVERSANA’s integrated compliance team plays a pivotal role in helping biopharma companies innovate novel therapies for rare and critical diseases.
Joining EVERSANA means being part of a passionate community that “wins together” and “always innovates.” For professionals in pharma careers and medical writing jobs, it’s an ideal place to grow talent while making a tangible impact.
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Job Description: Expert Writer, Medical Content Development
This full-time, remote position falls under the Clinical & Medical department and Medical Writing job family. Reporting to the Manager, Medical Content Development, you’ll join EVERSANA’s Compliance Business Unit, collaborating closely with teams in Medical Information, Medical Affairs, Pharmacovigilance, Regulatory, and Quality. The role supports a diverse client base, including pharmaceutical, biotechnology, medical device, digital therapeutics, and over-the-counter companies—especially small and emerging ones.
As an Expert Writer in Medical Content Development, you’ll drive content-related engagements for integrated commercialization deals and standalone consulting services. Expect to work 40+ hours per week, with up to 10% travel (post-COVID), in a matrix team setting that values independence, ethical compliance, and strategic alignment.
Essential Duties and Responsibilities
- Support the Manager on medical content development for projects like Scientific Response Documents (SRDs), Frequently Asked Questions (FAQs), slide sets, abstracts, posters, education/training materials, and more.
- Lead the document development process: Gather materials, create scientifically accurate content, facilitate medical, legal, and regulatory (MLR) reviews, and manage discussions.
- Utilize platforms like Veeva PromoMats or MedComms as a content owner—uploading documents, anchoring references, and adding annotations.
- Perform scientific data fact-checking to aid MLR teams.
- Collaborate on strategy, tactical execution, and communication for assigned projects; participate in client meetings.
- Contribute to thought leadership (articles, newsletters, congress presentations, blogs) on medical content services.
- Help update SOPs, checklists, templates, style guides, and guidance documents.
- Mentor/coach team members, support hiring/onboarding, and evaluate new technologies for efficiency.
- Work cross-functionally with other medical writers and creative teams.
- All other duties as assigned, with reasonable accommodations for disabilities.
Expectations of the Job
- Deliver client delight through high-quality, compliant outputs.
- Oversee direct reports/consultants, ensure industry standards compliance (e.g., AMA Style, ICMJE, GPP, PRISMA).
- Work independently on ethical, strategically aligned medical writing while flagging quality issues.
- Collaborate with EVERSANA teams and take feedback from management/clients.
- Stay agile in learning multiple therapeutic areas.
This remote pharma job is perfect for those passionate about medical communications and improving patient outcomes.
Qualifications: Who We’re Looking For Minimum Knowledge, Skills, and Abilities
- PharmD (or M.Pharm./M.S. Pharm), PhD, or MD with proven medical writing and content development experience.
- 4+ years in life sciences/pharma, with direct experience in Medical Information, Medical Communications, or Scientific Communications.
- Exceptional written, oral, interpersonal, and presentation skills; ability to interpret complex data.
- Thrive in matrix teams, meeting timelines while interfacing with all levels.
- Familiarity with AMA Style, clinical research, statistics, and guidelines like ICMJE, GPP, PRISMA, STROBE, CONSORT.
- Proficient in Microsoft Office, Acrobat; experience with literature searches (PubMed, Ovid, Embase) and reference tools (EndNote, Mendeley).
- Strong grasp of regulatory best practices for Medical Affairs and promotional/non-promotional materials.
- Excellent project management; results-driven with integrity and collaboration skills.
- Agile learner across disease states/therapeutic areas.
Preferred Qualifications
- Experience in medical content for new product launches, especially Medical Information materials.
- Publishing background (abstracts, posters, manuscripts).
- Multi-therapeutic area expertise.
- Veeva Vault MedComms/PromoMats proficiency.