Department: Clinical & Medical
Job Family: Medical & Regulatory Affairs
Employment Type: Full-time
Location: Remote (Work from Home)
Travel Requirement: Up to 10%
Work Hours: ~40+ hours/week
EVERSANA is a leading global provider of next-generation commercialization services to the life sciences industry. With over 7,000 employees worldwide and more than 650 clients—from biotech startups to global pharmaceutical leaders—our mission is to create a healthier world. Our services support drug development, regulatory, market access, medical information, and patient services, helping bring innovative therapies to market and improve patient outcomes.
We are committed to building a diverse and inclusive workplace, aligned with our Cultural Beliefs:
Patient Minded – Act with the patient’s best interest in mind
Client Delight – Own every client experience and its impact
Take Action – Be empowered and empower others to act now
Grow Talent – Own your development and support others
Win Together – Collaborate passionately for shared success
Communication Matters – Foster transparent, timely dialogue
Embrace Diversity – Promote awareness and respect
Always Innovate – Be bold and creative in everything
As a Medical and Scientific Reviewer, you will play a key role in EVERSANA’s Global Medical Content Development and Medical/Scientific Review Team. You will be responsible for fact-checking, reviewing, and ensuring scientific accuracy and compliance of promotional and non-promotional materials across a wide range of therapeutic areas.
This position requires strong medical/scientific expertise, attention to detail, regulatory knowledge, and the ability to interpret and communicate complex data effectively.
Perform scientific fact-checking and review of promotional and non-promotional materials for MLR (Medical, Legal, Regulatory) review.
Verify accuracy, completeness, and contextual appropriateness of all claims and content.
Ensure:
Data is scientifically balanced, clinically relevant, and statistically valid
References are acceptable and adequately support claims
Consistency with approved label and medical strategy
Collaborate with internal teams and client medical signatories to ensure alignment and compliance.
Support creation of materials such as:
Scientific Response Documents (SRDs)
FAQs, slide decks, posters, abstracts, and training materials
Review and annotate documents using tools like Veeva PromoMats / MedComms
Provide input to SOPs, templates, checklists, and style guides
Participate in client meetings and collaborate on strategic communication approaches
Ensure timely resolution of issues impacting review timelines
Recommend improvements to reduce recurring content or process issues
Maintain compliance with industry standards and regulatory requirements
Proactively address quality issues and ensure corrective actions
One of the following degrees:
PharmD, PhD, M.Pharm, MS Pharm, MBBS, BDS, MDS
2+ years of experience in scientific writing or quality control in the pharmaceutical/life sciences industry
Experience in:
Scientific literature searches and analysis (PubMed, Embase, RightFind, Ovid, etc.)
Document review and referencing in Veeva Vault or similar platforms
Clinical trials, medical terminology, and the drug development lifecycle
Working across multiple therapeutic areas (e.g., oncology, rare diseases, immunology)
Strong medical/scientific acumen
Excellent written and verbal communication
Detail-oriented with excellent time management
Proficiency in Microsoft Office, Adobe Acrobat, and other documentation tools
Ability to work independently and cross-functionally
Deep understanding of regulatory requirements for Medical Affairs, Medical Information, and promotional material review
Experience with medical content development and reference validation
Strong project management and stakeholder collaboration experience
Ability to thrive in a fast-paced, matrix environment
High level of professional integrity and ethical conduct
Agile learner with the ability to work across multiple disease areas
Remote-first flexibility
Inclusive and collaborative team culture
Opportunities for growth and continuous learning
Supportive of diversity, equity, and inclusion
Commitment to client delight and patient-centered outcomes
EVERSANA is aware of fraudulent job offers misusing its name. We never request payment or personal information during the hiring process.
EVERSANA is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, gender, disability, veteran status, religion, or other protected characteristics.
Visit EVERSANA Careers to submit your application or follow us on LinkedIn or Twitter for updates.
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