Medical and Scientific Reviewer – EVERSANA | Remote Job Opportunity in Pune, India
Company Name: EVERSANA
Job Location: Pune, Maharashtra, India
Work Mode: Remote / Work From Home Available
Job Type: Full-Time
Department: Clinical & Medical
Industry: Pharmaceutical, Biotechnology, Medical Affairs, Scientific Communications
About EVERSANA
EVERSANA is a globally recognized life sciences services organization dedicated to creating a healthier world through innovative healthcare commercialization solutions. With a workforce of 7,000+ professionals worldwide, EVERSANA partners with pharmaceutical, biotechnology, medical device, and healthcare companies to accelerate the delivery of life-changing therapies to patients globally.
The company supports more than 650 clients ranging from emerging biotech startups to leading multinational pharmaceutical organizations. EVERSANA is also recognized globally as a Great Place to Work and promotes a diverse, inclusive, and innovation-driven work culture.
Job Title: Medical and Scientific Reviewer
Job Overview
EVERSANA is hiring experienced Medical and Scientific Review professionals for its Global Medical Affairs and Medical Content Development team. This opportunity is ideal for candidates with expertise in scientific writing, medical review, promotional and non-promotional content review, medical communications, and regulatory compliance within the pharmaceutical and life sciences industry.
The selected candidate will work closely with Medical Affairs, Medical Information, Medical Communications, and MLR (Medical, Legal & Regulatory) review teams to ensure scientific accuracy, regulatory compliance, and high-quality medical content across multiple therapeutic areas.
This role demands strong scientific acumen, analytical thinking, attention to detail, and expertise in reviewing scientifically balanced pharmaceutical content.
Experience Required
Minimum 2+ years of experience in:
Scientific Writing
Medical Review
Document Quality Check (QC)
Medical Communications
Medical Information
Pharmaceutical Content Review
Freshers Eligibility
Freshers are generally not eligible for this role. Candidates must possess prior industry experience in medical/scientific review or related pharmaceutical documentation functions.
Educational Qualification
Candidates with the following educational backgrounds may apply:
PharmD
M.Pharm
MS Pharm
PhD
MBBS
BDS
MDS
Key Responsibilities
Medical & Scientific Review
Perform scientific fact-checking and detailed review of promotional and non-promotional pharmaceutical materials.
Ensure medical content is:
Scientifically accurate
Clinically relevant
Statistically appropriate
Contextually balanced
Regulatory compliant
MLR Review Support
Participate in Medical, Legal & Regulatory (MLR) review processes.
Review claims, references, scientific data, and supporting evidence.
Ensure all claims align with approved product labeling and applicable regulations.
Medical Communications
Support development and review of:
Scientific Response Documents (SRDs)
Frequently Asked Questions (FAQs)
Medical Slide Decks
Scientific Abstracts
Posters
Educational Materials
Training Content
Medical Affairs Documents
Scientific Literature Analysis
Conduct literature searches using:
PubMed
Ovid
Embase
RightFind
Analyze and summarize scientific publications and clinical data.
Cross-Functional Collaboration
Work with:
Medical Affairs Teams
Medical Writers
Regulatory Teams
Creative Teams
Client Stakeholders
Ensure timely review cycles and content approvals.
Document Management
Utilize platforms such as:
Veeva Vault PromoMats
Veeva MedComms
Upload documents and manage annotation/reference anchoring processes.
Required Skills
Technical Skills
Scientific Writing
Medical Review
Medical Affairs
Medical Information
Medical Communications
MLR Review
Literature Review & Data Analysis
Clinical Trial Interpretation
Pharmaceutical Compliance
Regulatory Review
Content Quality Check (QC)
Software & Platforms
Veeva Vault PromoMats
Veeva MedComms
Microsoft Office Suite
Adobe Acrobat
Scientific Databases (PubMed, Ovid, Embase)
Core Competencies
Strong communication skills
Excellent proofreading abilities
Attention to detail
Project management expertise
Ability to manage multiple therapeutic areas
Regulatory understanding of pharmaceutical promotional practices
Therapeutic Areas Covered
Candidates may work across multiple therapeutic domains including:
Oncology
Hematology
Immunology
Rare Diseases
Cardiology
Dermatology
Gastroenterology
Neurology
Infectious Diseases
Nephrology
Respiratory
Endocrinology
Women’s Health
Ophthalmology
Rheumatology
Hepatology
Preferred Candidate Profile
EVERSANA is looking for professionals who are:
Scientifically driven
Ethical and detail-oriented
Strong collaborators
Adaptable learners
Results-focused
Skilled in interpreting complex medical data
Comfortable working in global matrix environments
Work Schedule & Travel
Average Working Hours: 40+ hours/week
Travel Requirement: Up to 10%
Why Join EVERSANA?
Global Exposure
Work with international pharmaceutical and biotech clients across diverse therapeutic areas.
Career Growth
Gain exposure to Medical Affairs, Regulatory Affairs, Scientific Communications, and Global Medical Review operations.
Remote Flexibility
Employees can work remotely while collaborating with global healthcare teams.
Innovation-Driven Culture
EVERSANA promotes innovation, diversity, transparency, and professional development.
Keywords for Job Seekers
Medical Reviewer Jobs in Pune, Scientific Reviewer Jobs in India, Medical Affairs Jobs, MLR Review Jobs, Medical Communications Careers, Pharmacovigilance and Medical Writing Jobs, Scientific Writing Jobs in Pharma, Veeva Vault Jobs, Pharma Remote Jobs India, Medical Information Specialist Jobs, Pharmaceutical Regulatory Review Careers, Healthcare Content Reviewer Jobs.
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