Apply for Document Review Specialist II at Thermo Fisher Scientific 2026. Check eligibility, salary, experience, and online application process details now.
Introduction
The demand for skilled medical writing and document review professionals is rapidly growing in the pharmaceutical and clinical research industry. The Document Review Specialist II at Thermo Fisher Scientific is an excellent opportunity for candidates with experience in regulatory writing and quality control. This remote role allows professionals to work on global clinical projects while ensuring high-quality documentation standards.
Job Overview
| Details | Information |
|---|---|
| Job Title | Document Review Specialist II – Medical Writing |
| Company Name | Thermo Fisher Scientific |
| Location | Bangalore, Karnataka, India (Remote) |
| Employment Type | Full-Time |
| Department | Clinical Research / Medical Writing |
| Experience Required | 2+ Years |
| Education | Bachelor’s Degree in Life Sciences or related field |
| Salary | As per company norms |
Company Overview
Thermo Fisher Scientific is a leading global organization providing scientific solutions, laboratory services, and clinical research support. Through its PPD clinical research division, the company partners with pharmaceutical and biotechnology firms to accelerate drug development and ensure regulatory compliance. With a presence in over 100 countries, it is known for innovation, quality, and strong career development opportunities.
Job Location & Employment Type
This position is officially based in Bangalore, India, but offers a fully remote working model. It is a full-time role, making it suitable for candidates seeking stability and long-term growth in the clinical research domain.
Open Positions / Department Details
The role is part of the Medical Writing Functional Service Provider (FSP) team. The selected candidate will work closely with client-dedicated teams and contribute to reviewing and improving clinical and regulatory documents across multiple projects.
Key Roles & Responsibilities
- Review scientific and regulatory documents to ensure quality and compliance
- Validate data consistency in tables, figures, and listings against source documents
- Edit documents for grammar, clarity, and formatting accuracy
- Ensure adherence to regulatory guidelines and company templates
- Improve scientific language for better readability and audience understanding
- Collaborate with authors and stakeholders for clarification and improvements
- Handle urgent document reviews and meet tight deadlines
- Maintain updated knowledge of regulatory standards and industry practices
- Support operational efficiency through effective communication
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field
- Additional certifications in medical writing are an advantage
Experience
- Minimum 2 years of experience in medical writing or document review
- Experience with regulatory documents such as CSR, Protocols, IB, and ICF
- Exposure to CRO or pharmaceutical industry preferred
- Experience with document formatting tools like MS Word is desirable
Skills Required
- Strong attention to detail and analytical thinking
- Good understanding of medical terminology and clinical research concepts
- Knowledge of regulatory guidelines such as ICH and GCP
- Excellent English writing, editing, and proofreading skills
- Ability to manage multiple tasks and deadlines
- Strong teamwork and communication skills
- Familiarity with document management systems
- Ability to work independently in a remote environment
Salary & Benefits
- Salary: As per company norms
- Flexible work-from-home setup
- Health and wellness programs
- Learning and development opportunities
- Exposure to global clinical research projects
- Supportive and collaborative work culture
Selection Process
The hiring process typically includes:
- Resume shortlisting
- HR screening interview
- Technical assessment or interview
- Final discussion with the hiring team
How to Apply
Candidates interested in this opportunity can apply through the official online career portal of the company. Ensure your resume highlights your experience in regulatory writing, document review, and clinical research.
Important Dates
- Application Start Date: Open
- Last Date to Apply: Not specified
Why Apply for This Job?
The Document Review Specialist II at Thermo Fisher Scientific offers a strong foundation for professionals aiming to build a career in medical writing and regulatory affairs. This role provides hands-on experience with global clinical documents and exposure to international regulatory standards. The remote work model ensures flexibility, while the company’s structured training programs support continuous career growth.
FAQs
1. What is the minimum experience required?
At least 2 years of experience in document review or medical writing is required.
2. Is this job fully remote?
Yes, it is a remote role, although officially based in Bangalore.
3. What documents will I review?
You will work on clinical study reports, protocols, investigator brochures, and other regulatory documents.
4. Is prior CRO experience necessary?
It is not mandatory but preferred and can improve your chances.
5. What skills are most important for this role?
Strong editing, attention to detail, regulatory knowledge, and communication skills are essential.
Conclusion
The Document Review Specialist II role at Thermo Fisher Scientific is a valuable opportunity for early to mid-level professionals in medical writing. With global exposure, flexible work options, and career advancement potential, this role can significantly enhance your professional journey in the pharmaceutical industry. Apply early to maximize your chances.
Disclaimer
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