Apply for Medical Writing Program Manager at Thermo Fisher Scientific 2026. Check eligibility, salary, responsibilities, and online application process details here.
Introduction
If you are an experienced medical writer or clinical research professional looking to step into leadership, this opportunity can be a strong career move. The Medical Writing Program Manager role at Thermo Fisher Scientific offers a chance to manage global clinical documentation projects while working remotely. With increasing demand in regulatory writing and publishing, this role is ideal for candidates aiming for senior-level growth in the pharmaceutical industry.
Job Overview
| Details | Information |
|---|---|
| Job Title | Medical Writing Program Manager (QC & Publishing Lead) |
| Company Name | Thermo Fisher Scientific |
| Location | Bangalore, Karnataka, India (Remote) |
| Employment Type | Full-Time |
| Department | Clinical Research / Medical Writing |
| Experience Required | 8+ Years |
| Education | Bachelor’s in Life Sciences (Advanced Degree Preferred) |
| Salary | As per company norms |
Company Overview
Thermo Fisher Scientific is a globally recognized leader in scientific research services, laboratory solutions, and clinical development. Through its PPD clinical research division, the company supports pharmaceutical and biotech firms in bringing new treatments to market faster. With operations across 100+ countries, it provides innovative solutions in drug development, clinical trials, and regulatory support.
Job Location & Employment Type
This role is based in Bangalore, India, but offers a fully remote working model, making it suitable for professionals across India. It is a full-time permanent position under the clinical research services segment.
Open Positions / Department Details
The opening is within the Medical Writing Functional Service Provider (FSP) team, focusing on document quality control and publishing leadership. The selected candidate will act as a central coordinator between clients and internal teams, ensuring smooth delivery of regulatory documents.
Key Roles & Responsibilities
- Lead and oversee document review and publishing activities for clinical projects
- Manage project timelines, deliverables, and forecasting
- Serve as the primary contact for client communication and issue resolution
- Monitor project risks related to timelines, quality, and budget
- Ensure consistency and compliance with regulatory and quality standards
- Review clinical and regulatory documents such as CSR, Protocols, IB, and ICF
- Train and mentor team members involved in document review processes
- Develop performance metrics and track project efficiency
- Allocate resources effectively to meet deadlines and project demands
- Support continuous improvement in documentation and publishing workflows
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Pharmacy, or related scientific field
- Advanced qualifications (M.Pharm, MSc, PhD) are preferred
- Certifications like AMWA, EMWA, or RAC are considered an advantage
Experience
- Minimum 8 years of relevant experience in medical writing or document review
- Experience in handling regulatory documents such as CSR, Protocols, and IB
- Prior exposure to CRO or pharmaceutical industry is desirable
- Experience in project management or team leadership is preferred
Skills Required
- Strong medical writing and editing skills
- Excellent project management and planning abilities
- Knowledge of global regulatory guidelines and documentation standards
- Effective communication and stakeholder management skills
- Leadership and mentoring capabilities
- High attention to detail and quality control
- Ability to work under tight deadlines
Salary & Benefits
- Salary: As per company norms
- Flexible remote working environment
- Health and wellness benefits
- Learning and development programs
- Career growth opportunities in global clinical research
- Collaborative and inclusive work culture
Selection Process
The selection process generally includes:
- Application screening
- HR interview
- Technical/functional interview
- Final discussion with leadership or client team
How to Apply
Interested candidates can apply through the official online application portal of the company. Ensure your resume highlights your experience in medical writing, regulatory documentation, and project management.
Important Dates
- Application Start Date: Already Open
- Last Date to Apply: Not specified (Apply as soon as possible)
Why Apply for This Job?
This role offers a unique opportunity to work at the intersection of medical writing, project management, and client leadership. As a Program Manager, you will gain exposure to global clinical trials and regulatory submissions. The remote work model adds flexibility, while the leadership responsibilities help accelerate your career growth. If you are aiming for senior roles in CROs or pharmaceutical companies, this position can significantly strengthen your professional profile.
FAQs
1. What is the required experience for this role?
Candidates need at least 8 years of experience in medical writing or document review.
2. Is a master’s degree mandatory?
No, but an advanced degree is preferred and can improve your chances.
3. What type of documents will I handle?
You will work on CSR, Protocols, Investigator Brochures (IB), and informed consent forms (ICF).
4. Is this a remote job?
Yes, the role is fully remote, although based in Bangalore.
5. What is the salary range?
The salary is not disclosed and will be as per company standards.
Conclusion
The Medical Writing Program Manager role at Thermo Fisher Scientific is a high-level opportunity for experienced professionals in clinical research and regulatory writing. With global exposure, leadership responsibilities, and flexible working conditions, it is an excellent option for career advancement in the pharma sector. Interested candidates should apply early to secure their chance.
Disclaimer
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