Senior Medical Writer II ProPharma India job 2026. Check eligibility, experience, responsibilities, and apply online for regulatory writing career opportunity today.
Introduction
Are you an experienced medical writer looking to advance your career in clinical research and regulatory writing? The Senior Medical Writer II at ProPharma offers a high-impact role where you will work on complex clinical and regulatory documents across global projects. This opportunity is ideal for professionals with strong expertise in medical writing, data interpretation, and regulatory submissions.
With growing demand for regulatory writing jobs in India, this position provides a chance to collaborate with global teams and contribute to critical drug development programs.
Job Overview
| Details | Information |
|---|---|
| Job Title | Senior Medical Writer II |
| Company Name | ProPharma |
| Location | India (Remote / Hybrid) |
| Employment Type | Full-Time |
| Department | Medical Writing / Clinical Research |
| Experience Required | Minimum 6 Years |
| Education | Bachelor’s or Higher in Life Sciences |
| Salary | As per company standards |
Company Overview
ProPharma is a globally recognized partner for pharmaceutical, biotechnology, and medical device companies. With over 20 years of industry expertise, the company provides comprehensive solutions in clinical research, regulatory affairs, pharmacovigilance, and medical information.
By supporting the complete product lifecycle—from early research to regulatory approvals—ProPharma helps organizations deliver safe and effective therapies worldwide.
Job Location & Employment Type
This role is open to candidates across India and primarily supports remote working, with an option for hybrid collaboration depending on proximity to company offices.
- Employment Type: Full-Time
- Work Mode: Remote / Hybrid
Open Positions / Department Details
- Role: Senior Medical Writer II
- Department: Medical Writing
- Job ID: JR 7810
- Industry: Clinical Research / CRO / Pharma
Key Roles & Responsibilities
As a Senior Medical Writer II at ProPharma, you will be responsible for delivering high-quality clinical and regulatory documents:
- Author and edit complex medical writing deliverables such as:
- Clinical study reports
- Protocols and amendments
- Investigator brochures (IBs)
- Regulatory submissions (IND, NDA, BLA, MAA)
- Safety reports and summaries
- Ensure compliance with global regulatory guidelines (ICH, FDA, EU MDR/IVDR)
- Manage timelines, budgets, and client expectations
- Collaborate with cross-functional teams including biostatistics, data management, and regulatory affairs
- Conduct peer reviews and quality checks of documents
- Mentor and guide junior medical writers
- Participate in client meetings and project discussions
- Maintain audit trails and document consistency
- Contribute to process improvements and team initiatives
Eligibility Criteria
Educational Qualification
- Bachelor’s degree or higher in:
- Life Sciences
- Medical or Scientific disciplines
Experience Required
- Minimum 6 years of experience in:
- Clinical or regulatory medical writing
- CRO, pharmaceutical, or biotechnology companies
Skills Required
- Advanced knowledge of clinical research and regulatory requirements
- Strong understanding of submission documents (IND, NDA, BLA, etc.)
- Excellent writing, editing, and communication skills
- Proficiency in MS Word (tables, graphs, formatting)
- Ability to interpret complex clinical and statistical data
- Strong project management and time management skills
- Familiarity with AMA style and regulatory guidelines
Salary & Benefits
- Salary: As per company standards
- Performance-based bonuses
- Remote working flexibility
- Health and wellness benefits
- Career growth with internal promotions
- Learning and development programs
- Opportunity to work on global regulatory projects
Selection Process
The recruitment process typically includes:
- Online application submission
- Screening by recruitment team
- Technical/functional interview
- Final interview with hiring manager
- Offer and onboarding
- Expected timeline: 3–6 weeks
How to Apply
Interested candidates should apply through the official online application portal by submitting their updated CV and relevant documents.
Important Dates
- Application Deadline: Not specified (Apply early recommended)
Why Apply for This Job?
The Senior Medical Writer II ProPharma job is a premium opportunity because:
- Work on high-level global regulatory submissions
- Collaborate with experienced international teams
- Gain exposure to multiple therapeutic areas
- Strong career growth into leadership roles
- Flexible remote working environment
- Opportunity to mentor and lead projects
FAQs
1. Who can apply for this job?
Candidates with a life sciences or medical degree and at least 6 years of medical writing experience can apply.
2. Is this role suitable for freshers?
No, this is a senior-level role requiring significant experience.
3. What type of documents will I work on?
You will work on clinical, regulatory, and safety documents including IND, NDA, and clinical study reports.
4. Is this a remote job?
Yes, it is primarily remote with optional hybrid work.
5. What skills are essential?
Advanced medical writing, regulatory knowledge, data interpretation, and project management skills are essential.
Conclusion
The Senior Medical Writer II at ProPharma is an excellent opportunity for experienced professionals aiming to excel in regulatory and clinical writing. With global exposure, flexible working options, and strong career growth, this role offers everything needed to advance in the medical writing field. Apply now to take your career to the next level.
Disclaimer
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