IQVIA has announced recruitment for the position of Medical Writer 1 in Bangalore and Thane, Maharashtra. This is an excellent opportunity for life sciences professionals with 1–3 years of medical writing experience who are looking to build a career in clinical research and regulatory medical writing.
As a Medical Writer at IQVIA, you will prepare high-quality clinical and regulatory documents, collaborate with cross-functional project teams, communicate with global clients, and contribute to the development of innovative medicines. Candidates with strong scientific writing skills, knowledge of clinical trials, and understanding of GCP guidelines are encouraged to apply.
| Details | Information |
|---|---|
| Company | IQVIA |
| Role | Medical Writer 1 |
| Job Type | Full-Time |
| Experience | 1–3 Years |
| Qualification | Bachelor’s in Life Sciences (Master’s/PhD Preferred) |
| Locations | Bangalore, Karnataka & Thane, Maharashtra |
| Last Date | 27 July 2026 |
| Job ID | R1559377 |
IQVIA is a global leader in clinical research, healthcare analytics, and commercial intelligence. The company supports pharmaceutical, biotechnology, and medical device organizations worldwide by accelerating drug development and improving patient outcomes through advanced technology, clinical expertise, and healthcare data solutions.
The selected Medical Writer will:
- Prepare clinical and regulatory documents according to IQVIA SOPs and client requirements.
- Lead straightforward medical writing projects independently.
- Prepare study protocols, clinical study reports (CSRs), and other regulatory documents.
- Coordinate document reviews with internal teams and clients.
- Manage project timelines and ensure timely document delivery.
- Resolve customer comments with support from senior medical writers.
- Participate in project meetings and client discussions.
- Monitor project budgets and forecast writing hours.
- Maintain compliance with GCP, regulatory guidelines, and company quality standards.
- Stay updated with developments in medical writing, clinical research, and drug development.
Applicants should possess:
Essential Qualification
- Bachelor’s Degree in Life Sciences or a related discipline.
Preferred Qualification
- Master’s Degree in Life Sciences
- PhD in Life Sciences
Experience
- 1–3 years of relevant Medical Writing experience.
Candidates should have:
- Strong knowledge of Clinical Study Reports (CSR)
- Experience with study protocols and regulatory documents
- Understanding of GCP and drug development process
- Knowledge of medical terminology
- Familiarity with statistical methods used in clinical trials
- Ability to interpret clinical data accurately
- Excellent scientific writing and grammar
- Strong communication and presentation skills
- Attention to detail
- Ability to manage multiple projects simultaneously
- Computer proficiency
Working at IQVIA offers professionals an opportunity to contribute to global healthcare innovation.
Benefits include:
- Global clinical research exposure
- International project collaboration
- Career growth in Medical Writing
- Learning and development opportunities
- Structured training programs
- Collaborative work environment
- Exposure to regulatory documentation
- Stable career with one of the world’s leading CROs
This opportunity is ideal for:
- Medical Writers
- Clinical Research Professionals
- Pharmacists
- Life Sciences Graduates
- Biotechnology Professionals
- Regulatory Writing Professionals
- Clinical Documentation Specialists
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