Looking for Regulatory Medical Writing Trainee jobs in Gurgaon? DDReg Pharma has announced openings for Regulatory Medical Writing – Trainee positions for M.Pharm (Pharmacology) graduates. This is an excellent opportunity for fresh postgraduates and early-career professionals who want to build a career in medical writing, regulatory affairs, and pharmaceutical documentation.
The Regulatory Medical Writing Trainee role offers hands-on exposure to global regulatory documentation, literature review, clinical and non-clinical data analysis, and structured product labeling activities under the guidance of experienced professionals.
Job Details
- Position: Regulatory Medical Writing – Trainee
- Company: DDReg Pharma
- Department: Regulatory Affairs & Medical Writing
- Location: Gurgaon, Haryana, India
- Employment Type: Full-Time
- Experience: Freshers and early-career professionals
- Posted Date: 18 June 2026
Key Responsibilities
As a Regulatory Medical Writing Trainee, you will:
- Support drafting of prescribing information (PI) and structured product labeling (SPL) documents.
- Assist in preparing biowaiver justifications and bioequivalence (BE) templates.
- Contribute to clinical and non-clinical overviews and technical information files (TIF).
- Review clinical study reports, scientific literature, and source documents.
- Perform quality checks for regulatory and medical writing documents.
- Support gap analysis activities for small molecules and biosimilars.
- Assist in preparing responses to regulatory and client queries.
- Conduct literature searches and manage references for documentation activities.
- Learn and apply global regulatory guidelines and documentation standards.
- Maintain project trackers, document version control, and progress reports.
- Communicate project updates and challenges effectively with supervisors.
Educational Qualification
Required Qualification:
- M.Pharm (Pharmacology) – Only
Candidates from other specializations may not be considered for this role.
Required Skills
Candidates should possess:
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Excellent written and verbal English communication skills
- Strong attention to detail
- Ability to meet project deadlines
- Good analytical and scientific writing capabilities
- Proactive learning attitude and adaptability
Why Join DDReg Pharma?
This Regulatory Medical Writing Trainee position offers:
- Exposure to global regulatory documentation standards
- Training in medical writing and regulatory affairs processes
- Experience working on pharmaceutical submissions and labeling projects
- Opportunities to work on biosimilars and small molecule regulatory activities
- Professional mentorship from experienced regulatory professionals
- Career growth opportunities in pharmaceutical regulatory affairs and medical writing
Work Environment
The selected candidates may occasionally work in schedules catering to different global time zones depending on project requirements.
Job Location
Gurgaon, Haryana, India
Estimated Salary
Based on industry standards for entry-level regulatory medical writing positions:
Estimated CTC: ₹3.0 – ₹5.0 LPA
Actual compensation may vary based on qualifications, skills, and company policies.