Are you a pharmacy graduate with experience in Regulatory Affairs or Medical Writing and looking for an exciting opportunity in the clinical research industry? If yes, then Raptim Research Private Limited has announced multiple vacancies for experienced professionals at its Mahape, Navi Mumbai facility.
This recruitment drive is ideal for candidates who have worked on BA/BE studies, eCTD submissions, Clinical Study Reports (CSRs), and regulatory documentation. If you’re passionate about global regulatory compliance and scientific writing, this could be your chance to work with a reputed Contract Research Organization (CRO).
Let’s explore the complete details of the latest Raptim Research Recruitment 2026 including eligibility, job responsibilities, required experience, application process, and important tips for applicants.
📌 Raptim Research Recruitment 2026 – Overview
| Particular | Details |
|---|---|
| Organization | Raptim Research Private Limited |
| Industry | Clinical Research / CRO |
| Job Location | Mahape, Navi Mumbai, Maharashtra |
| Job Roles | Regulatory Affairs – Clinical & Medical Writing |
| Qualification | B.Pharm / M.Pharm |
| Experience Required | 1–4 Years |
| Employment Type | Full-Time |
| Application Mode | |
| Email Subject | Resume for Regulatory Affair |
🏢 About Raptim Research
Raptim Research is a well-established Contract Research Organization (CRO) that provides services in Bioavailability (BA), Bioequivalence (BE) studies, Clinical Trials, Regulatory Affairs, and Medical Writing.
The company supports pharmaceutical organizations by preparing regulatory submissions, managing clinical documentation, and ensuring compliance with international regulatory standards. Working at Raptim Research offers professionals exposure to global pharmaceutical regulations, clinical development, and high-quality research practices.
For candidates aiming to build a long-term career in regulatory affairs or medical writing, Raptim Research provides excellent learning opportunities in an international work environment.
💼 Open Positions
1️⃣ Regulatory Affairs – Clinical
This position is ideal for professionals who have experience preparing regulatory dossiers and handling clinical documentation for global submissions.
Key Responsibilities
✅ Prepare, review, and submit Clinical Module 5 dossiers.
✅ Compile Module 2.7 summaries for regulatory submissions.
✅ Prepare submissions in eCTD and NeeS formats.
✅ Review Clinical Study Reports (CSR) and study appendices.
✅ Coordinate responses to regulatory authority queries.
✅ Maintain submission lifecycle and tracking systems.
✅ Review CDISC datasets including SDTM and ADaM.
✅ Collaborate with Clinical Operations, QA, Biostatistics, Bioanalytical and Medical Writing teams.
✅ Ensure compliance with:
- ICH GCP
- ICH E6
- ICH M13
- eCTD Guidelines
- Global Regulatory Requirements
2️⃣ Medical Writing & Regulatory Affairs
Candidates who enjoy scientific writing and preparing clinical documents can apply for this role.
Responsibilities
The selected candidate will prepare and review:
- 📄 BA/BE Clinical Study Protocols
- 📄 Participant Information Sheets (PIS)
- 📄 Informed Consent Forms (ICF)
- 📄 Clinical Study Reports (CSR)
- 📄 Case Report Forms (CRFs)
- 📄 Electronic CRFs (eCRFs)
- 📄 Bioequivalence Summary Tables
Apart from documentation, the candidate will also coordinate with:
- Business Development Team
- Project Managers
- Principal Investigators
- Senior Management
The role also includes supporting departmental activities assigned by the reporting manager.
🎓 Educational Qualification
Applicants should possess any one of the following qualifications:
- ✅ B.Pharm
- ✅ M.Pharm (Pharmaceutics)
- ✅ M.Pharm (Pharmaceutical Sciences)
Candidates from recognized universities are eligible.
⏳ Experience Required
Applicants should have 1 to 4 years of relevant experience in:
- CRO
- Pharmaceutical Industry
- Regulatory Affairs
- Clinical Research
- Medical Writing
Freshers are not eligible for these positions.
📚 Required Technical Skills
Candidates having experience in the following areas will be preferred:
- eCTD submissions
- NeeS submissions
- Module 2.7 preparation
- Module 5 dossiers
- Clinical Study Reports
- BA/BE documentation
- ICH Guidelines
- CDISC
- SDTM
- ADaM
- Regulatory submissions
- Clinical documentation
- Global Health Authority submissions
💡 Essential Soft Skills
Apart from technical knowledge, candidates should possess:
- Excellent written English
- Strong communication skills
- Good documentation ability
- Attention to detail
- Analytical thinking
- Time management
- Teamwork
- Problem-solving skills
🌟 Why Join Raptim Research?
Working at Raptim Research provides professionals with opportunities to:
✔ Work on global regulatory submissions.
✔ Gain experience in international pharmaceutical projects.
✔ Improve expertise in clinical research.
✔ Learn advanced regulatory documentation.
✔ Collaborate with experienced professionals.
✔ Build a strong career in the CRO industry.
Professionals aiming for long-term growth in Regulatory Affairs or Medical Writing will find this opportunity highly valuable.
📩 How to Apply?
Interested candidates can apply by sending their updated resume through email.
Step 1
Update your CV with:
- Latest work experience
- Regulatory Affairs skills
- Medical Writing expertise
- Software knowledge
- Regulatory submission experience
Step 2
Use the following email subject:
Resume for Regulatory Affair
Step 3
Send your resume to:
📧 rakesh.talwatkar@raptimresearch.com
📧 purva.jadhav@raptimresearch.com
💡 Application Tips
Before sending your resume, mention:
- Current CTC
- Expected CTC
- Notice Period
- Preferred Role
- Total Experience
- Key Skills
A customised application generally improves the chances of being shortlisted.
📈 Career Scope in Regulatory Affairs
Regulatory Affairs remains one of the fastest-growing domains in the pharmaceutical industry. With increasing global regulatory requirements, companies continue to hire professionals skilled in dossier preparation, medical writing, and international submissions.
Professionals with expertise in eCTD, ICH Guidelines, Clinical Documentation, and BA/BE studies are increasingly sought after by CROs and pharmaceutical companies across India and overseas.
🔍 Who Should Apply?
This opportunity is suitable for:
- B.Pharm graduates with Regulatory Affairs experience
- M.Pharm professionals working in CROs
- Medical Writers
- Clinical Documentation Specialists
- Regulatory Submission Executives
- Professionals experienced in BA/BE studies
- Candidates looking for Navi Mumbai pharmaceutical jobs
🚀 Final Thoughts
The Raptim Research Recruitment 2026 presents an excellent opportunity for pharmacy professionals who want to strengthen their careers in Regulatory Affairs or Medical Writing. With exposure to international regulatory standards, clinical documentation, and global submissions, this role offers significant professional growth for candidates with relevant experience.
If you meet the eligibility criteria and have hands-on experience in clinical regulatory activities, don’t miss this opportunity. Update your resume, prepare a professional application, and apply at the earliest to maximize your chances of selection.
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