Clinspire CR has announced an exciting opportunity for talented candidates who are passionate about scientific writing, clinical research, and regulatory documentation. The company is inviting applications from Freshers with excellent scientific writing skills as well as professionals with 1–5 years of experience in medical writing or clinical research.
This Medical Writer job in Varanasi is an excellent opportunity for Pharm.D, M.Pharm, Pharmacy, Life Sciences, Biotechnology, Medicine, and related graduates seeking a rewarding career in clinical research and regulatory writing.
Job Highlights
| Particular | Details |
|---|---|
| Position | Medical Writer |
| Company | Clinspire CR |
| Location | Varanasi, Uttar Pradesh |
| Experience | Freshers & 1–5 Years |
| Qualification | Bachelor’s, Master’s, Pharm.D, M.Pharm, Pharmaceutics, Life Sciences, Biotechnology, Medicine or related field |
| Employment Type | Full-Time |
| Application Mode |
Medical Writer Job Responsibilities
As a Medical Writer at Clinspire CR, you will:
- Prepare and review Clinical Study Protocols.
- Draft Clinical Study Reports (CSRs).
- Develop Investigator Brochures and Informed Consent Forms.
- Prepare scientific and regulatory documents according to ICH-GCP guidelines.
- Conduct literature searches and summarize scientific evidence.
- Collaborate with Clinical Operations, Regulatory Affairs, Biostatistics, and Project Management teams.
- Ensure documentation accuracy, consistency, and regulatory compliance.
- Deliver high-quality documents within project timelines.
Eligibility Criteria
Applicants should possess one of the following qualifications:
- Bachelor’s Degree
- Master’s Degree
- Pharm.D
- M.Pharm
- Pharmaceutics
- Life Sciences
- Biotechnology
- Medicine
- Other related healthcare or life science disciplines
Experience
- Freshers with excellent scientific writing skills can apply.
- 1–5 years of experience in Medical Writing or Clinical Research is preferred.
Preferred Skills
Candidates having the following skills will have an advantage:
- Strong knowledge of ICH-GCP Guidelines
- Understanding of CONSORT Guidelines
- Regulatory writing standards
- Scientific literature review
- Excellent English communication skills
- Microsoft Office proficiency
- Analytical thinking
- Attention to detail
- Time management
- Team collaboration
Why Join Clinspire CR?
Working as a Medical Writer offers opportunities to:
- Build a career in Clinical Research and Regulatory Affairs.
- Work on international clinical documentation.
- Gain exposure to scientific publications and regulatory submissions.
- Collaborate with experienced clinical research professionals.
- Enhance scientific writing and documentation expertise.
- Grow within a dynamic and research-driven organization.
How to Apply
Interested candidates should send their updated CV to:
📧 Email: clinspirecr@gmail.com