Are you an experienced Medical Writer seeking to advance your career in the clinical research industry? Clinica Research is hiring skilled professionals for its Navi Mumbai office-based position. If you have hands-on expertise in preparing clinical trial documentation for Phase II–IV studies, this opportunity is for you.
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🧠 Position Details
- Designation: Medical Writer
- Location: Navi Mumbai, Maharashtra (Office-based)
- Experience: Minimum 2 years in regulatory medical writing for Phase II–IV clinical trials
- Employment Type: Full-time
📌 Key Responsibilities
As a Medical Writer at Clinica Research, you will be responsible for:
- Drafting and reviewing clinical study protocols for Phase II–IV trials.
- Preparing Informed Consent Forms (ICF) and ensuring ethical compliance.
- Writing and finalizing Clinical Study Reports (CSR).
- Developing other regulatory documents in alignment with ICH-GCP guidelines.
- Collaborating with clinical, regulatory, and project management teams to deliver high-quality documentation.
✅ Required Qualifications
- Educational Background: M.Pharm, MSc (Life Sciences), MBBS, or equivalent degree.
- Experience: Minimum 2 years of regulatory medical writing experience in clinical trials.
- Skills:
- Strong command over English language (written & verbal).
- Proficiency in regulatory guidelines (ICH-GCP, EMA, USFDA).
- Ability to manage timelines and multiple projects.
- Note: Freshers are not eligible for this role.
🌟 Benefits of Joining Clinica Research
- Competitive salary package (₹5,00,000 – ₹8,00,000 per annum).
- Exposure to high-impact global clinical research projects.
- Collaborative and growth-oriented work environment.
- Opportunity to enhance regulatory documentation expertise.
📩 How to Apply
Eligible candidates can apply by sending their updated CV to:
👉 Email: hr@clinicaresearch.com
📌 Subject Line: “Medical Writer Application”
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