Are you an experienced medical writer looking to contribute to impactful clinical research? Do you have a strong background in regulatory writing for clinical trials? If yes, we have an exciting opportunity for you in Navi Mumbai!
🧠 Position: Medical Writer
Location: Office-based, Navi Mumbai (Maharashtra)
Experience Required: Minimum 2 years in regulatory medical writing for Phase II–IV clinical trials
Clinica Research is currently hiring a Medical Writer to join our growing team of clinical research professionals. This is a full-time, office-based role that offers the chance to work on high-quality documentation for clinical trials and regulatory submissions.
🔍 Key Responsibilities
As a Medical Writer, you will be responsible for preparing and reviewing essential clinical trial documents, including:
Clinical Study Protocols
Informed Consent Forms (ICF)
Clinical Study Reports (CSR)
Other regulatory documents required for Phase II–IV trials
You will collaborate closely with clinical teams, regulatory affairs, and project managers to ensure that all documents meet regulatory standards and are delivered on time.
✅ Candidate Requirements
To be considered for this role, you must meet the following criteria:
Minimum 2 years of experience in regulatory medical writing
Strong understanding of clinical trial phases (II–IV)
Excellent written and verbal communication skills
Ability to work independently and manage multiple projects
Attention to detail and familiarity with ICH-GCP guidelines
Note: Freshers are kindly requested not to apply for this position. Only experienced candidates will be considered.
📩 How to Apply
If you meet the above qualifications and are ready to make a meaningful impact in the field of clinical research, we encourage you to apply.
📧 Send your updated CV to:
📌 Subject Line: Medical Writer Application
Please ensure your application includes a detailed CV highlighting your experience in regulatory writing and clinical documentation.
🌐 About Clinica Research
Clinica Research is a dynamic and fast-growing organisation dedicated to advancing clinical research through precision, ethics, and innovation. Our team is committed to producing high-quality documentation that supports regulatory compliance and scientific integrity.
By joining Clinica Research, you will be part of a collaborative environment that values expertise, continuous learning, and professional growth.
Are you ready to take the next step in your medical writing career? Apply today and become part of a team that’s shaping the future of clinical research.