Protocol / Medical Writer - Late Phase - Brillex Clinical Research Brillex Clinical Research Pvt. Ltd.

1.0 - 4.0 years

4 - 6 Lacs

gandhinagar, ahmedabad

Work from Office

Role & responsibilities 1. Responsible for clinical trial medical science related activities like preparation of protocol, Informed consent form, CRF, other study related documents and SOPs in line with ICH GCP, Indian and global regulatory. 2. Conduct relevant literature search for required for protocol and manuscript writing. 3. Ensures that medical writing deliverables conform to International Conference on Harmonization (ICH) and other relevant regulatory guidelines. 4. Ensure to follow all clinical and regulatory guidelines, processes and systems for medical science activities and ensure compliance to internal medical writing SOPs for Clinical trial. 5. Compiles, writes and edits medica...

Posted 17 hours ago

Apply

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.