POSITION: SCIENTIFIC WRITER- CLINICAL RESEARCH

Role and Responsibility:

1. Responsible for medical writing activities that support the preparation of clinical trial documents (Phase-I-IV) in adherence to GCP and AXIS SOPs.

2. Manage the writing, editing and reviewing of diverse regulatory and clinical documents including clinical trial protocol, and amendments.

3. Review of statistical analysis plan

4. Preparation and review of investigator brochure, informed consent forms, and other clinical trial related documents.

5. Preparation and review of clinical study report (CSR).

6. Perform literature search/ reviews as necessary to obtain background information for development of clinical study documents.

Qualifications Required: Bachelor’s/ Master’s degree level in biological/ life science, pharmacy or other related background or equivalent medical qualification (2+ years experience).

Apply through below link

Scientific Writer-Clinical Research | AXIS Clinicals Ltd | LinkedIn