**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

**Job Description**

**Job Description**

The Associate Medical Writer will work under the guidance and mentorship of experienced Medical Writers to support the timely delivery of high-quality clinical and regulatory documents. Responsibilities include contributing to the preparation of study protocols, clinical study reports (CSRs), investigator brochures (IBs), ICH M25/M27 documents, and other clinical, scientific, and regulatory documentation.

Key responsibilities include:

+ Support the development, editing, formatting, and quality review of clinical, scientific, and regulatory documents in accordance with client requirements, internal standards, and applicable regulatory guidelines.
+ Participate in project-related teleconferences and meetings, and coordinate meeting logistics as required.
+ Prepare and distribute meeting minutes, acti...