Job Title: Documentation/Medical Writing
No. of Posts: 1
he Medical Writing Associate will assist the Lead Medical Writer in creating and updating clinical research documents viz. Investigators Brochure, Patient Information Sheet & Informed Consent Forms, Clinical Study Reports. Will be responsible for registration and updating records for clinical trial registries. Will track induction training and ongoing training records for the Clinical team. Will be responsible for maintaining compliance and represent Clinical Science team during internal audits.
Writing clinical study reports, clinical reviews and informed consent form
Preparing and updating Investigators brochures
Registering clinical trials on registry
Writing clinical study documents within given timeline
Maintaining quality of the documents and adherence to the guidelines
Past experience in writing clinical development documents, registering clinical trials, maintaining trackers for quality compliance is preferable. Good written and spoken English, ability to coordinate and work with teams is a must
Qualifications: M.Pharm with minimum 3-7 yrs of experience required.