Parexel is Hiring Medical Writer II
Under departmental supervision, the Medical Writer II will research, create, edit, and coordinate the production of clinical documents associated with submissions to regulatory authorities, including but not limited to: study protocols, model informed consents, interim and final clinical study reports, and safety update reports.
The Medical Writer II will also be responsible for the production of clinical study documentation associated with clinical trials that may not be included in a regulatory submission.
The Medical Writer II may serve as the primary client contact.
Bachelor’s degree in Life Sciences/Health Related Sciences or equivalent.