Covance is seeking an Associate Medical Writer.
We are recruiting for our Medical Writing team in Madison, WI and are currently seeking to hire an Associate Medical Writer to help support the team. This is a full time position, based in our Madison, WI location. Remote work is not an option and must work onsite in our Madison, WI office.
About the Job
Within this position, your duties will include:
Responsible for preparation and review of clinical documents such as patient safety narratives and clinical study report (CSR) appendices. Responsible for preparing lower complexity documents such as synoptic or abbreviated CSRs under guidance of more senior staff. Assist Medical Writers in the preparation and background writing of clinical study protocols, CSRs, and subject narratives.
Ensure timely delivery of high quality documents to internal customers and Sponsors. Assist Medical Writers in the archiving and filing of clinical study protocols and CSRs and associated documentation. Foster excellent working relationships with all clients, both internal and external, with the highest quality of service in a cost-effective manner on time, every time. This position is for early phases of clinical development (e.g., Phase I through IIa studies focused on pharmacokinetics and pharmacodynamics).