- Remote, India
- Remote
- Associate
- 2+ years
Responsible for driving clinical trial and project acceleration through scientific authoring, study support, remote site master file oversight, material shipment coordination, and technical system management.
Responsibilities
- Conducts remote support activities and study oversight to ensure compliance and data quality.
- Acts as a remote extension of the clinical team to identify and resolve or escalate study issues.
- Manages document transfer for data entry and/or corrections.
- Manages the real-time digital assembly, QC, and maintenance of the Study Master File (SMF/TMF).
- Ensures all internal documents adhere to Elanco guidelines and regulatory templates.
Requirements
- DVM
- PhD