Responsibilities
- Monitor and own the progress of clinical studies at investigative sites
- Ensure clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
- Coordinate all necessary activities required to set up and monitor a study
- Identify investigators
- Help prepare regulatory submissions
- Conduct pre-study and initiation visits
- Handle appropriately sized clinical trials
- Support Project Managers with trials that are larger in scope
- Train and mentor junior staff members
- Interact directly with clients
- Initiate payments
- Participate in proposal activities, including development and client presentations
Work Arrangement
Remote (Country)
Additional Information
- Position can be offered fully home based
- Domestic travel required up to approximately 50-60%, including overnight stays
- International travel may be required for some senior level positions
- Fluency in English required
- Local language fluency required for non-English speaking countries
- Application must be submitted in English
- Data provided in application will be stored in accordance with company policy
- Company is an Equal Opportunity Employer
- No unsolicited applications or third-party resumes accepted
- Beware of fraudulent job offers not associated with the company
