About the Role
This role involves supporting clinical trial operations through data analysis, documentation review, and adherence to regulatory standards within a decentralized team structure.
Responsibilities
- Review clinical trial data for accuracy and completeness
- Ensure compliance with regulatory requirements and protocols
- Support monitoring activities for ongoing studies
- Collaborate with cross-functional teams on project deliverables
- Assist in the preparation of study-related documentation
- Track and report on trial milestones and timelines
- Identify discrepancies in case report forms
- Communicate findings to supervisory staff
- Maintain up-to-date knowledge of industry guidelines
- Participate in virtual team meetings and trainings
- Conduct source document verification remotely
- Assist in audit readiness activities
- Monitor data entry timelines across trial sites
- Escalate protocol deviations when identified
- Support investigator-initiated study efforts
- Follow standard operating procedures for data handling
- Contribute to process improvement initiatives
- Ensure confidentiality of participant records
- Coordinate with external vendors as needed
- Update tracking systems for monitoring visits
- Review informed consent forms for compliance
- Assist in onboarding new trial sites
- Generate routine status reports for management
- Respond to queries from clinical data managers
- Maintain detailed records of review activities
Compensation
Up to $75,000
Work Arrangement
Remote
Team
Collaborative remote environment
Job Number
3692B
Salary
Up to $75,000 annually
Location
Fully remote position
Industry
Clinical research and development
Experience Level
Entry to mid-level
Employment Type
Full-time
Application Instructions
Submit resume and job number 3692B for consideration
Work Model
100% remote, no travel required
Not specified
