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Under supervision, coordinates daily activities and operations of clinical research studies. Responsible for screening and enrolling patients, monitoring protocol implementation, completing required forms and reporting results, and regulatory submissions. Conducts data collection activities and may prepare analytical reports on study results. Follows established clinical study standards and procedures to plan and conduct clinical research studies. Maintain open communication with team members to ensure proper study progress.
Job Responsibility:
Coordinates daily activities and operations of clinical research studies
Screens and enrolls patients
Monitors protocol implementation
Completes required forms and reporting results
Conducts regulatory submissions
Conducts data collection activities
May prepare analytical reports on study results
Follows established clinical study standards and procedures
Maintains open communication with team members
Requirements:
Bachelor's degree in a science field required
0-1 years of experience required
What we offer:
flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement