Planet Pharma
Summary
To field monitor studies and data collection for clinical trials, assessing all data documentation, reports, records, transcripts and more.
Job Description Target PR Range: 50-60/hr.
Key Responsibilities
Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Committees, Clinical Operations (e.g., Contracts), and recommend and develop process improvements.
Verify trial/study data, including maintaining appropriate regulatory documents both internal and external, auditing to be sure the site has the appropriate regulatory documentation to conduct the trial/study, and source documentation is properly recorded.
Validate investigational device accountability by tracking the history of investigational devices from Edwards to the field sites and through final disposition.
Conduct onsite monitor visits.
Education and Experience
Bachelor's Degree or equivalent in related field
5-7 years of experience required
CO/NYC candidates might not be considered
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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Job Description Target PR Range: 50-60/hr.
Key Responsibilities
Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Committees, Clinical Operations (e.g., Contracts), and recommend and develop process improvements.
Verify trial/study data, including maintaining appropriate regulatory documents both internal and external, auditing to be sure the site has the appropriate regulatory documentation to conduct the trial/study, and source documentation is properly recorded.
Validate investigational device accountability by tracking the history of investigational devices from Edwards to the field sites and through final disposition.
Conduct onsite monitor visits.
Education and Experience
Bachelor's Degree or equivalent in related field
5-7 years of experience required
CO/NYC candidates might not be considered
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
#J-18808-Ljbffr