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Research Staff Jobs in Connecticut

1 - 14 of 14
1 - 14 of 14
Search Results - Research Staff Jobs in Connecticut
ProTouch Staffing-Greenwich (CT)-
and oversee study procedures  •  Ensure adherence to GCP and regulatory standards  •  Review safety data, AEs/SAEs, and documentation in EHR/EDC  •  Collaborate with sponsors, CROs, and research staff Requirements:  •  M.D./D.O. with active Connecticut medical...
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ProTouch Staffing-Greenwich (CT)-
examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document patient...
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ProTouch Staffing-Greenwich (CT)-
and physical examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document...
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ProTouch Staffing-Greenwich (CT)-
examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document patient...
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ProTouch Staffing-Greenwich (CT)-
participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document patient interactions, monitor adverse...
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ProTouch Staffing-Greenwich (CT)-
examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document patient...
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ProTouch Staffing-Greenwich (CT)-
specialty assessments, and physical examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial...
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ProTouch Staffing-Greenwich (CT)-
examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document patient...
Read more
ProTouch Staffing-Greenwich (CT)-
and physical examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document...
Read more
ProTouch Staffing-Greenwich (CT)-
and physical examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document...
Read more
ProTouch Staffing-Greenwich (CT)-
and physical examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document...
Read more
ProTouch Staffing-Greenwich (CT)-
and physical examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document...
Read more
ProTouch Staffing-Greenwich (CT)-
and physical examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document...
Read more
ProTouch Staffing-Greenwich (CT)-
and physical examinations.  •  Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards.  •  Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution.  •  Document...
Read more

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