Role OverviewPerform site monitoring visits, adapt and drive subject recruitment plans, administer protocol training, and evaluate study site practices. Work with sites to ensure compliance with study protocol, regulations, and sponsor requirements.
What You Will Do
Conduct site monitoring visits, track regulatory submissions, manage study progress, and ensure proper documentation. Collaborate with study team members for project execution support.
Why It Might Be a Fit
The ideal candidate will have experience in clinical research, knowledge of GCP and ICH guidelines, and strong therapeutic and protocol knowledge.
Requirements
- Bachelor's Degree in scientific discipline or health care
- At least 2 years of on-site monitoring experience
- Good knowledge of and skill in applying clinical research regulatory requirements
- Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Benefits
- Potential base pay range: $101,600.00 - $169,300.00
- Incentive plans, bonuses, and/or other forms of compensation
- Range of health and welfare benefits
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