Description
We are seeking a Clinical Research Site Manager to perform monitoring and site management work, ensuring sites conduct studies and report data as required by study protocols, regulations, and sponsor requirements.
The successful candidate will have a key role in:
- Performing site monitoring visits in accordance with contracted scope of work and Good Clinical Practice
- Working with sites to adapt, drive, and track subject recruitment plans
- Administering protocol and related study training to assigned sites
- Evaluating the quality and integrity of study site practices
- Managing study progress, tracking regulatory submissions and approvals, recruitment and enrollment, and data query generation and resolution
- Ensuring site documents are available for filing in the Trial Master File and verifying Investigator's Site File maintenance
- Creating and maintaining documentation regarding site management, monitoring visit findings, and action plans
- Collaborating with study team members for project execution support
The potential base pay range for this role, when annualized, is $90,200.00 - $190,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).
Benefits may include a range of health and welfare and/or other benefits, incentive plans, bonuses, and/or other forms of compensation.