- Perform all site monitoring visit activities, inclusive of all study visit types (PSV, SIV, IMV and COV)
- Participate in the site selection process with oversight from the Clinical Team Lead role
- Provide feedback to assist sites with resolution of detected deficiencies and corrective action needed, follow-up with sites until deficiencies are resolved
- Contribute to the development and review of protocols, study tools, and materials as well as documentation for clinical trials
- Provide mentoring, training, and co-monitoring of junior clinical team members
- Develop and maintain effective working relationships with clinical sites and within Rho as well as ensure communication of project goals and critical requirements
- Attend and present at meetings and conferences, including Investigator Meetings
- Participate in the RFP process, including business development meetings
- Participate in the Clinical Operations community at Rho by contributing to internal initiatives and standard operating procedures for the administration and monitoring of clinical trials
- Perform both onsite & remote monitoring and study closure activities across multiple protocols
MS Office