As a Senior CRA I, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets. You will have the opportunity to work on clinical studies in various therapeutic areas and indications while maintaining the highest quality standards in the industry. This function operates at site and country level and can be assigned to projects as monitor or lead monitor.
Join the PSI team and help drive innovation and excellence in advancing healthcare solutions.
You will:
- Prepare, conduct and reports site selection, initiation, routine monitoring and close-out visits
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Act as a communication point between project teams and the site
- Leads project team calls on a country level
- Ensure that subject recruitment targets are timely defined, communicated, recorded and met, and project timelines are followed at site level
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
- Prepare and participate in site audits and inspections