Psicro
Clinical Research Associate II
Remote, US, United States · Mid
Sponsorship not specifiedDetected 44 days ago
Clinical TrialsClinical ResearchResearchCommunicationCollaborationProblem SolvingMicrosoft Office
About the role
- We focus on delivering quality and on-time services across a variety of therapeutic indications.
- For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.
Nice to have
- Act as the main line of communication between the project team, sponsor, and the site
- Prepare, conduct, and report site selection, initiation, routine monitoring and close-out visits
- Ensure that subject recruitment targets are timely defined, communicated, recorded and met, and project timelines are followed at site level
- Ensure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations
- Ensure proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on sites
- Ensures quality (data integrity and compliance) at site level
- Conduct site audit preparation visits and resolve site audit findings
- Conduct project-specific training of site investigators
Visa & Work Authorization
- For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.
This listing is sourced directly from Psicro's careers page and normalized into a canonical job model.