Psicro
Lead Clinical Research Associate
Remote, , Canada
Sponsorship not specifiedDetected 44 days ago
Project ManagementClinical TrialsClinical ResearchCRISPRResearchLeadershipCommunicationCollaborationProblem SolvingMentoringPublic SpeakingMicrosoft Office
About the role
- We focus on delivering quality and on-time services across a variety of therapeutic indications.
- All your information will be kept confidential according to EEO guidelines.
- 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
- Coordinates investigator/ site feasibility and identification process, as well as study startup.
- Reviews monitoring visit reports for all visit types and ensures reporting compliance of the Monitors in the region.
- Coordinates safety information flow and protocol/process deviation reporting.
- Ensures study-specific and corporate tracking systems are updated in a timely manner.
- Coordinates planning of supervised monitoring visits and conducts the visits.
- Ensures ongoing evaluation of data integrity and compliance at a country/regional level.
- Conducts site audit preparation visits, may participate in site audits, and coordinates resolution of site audit findings on a country/regional level.
- Oversees project team in CAPA development and implementation.
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.