Senior Clinical Research Associate – FSP
Parexel
full-time
Posted on:
Location Type: Remote
Location: Argentina
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Job Level
Tech Stack
About the role
- Responsible for site management, site monitoring and close-out of assigned clinical trials investigator sites
- Ensure patient safety and quality study execution in accordance with applicable prevailing laws, GCP, and client standards
- Manage investigator site relationships to ensure effective delivery of clinical trials
- Monitor site level adverse events and collaborate with the Drug Safety Unit
- Identify and resolve investigator site issues within required timeframes
Requirements
- Minimum 3 years relevant experience in clinical research site monitoring
- Extensive knowledge of clinical trial methodologies
- Must be fluent in English and in the native language(s) of the country they will work in
- Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
- Valid driver’s license and passport required
Benefits
- Health insurance
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial methodologiessite monitoringadverse event monitoringissue resolution
Soft Skills
relationship managementcommunicationproblem-solving
Certifications
valid driver's licensepassport