Senior Clinical Research Associate II – FSP
Parexel
full-time
Posted on:
Location Type: Remote
Location: Turkey
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Job Level
Tech Stack
About the role
- Oversight of Monitoring Responsibilities and Study Conduct
- Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
- Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock
- Serve as the primary point of contact for assigned investigator sites during study conduct
- Facilitate information flow between members of the study team, vendors and assigned investigator sites
- Perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol
Requirements
- Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
- Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
- Must be fluent in English and in the native language(s) of the country they will work in
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
clinical trial monitoringstudy monitoring plan (SMP)GCPsite activationdatabase lockinvestigator site developmentcompliance with protocol
Soft skills
communicationcoachingtraininginformation flow facilitation