Parexel

Senior Clinical Research Associate - FSP

Parexel

full-time

Posted on:

Location Type: Remote

Location: South Korea

Visit company website

Explore more

✨ AI Apply
Apply

Job Level

Senior

Tech Stack

Google Cloud Platform

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
  • Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators

Requirements

  • Minimum 3 years relevant experience in clinical research site monitoring
  • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
  • Fluent in English and in the native language(s) of the country they will work in
  • Bachelor's degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Benefits
  • Health insurance
  • Professional development opportunities
  • Significant travel is required
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical trial monitoringstudy monitoring plan (SMP)GCPsite activationdatabase lockenrollment supportrecruitment issue resolution
Soft Skills
communicationproblem-solvingorganizational skills