Parexel

Senior Clinical Research Associate – SE Region

Parexel

full-time

Posted on:

Location Type: Remote

Location: United States

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Job Level

About the role

  • Actively participate in the local study team(s)
  • Contribute to the selection of potential investigators
  • Conduct Site Qualification Visits
  • Train, support, and advise Investigators and site staff
  • Ensure sites are always inspection ready
  • Perform monitoring visits (remote and onsite)
  • Manage study supplies, including drug accountability
  • Ensure compliance with local, national, and regional legislation
  • Prepares and finalizes monitoring visit reports
  • Provides timely feedback to the Principal Investigator

Requirements

  • SE Region - Oncology experience required
  • Excellent attention to detail
  • Good written and verbal communication skills
  • Good collaboration and interpersonal skills
  • Good negotiation skills
  • Proficient in written and spoken English language required
  • Fluency in local language(s) required
  • Excellent knowledge of international guidelines ICH-GCP
  • Basic knowledge of GMP/GDP
  • Good medical knowledge
  • Ability to understand the impact of technology on projects
  • Bachelor's degree in related discipline, preferably in life science
Benefits
  • Health insurance
  • 401(k) matching
  • Flexible working hours
  • Paid time off
Applicant Tracking System Keywords

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

Hard Skills & Tools
Oncology experienceSite Qualification VisitsMonitoring visitsDrug accountabilityMonitoring visit reportsInternational guidelines ICH-GCPGMPGDPMedical knowledgeTechnology impact understanding
Soft Skills
Attention to detailWritten communicationVerbal communicationCollaborationInterpersonal skillsNegotiation skills