
Senior Clinical Research Associate – SE Region
Parexel
full-time
Posted on:
Location Type: Remote
Location: United States
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Job Level
Tech Stack
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