Regulatory and Start Up Specialist
IQVIA
full-time
Posted on:
Location Type: Office
Location: Tel Aviv • Israel
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Tech Stack
About the role
- Perform tasks at a country level associated with Site Activation (SA) activities
- Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites
- Ensure adherence to standard operating procedures (SOPs)
- Prepare site regulatory documents, reviewing for completeness and accuracy
- Review and provide feedback to management on site performance metrics
Requirements
- Bachelor’s Degree in life sciences or a related field
- 3 years’ clinical research or other relevant experience
- In-depth knowledge of clinical systems, procedures, and corporate standards
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
- Understanding of regulated clinical trial environment
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 researchsite activationregulatory document preparationperformance metrics reviewGCPICHclinical systems knowledge
Soft Skills
communicationattention to detailfeedback provisionorganizational skills