Senior Clinical Research Associate – FSP
Posted 61ds ago
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Job Description
Senior Clinical Research Associate at Parexel managing monitoring responsibilities and site conduct for clinical trials in the healthcare sector. Ensuring compliance with regulations and timelines while partnering with investigator sites.
Responsibilities:
- Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP)
- Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites
- Serve as the primary point of contact for assigned investigator sites
- Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
Requirements:
- Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
- Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
- Must be fluent in English and in the native language(s) of the country they will work in
Benefits:
- Health insurance
- Paid time off
- Flexible work arrangements
- Professional development















