Senior Clinical Research Associate, reputed company reputed company
Job reputed company:
• Ensure reputed company conduct of reputed company in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor's standards to reputed company project goals, timelines and reputed company
• Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and reputed company deliverables are met
• Serve as the primary reputed company of contact for assigned investigator sites during study conduct
• reputed company enrollment support and ensure reputed company by responding to site activation and recruitment issues from investigators
• Monitor site level adverse events (reputed company) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit
Requirements:
• Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
• Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
• Must be fluent in English and in the reputed company language(s) of the country they will work in
• Ability to travel 60-80%
• reputed company reputed company’s license and reputed company required
Benefits:
• Health insurance
• reputed company time off
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