Senior Clinical Research Associate at Everest
Job Description & How to Apply Below
In this pivotal role, you will leverage your extensive monitoring experience and in-depth knowledge of ICH-GCP guidelines. The Senior Clinical Research Associate position demands interaction with study Sponsors and investigational sites, ensuring adherence to regulatory standards. You will be responsible for conducting feasibility visits and comprehensive monitoring throughout the study timeline.
Key Responsibilities:
• Interact with study Sponsors to ensure alignment
• Perform site feasibility assessments and pre-study visits
• Conduct interim monitoring and site close-out visits
• Review and submit detailed quality monitoring reports
• Support training sessions for site personnel
Requirements:
• Bachelor's degree in Life Sciences required
• Minimum 4 years of clinical trial monitoring experience
• Strong knowledge of ICH-GCP guidelines
• Experience in Pain, Oncology, and CNS therapeutic areas
• Excellent communication and organizational skills
Focus on enhancing clinical research quality and compliance with Everest Clinical Research.
#J-18808-Ljbffr
Position Requirements
10+ Years
work experience
Note that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
Search for further Jobs Here:
×