Clinical Trial Operations Specialist
17 hours ago
We are seeking a skilled Clinical Trial Operations Specialist to join our team at Parexel. This role is responsible for the delivery of clinical studies at allocated sites, ensuring compliance with international guidelines and local regulations.
Key Responsibilities:
- Site Management: Contribute to the selection of potential investigators, conduct site qualification visits, and ensure that sites are inspection ready at all times.
- Monitoring and Data Management: Perform monitoring visits, remote data checks, and source data verification in accordance with the Monitoring Plan.
- Compliance and Quality: Ensure compliance with Client Procedural Documents, ICH-GCP, and local regulations, and follow quality issue processes by escalating systematic or serious quality issues.
Requirements:
- Essential Skills: Excellent attention to detail, good written and verbal communication skills, and proficiency in written and spoken English language.
- Desirable Skills: Ability to work in an environment of remote collaborators, manage change with a positive approach, and demonstrate ability to prioritize and manage multiple tasks with conflicting deadlines.
Education: Bachelor's degree in a related discipline, preferably in life science, or equivalent qualification.
Estimated Salary: $60,000 - $80,000 per year, depending on experience and location.
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