Senior Clinical Trials Associate
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Job Description
Senior Clinical Trials Associate providing administrative support to clinical project teams at Worldwide Clinical Trials. Focusing on documentation quality control and team coordination responsibilities.
Responsibilities:
- Provide administrative and project tracking support to the clinical project team
- Arrange and track system access for project team
- Maintain and quality audit to assure the most recent revisions of documents are on project portals
- Assist project team with preparation and shipment of clinical trial documentation
- Maintain version and quality control of project documentation
- Generate and distribute minutes for project related meetings
- Maintain current participating site and personnel information
- Assist with the interviewing, coaching, training and development of new employees
- Participate in special and complex projects to continuously improve processes
Requirements:
- Degree level qualification or equivalent experience
- Minimum of two years’ experience in a related role
- Strong attention to detail and quality of work
- Excellent written and verbal English skills
- Strong organizational and problem-solving skills
- Proficient in MS Office applications including Outlook, Word, Excel and PowerPoint
- Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
Benefits:
- Inclusive and diverse work environment
- Opportunities for professional development
- Training and coaching for new employees
- Collaborative team culture
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