JOB SUMMARY
The Senior Clinical Research Associate will support clinical studies and the Clinical Operations Department by managing various administrative tasks, including generating agendas and minutes, maintaining study tracking, and conducting filing and quality reviews. This role, reporting to the Clinical Operations department's leadership, will also involve participating in process improvement initiatives across departments. The Sr. CRA will be instrumental in collaborating cross-functionally, working closely with study teams from vendors and CROs to achieve departmental and project goals. The Sr. CRA must adhere to the company's core values and comply with all applicable regulations, ICH-GCP guidelines, and SOPs. Strong candidates should understand trial and study site management, vendor management, and experience participating in the full cycle of studies from start-up to close-out.KEY RESPONSIBILITIES:
QUALIFICATIONS:
ADDITIONAL REQUIREMENTS:
WE OFFER:
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