This role supports the successful execution of clinical trials by coordinating activities at research sites. The Clinical Research Coordinator II ensures study procedures are carried out according to protocol, sponsor requirements, and regulatory guidelines. Responsibilities include verifying source data, managing essential documents, and supporting site staff with training and compliance.
Key Responsibilities
- Conduct site initiation, monitoring, and close-out visits in line with study timelines
- Verify accuracy and completeness of clinical data through source document review
- Support site staff in understanding study protocols and regulatory expectations
- Maintain essential trial documents in compliance with SOPs and regulatory standards
- Identify and resolve site-level issues to maintain data integrity and patient safety
Qualifications
Candidates should hold a relevant degree in life sciences or healthcare and possess experience in clinical trial coordination. Strong organizational skills, attention to detail, and familiarity with regulatory requirements are essential. Experience with electronic data capture systems and site management processes is highly valued.
