Clinical Coordinator

Benefits

Qualifications

• •Bachelor's degree with a scientific background and three to five years' related experience required
• •Effective interpersonal communication skills and time management skills essential
• •Training and/or certification as a clinical research coordinator, such as Good Clinical Practices (GCP), or the ability to obtain

Responsibilities

• •Coordinate and manage clinical research protocols for the Vaccine Testing Center (VTC) within the Department of Microbiology and Molecular Genetics
• •Serve as a key liaison among investigators, sponsors, regulatory bodies, and clinical partners
• •Support study start-up, implementation, and closeout activities with a primary focus on the day-to-day, clinic-based operations of assigned studies
• •This includes coordinating participant visits, supporting recruitment and enrollment, and collaborating with the clinical team to ensure smooth study execution
• •Prepare regulatory submissions and study documentation
• •Support study operations, data quality, and participant safety by coordinating study activities, maintaining study records, and adhering to protocol requirements
• •Contribute to improving processes and assist with training of new staff as needed
• •Minimum Qualifications (or equivalent combination of education and experience)
• •5 more items(s)