Clinical Research Coordinator 2 – Full Time

About the role

The Clinical Research Coordinator 2 (A) is a mid‑level professional who assists in planning, coordinating, implementing, monitoring and evaluating clinical research studies. The role manages day‑to‑day protocol operations from initiation through close‑out, ensuring compliance with regulatory and sponsor guidelines.

Key responsibilities

• Recruit, screen, and retain study participants, obtaining informed consent and scheduling visits.
• Perform study procedures, collect and record data, and process, pack and ship biological specimens according to protocol.
• Maintain study binders, regulatory files, and electronic data capture entries, meeting sponsor data‑lock deadlines.
• Distribute study drug materials, coordinate with the research pharmacy, and document unmasked records.
• Monitor adverse events, protocol deviations, and report to IRB and sponsors.
• Assist with protocol amendments, audits, and sponsor communications, and provide in‑service training to staff.

Required profile

• Bachelor’s degree in a relevant field.
• Minimum of 2 years of clinical research coordination experience.
• Ability to work evenings, nights and weekends as needed.
• Strong attention to detail, confidentiality, and ability to prioritize under pressure.
• Commitment to university core values and ability to work independently or collaboratively.

Required skills

• Proficiency with electronic data capture (EDC) systems.
• Specimen collection, processing and shipping expertise.
• Study drug dispensing and inventory management.

What we offer

• Competitive salary and comprehensive benefits package including medical, dental and tuition remission.