EDUCATION:

• Associate or Bachelor’s degree required; degree in life sciences or healthcare field preferred.

EXPERIENCE:

• 3–5 years of experience in clinical research, clinical trials, or FDA-regulated healthcare environment.

KNOWLEDGE, SKILLS AND ABILITIES

• Strong knowledge of clinical documentation requirements and trial operations.
• Skilled in Microsoft Office (Excel, Word, PowerPoint, Outlook); proficiency with EDC or clinical databases strongly preferred.
• Excellent organizational skills with the ability to manage multiple priorities in a fast-paced environment.
• Strong attention to detail, accuracy, and follow-through.
• Clear communicator who builds positive working relationships with internal teams, sites, and vendors.
• Demonstrated commitment to a coordinator-level role as a valued and stable contributor.

ROLE OVERVIEW:

The Clinical Coordinator provides experienced administrative and logistical support to the Clinical Operations team. This role manages a broad range of trial coordination activities—from image and data tracking to documentation, payments, device logistics, and meeting support. The position flexes across responsibilities based on team workload, ensuring studies run smoothly and are audit-ready. The Clinical Coordinator is a key, stable member of the Clinical Operations group and valued as a peer to other coordinators.