Clinical Research Coordinator (Onsite)

Research Coordinator

Position Summary:
The Research Coordinator is responsible for managing multiple clinical research protocols and serving as a liaison between investigators and sponsors. Under supervision, the role involves developing a solid understanding of research operations, regulations, and human subject protections.

Key Responsibilities:

• Coordinate daily operations of multiple research studies from feasibility to closeout.

• Serve as liaison among site personnel, industry sponsors, and supervisor.

• Collaborate with departments such as finance, hospital administration, and IRB.

• Assist in study setup, including assessments scheduling and review of eligibility criteria.

• Ensure patient safety and regulatory compliance through informed consent verification and adherence to protocol.

• Enter and manage accurate clinical data using study-specific tools or electronic systems.

• Monitor for data quality, protocol deviations, adverse events, and ensure timely reporting.

• Manage study supplies, including drug and device shipments.

• Attend site meetings, investigator calls, audits, and training sessions.

• Respond to monitoring findings and audit reports.

Education & Experience:

• Required: Bachelor's Degree and 1 year of relevant research experience (or equivalent education/experience).

• Preferred: Certified Clinical Research Coordinator (CCRC) certification.

Knowledge, Skills & Abilities:

• Knowledge:

  • Understanding of ICH-GCP, Code of Federal Regulations, and clinical research principles

  • Familiarity with medical terminology and clinical trial procedures

• Skills:

  • Strong organizational and time management skills

  • Effective verbal and written communication

  • Ability to perform basic clinical tasks (e.g., ECG, phlebotomy, specimen handling)

• Abilities:

  • Detail-oriented, self-motivated, and strong interpersonal skills

  • Ability to work independently and collaboratively in a team environment

Clinical Competency (as applicable):

Proficiency in basic clinical procedures may be required and assessed annually. Training and/or certification will be provided based on protocol needs.

Travel Requirement:

No Travel
Occasional Travel (up to 25%)