Clinical Research Coordinator: IRB/IACUC Projects

Oncology Voice Network LLC; Portsmouth (VA); On-site; USD 43,000 - 56,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) with company match

Paid time off

Professional development

Job summary

Goldbelt Apex LLC in Portsmouth, Virginia, seeks a Clinical Research Coordinator to support IRB/IACUC approved studies and QA projects. You will coordinate research activities across multiple departments, ensure protocol compliance, assist with consent, data reporting, and regulatory documentation, and support both human and non-human subjects research per applicable regulations.

You will collaborate with PIs, clinicians, and staff, manage scheduling, specimen handling, adverse event reporting,

Qualifications

• Excellent communication with senior government, clinical, scientific stakeholders.
• Strong written, verbal, organizational and interpersonal skills.
• Must be able to coordinate across departments and ensure protocol compliance.

Responsibilities

• Coordinate IRB/IACUC approved studies and NHSR projects.
• Assist with recruitment, consent, and screening of patients per protocol.
• Prepare and maintain regulatory documentation and reports for regulators.
• Support phlebotomy, specimen handling and data collection as required.
• Coordinate with PI to ensure resources and timelines are met.
• Communicate effectively with patients, staff and collaborating institutions.

Skills

Communication skills

Interpersonal skills

Education

Bachelor’s degree or higher

Job description

Goldbelt Apex LLC in Portsmouth, Virginia, seeks a Clinical Research Coordinator to support IRB/IACUC approved studies and QA projects. You will coordinate research activities across multiple departments, ensure protocol compliance, assist with consent, data reporting, and regulatory documentation, and support both human and non-human subjects research per applicable regulations.

You will collaborate with PIs, clinicians, and staff, manage scheduling, specimen handling, adverse event reporting,