Clinical Research Coordinator (Onsite)

Shift : M-F 7am to 4pm hours may be adjusted by Hiring Division Director

Position Summary:
The Research Coordinator is responsible for managing multiple clinical research protocols while serving as a key liaison between site investigators and sponsors. This role operates under direct supervision and is designed to develop expertise in clinical research operations, compliance, and patient protection.

Key Responsibilities:

• Coordinate daily operations of research studies from feasibility through closeout.

• Act as liaison between site personnel, sponsors, and supervisors.

• Collaborate with finance, hospital administration, and IRB (if applicable).

• Schedule and track assessments and study milestones.

• Review study protocols with physicians and patients to ensure eligibility compliance.

• Ensure proper informed consent and adherence to protocol and regulatory standards.

• Enter and verify clinical data in Case Report Forms or electronic systems.

• Create source documentation tools when not provided by sponsors.

• Monitor and report adverse events, protocol deviations, and waivers.

• Manage study supplies, including drug and device shipments.

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

• Respond to monitoring and audit findings.

Education & Experience:

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

• Preferred: Certified Clinical Research Coordinator (CCRC).

Knowledge, Skills & Abilities:

• Knowledge:

  • Basic clinical research operations, ICH-GCP guidelines, and federal regulations.

  • Understanding of medical terminology and internal SOPs.

• Skills:

  • Effective communication and time management.

  • Clinical trial skills such as ECG acquisition, phlebotomy, and specimen handling.

• Abilities:

  • Strong attention to detail, self-motivation, and interpersonal skills.

  • Ability to manage multiple tasks in a regulated environment.

Clinical Competencies:

Annual demonstration of clinical skills (e.g., ECG, specimen processing) may be required. Training and certification will be provided as necessary per protocol.

Travel Requirements:

Occasional Travel (up to 25%)
No Travel
50% or more

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.