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: Bachelors 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.

Required Experience:

IC