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Scienceabode > Clinical Research Coordinator (Onsite)

Clinical Research Coordinator (Onsite)

Last updated: 2025/08/31 at 8:05 AM
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  • Permanent
  • United States
  • Posted 6 hours ago
Nesco Resource, LLC

Website Nesco Resource, LLC

Nesco Resource, LLC

Company : Nesco Resource, LLC

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

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%)


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.

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