Clinical Research Coordinator

Location:

HealthTrust Workforce Solutions External - CCST

Pay Rate:

Hourly - Hourly Plan, 25.00 USD Hourly

Work Shift:

Job Description

Responsibilities

Company Overview

HHS is a private, family-owned business dedicated to caring for its team members and providing honest, quality-driven customer service. Founded in 1975, HHS now supports nearly 1,000 customers across various sectors including healthcare and hospitality.

Position Summary

We are seeking a Clinical Research Coordinator I to join our team. This role is responsible for coordinating multiple research protocols and serving as a liaison between local investigators, sponsors, and site staff. Working under direct supervision, the Coordinator will gain a strong foundation in research operations, regulations, and human subject research.

Key Responsibilities

• Adhere to the organization’s Code of Conduct , Mission, and Values.
• Complete all assigned training requirements on time.
• Coordinate and perform routine operational activities for multiple research protocols.
• Serve as the primary liaison between site research personnel, sponsors, and supervisors.
• Collaborate with departments such as finance, hospital administration, and IRB (if applicable).
• Manage study schedules from feasibility submission through study closeout.
• Review study design and eligibility criteria with physicians and patients.
• Ensure patient safety by verifying informed consent procedures and compliance with protocols.
• Maintain data integrity by reviewing source documents, resolving missing or implausible data, and entering accurate information into case report forms or electronic systems.
• Create study-specific documentation tools when needed.
• Track drug/device shipments and ensure proper supply management.
• Report adverse events, serious adverse events, and protocol deviations in a timely manner.
• Attend investigator meetings, study-specific calls, and internal team meetings as required.
• Respond to monitoring and audit findings.

Education & Experience

• Bachelor’s degree required.
• 1+ year of relevant experience in clinical research (or equivalent combination of education/experience) required.
• Degree in a healthcare or science-related field preferred.

Licenses & Certifications

• Certified Clinical Research Coordinator (CCRC) preferred.

Knowledge, Skills & Abilities

Knowledge:

• Understanding of organizational policies, SOPs, and research systems.
• Basic knowledge of ICH guidelines, FDA regulations, and medical terminology.

Skills:

• Excellent written and verbal communication.
• Strong organizational and time management skills.
• Basic clinical trial procedures (ECG acquisition, phlebotomy, specimen handling/shipping).

Abilities:

• Strong interpersonal skills with a collaborative mindset.
• Self-motivated with a meticulous attention to detail.
• Ability to perform and be trained on clinical competencies as required.

Travel

• Occasional travel may be required.

Why Join Us?

This is an excellent opportunity to grow your career in clinical research while making a meaningful impact on advancing medical knowledge and improving patient outcomes. We provide comprehensive training, support, and the opportunity to develop into more advanced research roles.

Billing Identifier:

CC 3271 Hourly