Job Description
Location:
HealthTrust Workforce Solutions External - CCST
Pay Rate: Hourly - Hourly Plan, 25.00 USD Hourly
Work Shift: 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
Job Tags
Hourly pay, Full time, Local area, Shift work,