Clinical Research Coordinator: Trials, Compliance & Data

Evolution Research Group; Little Rock (AR); On-site; USD 52,000 - 78,000; Full time

Benefits offered by this job

Medical and dental coverage

401(k) matching

Paid time off

Job summary

Evolution Research Group (ERG) is a neuroscience-focused clinical development company providing Phase I–IV trial execution in the U.S. and globally.

The Clinical Research Coordinator will coordinate trials, ensure regulatory compliance, and manage subject enrollment under the PI and Site Director, while maintaining accurate documentation per FDA, GCP, and SOPs. The role requires understanding protocol requirements, informed consent, data capture, and ongoing communication with sponsors, IRBs,

Qualifications

• High School Diploma or equivalent; College degree preferred.
• Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.
• Knowledgeable in medical terminology to communicate with physician office and laboratory staff.
• Demonstrate initiative to act independently, initiate activity as required and make appropriate decisions within study protocols, regulatory requirements, and company policy.

Responsibilities

• Obtain detailed knowledge of all components of each study protocol through review and analysis with PI and Site Director prior to the effective date of the study.
• Assist to develop draft source documents and review documents for accuracy and clarity prior to study start up.
• Review with PI and Site Director any components needing additional information or clarification prior to initiation of the study.
• Manage studies with direct oversight to ensure compliance with protocol requirements.
• Collaborate with Recruitment Manager to develop programs for study enrollment.
• Contribute to SOP review and development as delegated by the Site Director.
• Perform study activities as delegated by the PI under Site Director supervision.
• Attend investigator meetings for assigned protocols as directed by Site Director.
• Ensure adherence to protocols and document breaches with sponsors and IRBs.
• Screen, enroll subjects and schedule visits with the PI.
• Review and obtain informed consent from potential volunteers.
• Document all communications with sponsor, labs, IRB, and other regulatory bodies.
• Maintain organized, accurate study records.
• Assist PI in conducting studies to ensure data integrity and subject safety.
• Enter data as required for protocol (paper-electronic data capture).
• Report and track adverse events as defined by each protocol.
• Perform study close-out procedures and store records appropriately.
• This role may include additional duties as needed by ERG.

Skills

Communication skills

GCP/ICH knowledge

Regulatory knowledge

Data entry

Independent decision making

Education

High School Diploma

College degree

Tools

Study Manager

Job description

Evolution Research Group (ERG) is a neuroscience-focused clinical development company providing Phase I–IV trial execution in the U.S. and globally.

The Clinical Research Coordinator will coordinate trials, ensure regulatory compliance, and manage subject enrollment under the PI and Site Director, while maintaining accurate documentation per FDA, GCP, and SOPs. The role requires understanding protocol requirements, informed consent, data capture, and ongoing communication with sponsors, IRBs,