Clinical Research Coordinator

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 dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.

Why join us?

We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.

Job Description:

The Clinical Research Coordinator is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC completes all study related procedures and distributes study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. They maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

Responsibilities:

General

• Obtaindetailed knowledge of all components of each study protocol through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study.
• Assist to develop draft source documents and review the documents for accuracy and clarity prior to study start up.
• Reviewwith Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study.
• Managestudies with direct oversight from Site Director, and Principal Investigator to ensure compliance with protocol requirements.
• Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
• Contribute to the SOP review and development as delegated by the Site Director.

Study Management

• Perform study activities as delegated by the Principal Investigator and under the supervision of the Site Director.
• Attend the investigator meeting for each assigned protocol, as appropriate with directive from Site Director.
• In conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required.
• Screen, enroll subjects and schedule subject visits in conjunction with Principal Investigator
• Review and obtain informed consent from with potential study volunteer
• Document all written and phone correspondences with sponsor, labs, IRB other regulatory organizations
• Maintain organized, accurate and complete study records
• Assist Principal Investigator in conducting studies in manner to ensure integrity of data and safety of subjects.
• Enter data as appropriate for protocol (paper-electronic data capture)
• In conjunction with Principal Investigator, accurately report and track adverse events as defined by each study protocol.
• Perform study close-out procedures.
• Store study records appropriately
• Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.

Skills and Qualifications:

• Education and experience
  • High School Diploma or its 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.
  • Demonstratethe initiative to act independently, initiate activity as required and make appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy.
  • Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.
• Requirements
  • Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
  • Excellent communication skills (interpersonal, written, verbal)
  • Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)