Clinical Research Coordinator, CRC

Hawthorne Health

. Conduct and coordinate all aspects of clinical trial activities at the site .

Posted 10/6/2026full-timeGadsden • Alabama • United StatesJunior💰 $25 - $35 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in conducting clinical trial activities, including patient recruitment, data management, and regulatory compliance. Proficient in phlebotomy and electronic data capture systems, ensuring adherence to clinical protocols and guidelines.

Highest-signal resume keywords

Clinical Trial OperationsPhlebotomy CertificationData ManagementGCP ComplianceElectronic Data Capture Systems

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

PhlebotomyData EntryRegulatory DocumentationClinical Trial CoordinationBiological Sample Processing

Soft Skills

Attention to DetailOrganizationTime ManagementInterpersonal CommunicationTeam Collaboration

Tools & Technologies

Microsoft OfficeElectronic Data Capture Systems

Certifications & Qualifications

Phlebotomy CertificationCPR Certification

Industry Keywords

GCPICHFDAIRBInformed Consent

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Conduct and coordinate all aspects of clinical trial activities at the site
Perform phlebotomy on patients following proper clinical and safety protocols
Recruit, screen, and enroll study participants according to inclusion/exclusion criteria
Schedule and conduct study visits while ensuring adherence to protocol requirements
Collect, process, and ship biological samples according to study-specific guidelines
Complete and maintain source documents, regulatory binders, and informed consent forms
Perform timely and accurate data entry into electronic data capture systems
Communicate with sponsors, monitors, and other research team members
Ensure compliance with GCP, ICH, FDA, and IRB regulations
Assist with monitoring visits and audit preparation

Requirements

What you’ll need

Minimum of 1–2 years of experience as a Clinical Research Coordinator, in a similar environment
Phlebotomy certification preferred OR demonstrated competency in venipuncture (pediatric and adult required)
Strong understanding of clinical trial operations, regulatory documentation, and data management
Excellent attention to detail, organization, and time management skills
Strong interpersonal and communication abilities with patients and clinical staff
Proficient in Microsoft Office and electronic data capture systems
CPR certification preferred

Benefits

Comp & perks

Flexible mix of remote and on-site responsibilities
Flexible work schedule averaging approximately 32–40 hours per week
Support from an experienced centralized operations team
Leadership and ownership opportunities at the site level