Clinical Research Coordinator

6AM City, LLC

False Pass (AK)

On-site

USD 39,000 - 41,000

Full time

10 days ago

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Benefits offered by this job

Medical

Dental

Vision

Telemedicine

Life insurance

Job summary

Kelly Science & Clinical is seeking a Clinical Research Coordinator for a contract role at a study site in West Chester, PA. The position offers a first-shift schedule from Monday to Friday with hourly compensation of $28–$30.

The CRC will support coordination and execution of clinical studies, ensure compliance with protocols and regulatory requirements, and work closely with PIs and participants to ensure accurate data collection and adherence to study procedures.

Qualifications

High school diploma or equivalent required; an associate’s degree or higher in a health-related field preferred.
Basic knowledge of clinical research strongly preferred.
Medical terminology & patient care experience required.
Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities.
Ability to communicate clearly and professionally with diverse populations.
Ability to work collaboratively in a fast-paced, team-oriented environment.
Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines strongly preferred.
Experience with participant screening and the informed consent process strongly preferred.
Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred.

Responsibilities

Coordinate and execute clinical research protocols under supervision of the PI and senior staff.
Conduct screening visits to collect medical history and other information from study participants.
Assist with informed consent and enrollment of study participants per protocol and ethical guidelines.
Schedule study visits, procedures, and follow-up activities with study participants and clinical teams.
Collect, record, and maintain accurate clinical research data and source documentation in compliance with standards.
Communicate with study participants to provide education and support adherence to requirements.
Monitor study progress and report adverse events and protocol deviations.
Adhere to SOPs and GCP guidelines.
Draw, process, and ship laboratory specimens if qualified.
Scan and file study records and maintain organized documentation.
Apply critical thinking to support efficient study operations and problem resolution.
Perform other duties as assigned.

Skills

Organizational skills

Communication skills

Team collaboration

Medical terminology

GCP knowledge

HIPAA knowledge

IATA guidelines

Electronic data capture

Clinical trial management software

Microsoft Office

Education

High school diploma

Associate degree in health-related field

Tools

Electronic data capture systems

Clinical trial management software

Microsoft Office

Job description

Job Description

Clinical Research Coordinator Kelly® Science & Clinical is seeking a Clinical Research Coordinator for contract position with a clinical leader at their study site in West Chester, PA. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Compensation: $28-30/hr

Schedule: Monday-Friday, 1st shift

Location: West Chester, PA

Duration: ASAP until 12/31/2026 (may extend or go perm)

Summary

The Clinical Research Coordinator (CRC) supports the coordination and execution of clinical research studies within a healthcare setting. This role ensures clinical trials are conducted in compliance with study protocols, regulatory requirements, and institutional policies while protecting participant safety and data integrity. Working closely with Principal Investigators (PIs), research staff, and study participants, the CRC assists with participant screening, data collection, and the coordination of study activities to ensure accuracy, efficiency, and high-quality research outcomes.

Responsibilities

Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff
Conduct screening visits to collect medical history & other information from study participants
Assist with informed consent and enrollment of study participants in accordance with protocol requirements and ethical guidelines
Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams
Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards
Communicate with study participants to provide education, answer questions, and support adherence to study requirements
Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team
Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines
Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in accordance with regulations (if qualified)
Scan, upload, file, and maintain organized study records and documentation
Apply critical thinking skills to support efficient study operations and problem resolution
Perform other duties as assigned

Qualifications

High school diploma or equivalent required; an associate’s degree or higher in a health-related field preferred
Basic knowledge of clinical research strongly preferred
Medical terminology & patient care experience required
Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities
Ability to communicate clearly and professionally with diverse populations
Ability to work collaboratively in a fast-paced, team-oriented environment
Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines strongly preferred
Experience with participant screening and the informed consent process strongly preferred
Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred

Certificates, Licenses, and Registrations

Medical Assistant (MA) certification preferred
Current CPR/BLS certification preferred
Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred

Benefits

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources.

medical
dental
vision
telemedicine
term life
whole life
accident insurance
critical illness
a legal plan
short-term disability
retirement savings plan
service bonus and holiday pay plans (earn up to eight paid holidays per benefit year)
transit spending account
paid sick leave under the applicable state or local plan