Clinical Research Coordinator, Part-Time Contract
Overview
Own in-field participant recruitment and study coordination for a balance impairment trial at a Falls Church area site. You will screen, consent, schedule visits, and ensure data integrity across EDC systems in a clinical research setting. This role emphasizes meticulous documentation, regulatory compliance, and participant engagement within a contract arrangement.
What You'll Do10
- 1Build participant outreach to identify eligible candidates and prescreen for eligibility
- 2Design and conduct phone screenings and review inclusion exclusion criteria
- 3Obtain informed consent following regulatory and ethical standards
- 4Prepare for study visits including scheduling and document preparation
- 5Coordinate participant follow ups to sustain retention and protocol adherence
- 6Schedule in person visits and send reminders and information as needed
- 7Enter study data into electronic data capture systems with accuracy
- 8Create and maintain source documents and ensure audit ready records
- 9Resolve EDC data queries promptly
- 10Maintain and organize study binders in compliance with regulatory requirements
Requirements5
- 12+ years of experience as a Clinical Research Coordinator
- 22+ years of patient recruitment experience
- 32+ years of experience with Electronic Medical Records EMR
- 4Training in HIPAA and Good Clinical Practice GCP
- 5Previous experience in clinical trials and patient pre screening
Salary Insight
$25 - $33k per year
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
Actalent
VerifiedClinical Research Coordinator, Regulatory Compliance & Data Integrity
You will own the full lifecycle of clinical research studies, from IRB submissions to data audits, across 3+ concurrent protocols at a major academic medical center. You act as the central hub between principal investigators, sponsors, and IRB committees, ensuring each trial meets regulatory and institutional standards. You will drive study compliance, manage participant consent, and safeguard data integrity through systematic quality checks. This role offers direct exposure to FDA-regulated environments and a fast track to CCRC certification.
CENTER FOR DERMATOLOGY
VerifiedClinical Research Coordinator Center for Dermatology
We seek a motivated Clinical Research Coordinator to lead clinical trials at CENTER FOR DERMATOLOGY in Washington DC and Annapolis MD. You will oversee trial planning execution and data collection ensuring regulatory compliance and high-quality data. Your expertise will advance medical research and improve patient outcomes. This role offers leadership in a fast-paced collaborative environment.
Actalent
VerifiedSr Clinical Research Coordinator Oncology
Lead senior clinical research coordinator overseeing study execution for diverse portfolio of investigator initiated and industry sponsored trials. Seeking proactive research professional passionate about clinical research patient care and driving innovative therapies.
DocTrials
VerifiedClinical Research Coordinator - DocTrials
Coordinate patient visits and lead interventional protocols at multiple Phoenix Valley offices. Manage patient acquisition and enrollment through community outreach while ensuring strict adherence to FDA and ICH-GCP guidelines. Consolidate study data and communicate updates via Basecamp.
System One
VerifiedClinical Research Coordinator, Regulatory Compliance
As a Clinical Research Coordinator, you will own the execution of clinical protocols at our Inglewood site, supporting 5+ active studies with a focus on participant safety and data integrity. You'll work directly with the Principal Investigator and senior research staff, collaborating with cross-functional teams including data management and regulatory affairs. This contract role stands out for its hands-on involvement in the full study lifecycle, from screening to closeout, in a fast-paced research environment.
CenExel Clinical Research
VerifiedClinical Research Coordinator, Phase I-IV Trials
Coordinate Phase I-IV clinical trials with strict adherence to ICH and GCP guidelines at CenExel Clinical Research. Manage patient involvement from study initiation through completion across diverse therapeutic areas like Psychiatry, Dermatology, and Neurology. Work onsite in Los Angeles with a dedicated team of research professionals and a collaborative environment that prioritizes quality and work-life balance. This role includes direct patient interaction, data management, and regulatory duties, offering a chance to impact clinical research quality.