Care Access
Healthcare
ClinicalResearchCoordinator
“Clinical Research Coordinator at Care Access. Skills: Good Clinical Practices, Protocol compliance, Patient monitoring. Screen study subjects. Enroll study subjects”
Industry & Context.
Problem solver; Critical thinker
Onsite work 5 days, Up to 10% travel, Lifting up to 25 lbs, Walking, Standing, Sitting, Driving
What They're Looking For.
Must Have
1-year prior Clinical Research Coordinator experience, Recent phlebotomy experience, National phlebotomy certification
Nice to Have
Bachelor's Degree preferred, Epic certification preferred
What You'll Do.
Screen study subjects
Enroll study subjects
Monitor study subjects
Ensure protocol compliance
Ensure regulatory compliance
Obtain informed consent
Complete documentation accurately
Follow patient privacy protocols
Follow patient safety protocols
Complete visit procedures
Complete basic clinical procedures
Review laboratory results
Alert value notification
Ensure investigator review
Discuss study medication
Discuss required procedures
Discuss eligibility criteria
Discuss impact on office flow
Prioritize activities
Maintain adherence to FDA regulations
Maintain adherence to ICH guidelines
Coordinate pre-study visits
Coordinate site initiation visits
Coordinate monitor visits
Identify adverse events
Identify Serious Adverse Events
Notify Principal Investigator
Enter data in real time
Record study medication inventory
Record medication dispensation
Record patient compliance
Resolve data management queries
Assist regulatory personnel
Assist with filing regulatory documents
Assist in creation of source documents
Assist in review of source documents
Assist with recruitment materials
Assist in development of recruitment plan
Obtain listing of potential candidates
Assess protocol amendments
Ensure training requirements met
Ensure study requirements met
Communicate clearly verbally
Communicate clearly in writing
Attend Investigator meetings
Ensure adequate supplies arrived
Interact professionally with patients
Interact professionally with sponsor representatives
Interact professionally with investigators
Interact professionally with personnel
Maintain effective relationships with participants
Maintain effective relationships with personnel
How You'll Work.
Team & Collaboration
Work with diverse team; Work with site staff; Work with Sponsor/CRO; Work with recruitment team; Work with clinical staff; Work with management
Communication Scope
Verbal communication; Written communication; Professional communication
Process & Methodology
Prioritization, Organization
Applying for this Clinical Research Coordinator role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Greenhouse
- Create a Greenhouse profile before applying — it saves time across multiple applications.
- Upload your resume as a PDF; the parser handles it better than Word.
- Answer all knockout questions carefully — wrong answers auto-reject before a human sees you.
- Enable email notifications to track application status in real time.
ANONYMOUS · UNFILTERED
What do employees actually say about Care Access?
Real rants from real employees. Read before you apply.