knownwell
Healthcare
ClinicalResearchCoordinator
“Clinical Research Coordinator at knownwell. Skills: Clinical trial coordination, Regulatory compliance, Patient safety, Data management. Coordinate and manage clinical trials. Oversee patient recruitment and enrollment”
Industry & Context.
What They're Looking For.
Must Have
Bachelor's degree in a related field, 3+ years of experience in clinical research, GCP Certification, BLS Certification, IATA Certification, CSSR Certification
Nice to Have
CCRC Certification, Master's degree, 2+ years of experience with independent trial management, Experience with Florence, Experience with Advarra, Experience with Greenphire
What You'll Do.
Coordinate and manage clinical trials
Oversee patient recruitment and enrollment
Schedule and oversee patient visits
Maintain study documentation
Report adverse events
Manage study drug and sample handling
Generate invoices for sponsors
How You'll Work.
Team & Collaboration
Act as liaison between research team, patients, and stakeholders; Collaborate with trial site staff, sponsor or CRO; Work closely with Principal Investigator; Communicate with sponsor representatives
Communication Scope
Excellent written and verbal communication skills
Process & Methodology
Oversee site initiation, monitoring, closeout activities, Manage study documentation, Ensure timely completion of monitoring follow-up
Applying for this Clinical Research Coordinator role?
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