Clinical Research Coordinator

Equivalent Experience
Clinical Research Coordinator position within a large hospital group in Southern California.

Clinical Research Coordinator will support a research portfolio of 400+ sponsor-initiated clinical trials across multiple therapeutic areas, including: infectious disease, oncology/hematology, neurology, diabetes, radiology, ophthalmology.
Job Duties:
Responsible for reviewing and comprehending research protocols.
Assist in recruiting potential subjects.

Schedule patients within inclusion criteria.
Phone screen patients.
Assist during patient visits.
Coordinates day to day activities of several small scale project(s) or phases of one or more larger projects.

Collects project data through interviews, chart review or other methods.
May collect, secure and assist with biospecimen management.
May assist in development of study tools (e.g.

tracking forms, questionnaires, chart review forms, etc.).
Responsible for data collection and data management inputting into appropriate EDC.
If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites.
Adheres to compliance and privacy/ confidentiality requirements and standards.

Adheres to GCP and compliance regulations for clinical trials.
Assists with and/ or oversees quality assurance of study activities; ensures quality data.
May interface with IRB and/ or draft portions of IRB protocols, amendments, continuing reviews, etc.
May contribute to portions of study presentations.
Reviews scientific literature and synthesizes and summarizes information.
Qualifications:
2+years of relevant clinical research experience
Bachelor’s degree preferred
ACRP/CCRC certifications preferred
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