The Clinical Research Coordinator I - supports the coordination and conduct of clinical research studies under the guidance of senior team members. This role assists with participant screening and eligibility determination, data collection, recruitment, scheduling, and follow-up while ensuring all activities are performed in compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The coordinator contributes to all phases of the study, from start-up through close-out, and provides general protocol support to the research team.

Duties:
May assist in compiling
Editing
Proofing written reports for both internal and external administrative offices.
May perform data analysis using a variety of software packages.
Performs other duties as assigned.

Preferred Skills:
Ability to operate various office machines including printers, computers and various software packages
Interpersonal skills Knowledge of Microsoft Office products
Written and verbal communication skills Data entry skills
Time Management Organizational Skills
Problem solving and adaptability
Experience working/talking with clinical populations

20 hours a week.

High School Diploma Field of Study - Psychology, Biology Health Services Type of Experience - Clinical Comparable Work experience can substitute for minimum

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