Associate Clinical Research Coordinator - Great Hospital - $35.00 Hr.

Job Summary:
Receives direction from principal investigator, supervisor, or other staff involved in research protocol(s). Interacts with various departments within the institution. Works cooperatively with other investigators and personnel at all levels. Interacts with research participants, other research centers, and sponsoring companies to resolve problems and ensure efficient completion of research studies.

Job Responsibilities:
-Coordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
-May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with direction but does not have overall responsibility for these studies.
-Screens, enrolls, and recruits research participants.
-Coordinates schedules and monitors research activities and subject participation.
-Recognizes adverse events, protocol deviations, and other unanticipated problems and reports appropriately. Collects, abstracts, and enters research data.
-Performs administrative and regulatory duties related to the study as assigned.
-Some travel may be required.
-ADDENDUM (if applicable) Protocol Development and Maintenance Activities Responsibilities may include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (i.e. data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; Institutional Review Board (IRB) submission; and communication with study sites and/or federal agencies regarding study status changes.
-Participates in other protocol development activities and executes other assignments as warranted and assigned.

Skills:

Required Skills & Experience:
-See Education Section for Required Experience.

Preferred Skills & Experience:
-One (1) year of clinical research experience.
-Medical terminology course.

Education:

Required Education:
-HS Diploma with at least three (3) years of experience.
OR
-Associate's degree/college Diploma/Certificate Program with at least one (1) year of experience, Associate’s in Clinical Research from an accredited academic institution without experience.
OR
-Bachelor's degree and experience should be in the clinical setting or related experience.

Pay: $35.00 per hour

Work Location: In person

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Associate Clinical Research Coordinator - Experience Required - $35.00 Hr.