Research Coordinator

Pay Rate: $25/hr

***Minimum of one year of experience in a addiction/substance abuse and research environment***

Summary

The Research Coordinator is responsible for managing complex protocols evaluating investigational drugs, devices or other research interventions. Directs and supports the conduct of clinical studies, acting as a liaison between investigator, institutional review board and sponsor, to ensure adherence to the research protocol throughout cycle of study. As well as maintaining required documents and training for each research protocol.

Responsibilities:

The Research Coordinator will assist in conducting study visits and execute all aspects of the study protocol, including, but not limited to:

• Strict adherence to study protocol; obtain exemptions when necessary/appropriate
• Prepares study participant source visit documentation at each visit.
• Assist with filling out study participant visit information into source documents.
• Assist with filing of lab requisitions, study specific documentation and other study participant information into their proper location.
• Coordinates study visit schedules for inpatient and outpatient study participants with the nursing staff.
• Maintain and track accurate records of the receipt of study drug and materials.
• Perform clinical task including, but not limited to; vital signs, height & weight, EKG, Phlebotomy, specimen packaging
• Obtain and ship study participant blood samples and other specimens for laboratory analysis as described in study protocol.
• Collect pertinent information and data from study participant charts and records, subject interviews, and other sources.
• Review eCRF/CRFs, source documentation, and study files to ensure completeness.
• Assist with entering study visit source into eCRF/CRF in a timely manner and according to site standard operating procedures.
• Maintain and keep up to date the daily temperature logs.
• Provide training and direction to assistants or new personnel on protocol procedures.
• Assist with purchasing/maintaining inventory for patient retention items and laboratory equipment.

Requirements:

• Level II Background clearance
• Acceptable Motor Vehicle Registration driver's license record in accordance with the underwriting guidelines set by Aspire's insurance company as described in the AHP Corporate Transportation Policy 3.9.1
• High School Diploma or GED
• RN or LPN License preferred
• Minimum of one year of experience in a mental health and research environment
• Proven experience in research coordination or clinical trials management.
• Strong understanding of HIPAA regulations and patient confidentiality requirements
• Familiarity with statistical software for data analysis is a plus.
• Excellent organizational skills with the ability to manage multiple projects simultaneously

If you are passionate about advancing behavioral health through research and want to make a meaningful impact, we invite you to apply for the Research Coordinator position at Aspire Health Partners today!