Location
SAINT LOUIS, MO 63110
Scheduled Hours
40
Position Summary
Under the direction of a Research Coordinator or Principal Investigator (PI), supports clinical research activities, including screening, consenting, and enrolling study participants. Assists with the collection, documentation, management, and reporting of clinical research data in accordance with study protocols and applicable regulatory requirements.
Job Description
Primary Duties & Responsibilities:
Participant Recruitment, Screening, and Consent:
Assists with the recruitment and screening of potential study participants in accordance with study protocols.
Reviews medical records and other relevant information to assess preliminary eligibility for participation.
Explains study procedures and requirements to participants and their caregivers or legally authorized representatives, as applicable.
Obtains informed consent in accordance with approved protocols and institutional requirements.
Study Visit Coordination and Participant Support:
Schedules study visits and follow-up appointments and coordinates required study procedures.
Prepares study packets, questionnaires, and other materials needed for participant visits.
Assists with study visits by escorting participants to designated areas and coordinating their movement through various visit procedures.
Explains and coordinates laboratory testing, diagnostic procedures and other study-related activities.
Provides participants and caregivers with study-related information and directs them to appropriate resources as needed.
Data Collection and Documentation:
Collects and records research data from participant interviews, questionnaires, medical records, diagnostic tests, and other approved sources.
Completes study forms, source documentation, and other required paperwork in accordance with study protocols and regulatory requirements.
Performs basic, protocol-defined assessments and assists with the review of collected data for completeness and accuracy.
Prepares and maintains study documentation and reports as required.
Laboratory and Clinical Research Support:
Assists with the collection, processing, labeling, storage and preparation of blood and other biological specimens for research purposes, as trained and authorized.
Coordinates laboratory testing and other diagnostic procedures required by study protocols.
Maintains study supplies an ensures that necessary materials are available for participant visits and research activities.
General Research Support:
Works collaboratively with Research Coordinators, PIs and other research team members to support study activities.
Performs other duties as assigned to support the successful conduct of clinical research studies.
Working Conditions:
Job Location/Working Conditions:
Normal office environment
Physical Effort:
Typically sitting at a desk or table
Equipment:
Office equipment
The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time.
Required Qualifications
Education:
High school diploma or equivalent high school certification or combination of education and/or experience.
Certifications /Professional Licenses :
No specific certification/professional license is required for this position.
Work Experience:
Customer Service (1 Year)
Skills:
Not Applicable
Driver's License:
A driver's license is not required for this position.
More About This Job
WashU seeks highly motivated individuals who are able to perform duties in a manner consistent with our core mission and guiding principles.
Preferred Qualifications
Education:
No additional education unless stated elsewhere in the job posting.
Certifications /Professional Licenses :
No additional certification/professional licenses unless stated elsewhere in…