Clinical Research Coordinator II - Neurology
Washington University in St. LouisAbout the role
Scheduled Hours
40Position Summary
The Clinical Research Coordinator II will directly interact with family/primary caregivers, participants, and an inter-disciplinary team in a research setting. Position assists the Knight ADRC Clinical Trials Unit‐(KACTU) team with coordination of all aspects of clinical research for fast-paced and complex multi-site clinical trials, and may be responsible for multiple research studies simultaneously. This position will coordinate study procedures to provide to eligible participants, consistent with study procedures and techniques and verified documentation. This position includes extensive interaction with diverse participants, study sponsors, research staff, and investigator.Consistent with its academic mission and standards, the Washington University School of Medicine is
committed to achieving excellence through diversity, inclusion, equity, and belonging. As a community of faculty, staff and students engaged in research, patient care, scholarship, teaching and learning, the
School of Medicine fosters an environment that is diverse, inclusive, humane, and welcoming. Efforts are made to provide a supportive environment in which people from a wide variety of diverse backgrounds and cultures may encounter each other in a spirit of cooperation, openness, and mutual respect.
Job Description
Primary Duties & Responsibilities:
Provides coordination of clinical trials, including assisting with startup, coordinating participant visits, conducting assessments, planning, imple‐mentation, and conduct of other study proce‐dures, assuring adherence to study protocols, completing study documentation and data en‐try, and assisting study physicians in study procedures.
Works with staff to identify, screen and enroll study subjects; ensures lab and data are obtained according to established protocol.
Trains and supervises staff assigned to work on the research project.
Coordinates handling of specimens, administration of clinical trials, collection of source information and case reporting.
Prepares/submits event reports in adherence with study procedures, budget and established guidelines.
Assists research associates from sponsoring organization, providing study explanations and reports as necessary.
Authorizes payments to ancillary organizations for services received and accounts for payments from organization serviced.
Working Conditions:
Job Location/Working Conditions
Normal office environment
Exposure to blood-borne pathogens
Requires protective devices
Patient care setting
Direct patient care setting
Physical Effort
Typically sitting at desk or table
Typically bending, crouching, stooping
Occasional lifting (25 lbs or less)
Equipment
Office equipment
Clinical/diagnostic equipment
Required Qualifications
Education:
Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
Certifications/Professional Licenses:
Work Experience:
Skills:
Driver's License:
More About This Job
Required Qualifications:
- Basic Life Support certification must be obtained within one month of hire date.
- Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirement).
Preferred Qualifications
Education:
No additional education unless stated elsewhere in the job posting.
Certifications/Professional Licenses:
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