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Coordinator
WMCHealth

Margaretville, New York

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Clinical Research Nurse II
Nemours

Orlando, Florida

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Lab Assistant
Labcorp

Burlington, North Carolina

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Physician - Chief Hematology/Oncology
Veterans Affairs, Veterans Health Administration

Biloxi, Mississippi, Mississippi

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VP Business Operations FL Institute Cardiovascular Medicine
Nemours

Orlando, Florida

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Physician - Interventional Cardiologist
Marshfield Clinic Health System

Marshfield, Wisconsin

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Phlebotomist Float
Labcorp

Washington,

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Specimen Accessioner
Labcorp

Colorado Springs, Colorado

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Phlebotomist Float
Labcorp

Richmond, Virginia

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Retail Pharmacy Technician
Baylor Scott & White Health

Round Rock, Texas

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Laboratory Assistant
Sonic Healthcare USA

Woodbury, New York

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RN, Registered Nurse - Day Surgery
CHRISTUS Health

Tyler, Texas

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RN, Registered Nurse - NICU
CHRISTUS Health

Tyler, Texas

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Senior Research Administrator
UCLA

Los Angeles, California

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Research Coordinator (Limited)
UCLA

Los Angeles, California

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Phlebotomy Floater Part - time
Sonic Healthcare USA

Memphis, Tennessee

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Speech Language Pathologist - Head & Neck
Fred Hutchinson Cancer Center

Seattle, Washington

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Phlebotomist Floater
Labcorp

Lindenhurst, Illinois

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Staff Research Associate II
UCLA

Los Angeles, California

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Laboratory Assistant I - OBGYN (Limited)
UCLA

Los Angeles, California

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Pediatric Psychologist
Akron Children's - Physician Recruitment

Akron, Ohio

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Primary Care Physician -Springfield Medical Director
Veterans Affairs, Veterans Health Administration

Springfield, Illinois, Illinois

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Patient Services Specialist
Baylor Scott & White Health

Killeen, Texas

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TTUHSC Pediatric Hematology/Oncology in West Texas! Ranked as a Best City to raise a family!
Texas Tech University Health Sciences Center

Lubbock, Texas

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Phlebotomist Floater
Labcorp

Libertyville, Illinois

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Clinical Research Coordinator II (Hybrid)
Job DescriptionThe Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries.Responsible for compiling and reporting on each study including information related to protocol activity, accrual


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