Clinical Research Coordinator in Los Angeles, CA for UCLA

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Assistant / Associate Professor of Instruction Clinical Laboratory Services

The University of Texas Medical Branch

Galveston, Texas

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Care Technician, Patient Care Unit

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Vail, Colorado

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Denver, Colorado

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Vanderbilt Health

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University of Maryland Medical System

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Medical Lab Scientist MLS/MLT

AdventHealth

Killeen, Texas

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Section Lab Supervisor - Chemistry - Day Shift - Rotating Weekends

Northeast Georgia Health System

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Nuclear Med Tech PRN

Baylor Scott & White Health

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Emergency Room Patient Care Tech-FT

BJC HealthCare

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MT/MLS II - Microbiology, Days

BJC HealthCare

Saint Louis, Missouri

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OurLegacy Clinical Donation Associate

AdventHealth

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MT/MLS II

BJC HealthCare

Saint Louis, Missouri

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Data Analyst Flow Cytometry

Labcorp

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MT/MLS (Non-Reg) - Customer Service

BJC HealthCare

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Chief Pilot - Life Lion

Penn State Health

Hershey, Pennsylvania

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Emergency Room Patient Care Tech-FT

BJC HealthCare

Belleville, Illinois

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Medical Technician

Veterans Affairs, Veterans Health Administration

Castle Rock, Colorado

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MT/MLS II - Core Lab

BJC HealthCare

Saint Louis, Missouri

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Certified Medical Lab Tech - Night Shift

Northeast Georgia Health System

Gainesville, Georgia

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Certified Medical Assistant OBGYN

AdventHealth

Port Charlotte, Florida

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EMT-B

Denver Health

Denver, Colorado

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MedTech NO Nights or Weekends Plus Sign-On

Labcorp

Buffalo, New York

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WakeMed Travel Cardiovascular Specialist-$80/hr.

WakeMed Health & Hospitals

Raleigh, North Carolina

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MT/MLS II - Evenings

BJC HealthCare

Saint Louis, Missouri

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Clinical Research Coordinator

Baylor Scott & White Health

Plano, Texas

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Clinical Research Coordinator

DescriptionJoin our team as a Clinical Research Coordinator/Manager in the Division of Dermatology, working under the guidance of the Principal Investigator (PI). You’ll manage and coordinate clinical research trials, from recruiting and screening participants to collecting data and ensuring the trials run smoothly. Your key tasks will include: Recruiting and assessing potential study participants.Building and maintaining strong relationships with participants to encourage their ongoing involvement.Keeping participant information confidential.Collecting data and documenting consent and any adverse events.Collaborating with the CTSI comput

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