Clinical Research Coordinator

ClinicalResearchCoordinator

Columbus, Ohio, United States FULL TIME
The Brief

“Clinical Research Coordinator at Clinical Research Coordinator. Skills: Clinical research, Data management, Subject recruitment. Recruit, consent and enroll subjects. Manage study data and subject information”

Industry & Context.

Problems you'll solve

Demonstrated analytical skills

Eligibility Requirements

May require evening and weekend hours, Physical Requirements: OCCASIONALLY: Cold Temperatures, Fume /Gases /Vapors, Loud Noises, Reaching above shoulder, Squat/kneel FREQUENTLY: Bend/twist, Biohazard waste, Blood and/or Bodily Fluids, Chemicals/Medications, Communicable Diseases and/or Pathogens, Lifting / Carrying: 0-10 lbs, Lifting / Carrying: 11-20 lbs, Lifting / Carrying: 21-40 lbs, Machinery, Patient Equipment, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 26-40 lbs, Pushing / Pulling: 41-60 lbs, Pushing / Pulling: 61-100 lbs, Sitting, Standing, Walking CONTINUOUSLY: Audible speech, Computer skills, Decision Making, Depth perception, Flexing/extending of neck, Hand use: grasping, gripping, turning, Hearing acuity, Interpreting Data, Peripheral vision, Problem solving, Repetitive hand/arm use, Seeing – Far/near

What They're Looking For.

Must Have

Associates degree, STNA, PCA, LPN, MA or equivalent work-related experience required

Nice to Have

BAS preferred, Understanding of medical terminology and clinical research preferred, Previous experience in clinical research or health care related field preferred

What You'll Do.

consent and enroll subjects

Manage study data and subject information

Prepare and process human specimens

Complete screening sheets and recruitment logs

Create source documents for data collection

Schedule subject study visits

Adhere to quality control guidelines

Complete Case Report Forms (CRFs)

Maintain regulatory binder and documents

How You'll Work.

Team & Collaboration

Collaborates, coordinates, and schedules subject study visits with other hospital services and the PI/sub-I

Communication Scope

Excellent verbal and written communication skills

Process & Methodology

Manages elements of a clinical study

Free ATS check

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