Clinical Research Coordinator Assistant

at  Stanford University

Stanford, California, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate19 Feb, 2025USD 32 Hourly20 Nov, 20241 year(s) or aboveTwist,Medical Terminology,Grasp,TrainingNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

The Adult Brain Tumor Center in the Department of Neurosurgery is seeking an Assistant Clinical Research Coordinator to perform administrative support duties related to clinical research. The candidate will work under the direct supervision of the principal investigator at Stanford University and Stanford Hospital and Clinics.

EDUCATION & EXPERIENCE (REQUIRED):

Two-year college degree and one year of relevant experience or an equivalent combination of experience, education, and training.

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

General knowledge of medical terminology.

PHYSICAL REQUIREMENTS*:

  • Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
  • Occasionally sit, reach above shoulders, perform desk-based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
  • Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.

    • Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.

    Responsibilities:

    • Schedule and/or call subjects for appointments; contact participants with reminders or other requirements.
    • Prepare, distribute, and process questionnaires.
    • Perform clerical duties in the preparation of regulatory documents. Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence.
    • Collect study specimens according to protocol.
    • Prepare, process, and ship specimens/samples accurately under well-defined requirements.
    • Order and maintain equipment and supplies.

      • Other duties may also be assigned.


      REQUIREMENT SUMMARY

      Min:1.0Max:6.0 year(s)

      Hospital/Health Care

      Pharma / Biotech / Healthcare / Medical / R&D

      Health Care

      Graduate

      Proficient

      1

      Stanford, CA, USA