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Job #2199  

Clinical Research Coordinator 

(Job #2199) RESEARCH COORDINATOR WITH BLOOD DRAW SKILLS needed Santa Monica Medical Practice.

ABOUT THE POSITION

  • Coordinate all aspects of clinical trial including recruiting, registration, taking vitals and blood draw, documenting and reporting results.
  • REQUIRES CRC CERTIFICATION
  • Must have experience in FDA Clinical Trials!!!
  • Must have venipuncture skills

REQUIREMENTS

  • Must have previous experience in healthcare clinical research and FDA Clinical Trials!
  • Have strong knowledge of regulatory paperwork and guidelines
  • Previous experience coordinating a clinical trial including all regulatory paperwork, scheduling, reports and overall ensure the clinical trials are run properly
  • Strong computer skills are required including fast and accurate typing,
  • Strong attention to details to schedule and document all the tests and results, chart reviews, reports, forms, manage budgets and contracts
  • Warm personality with an ability to help people to feel comfortable with their testing.
  • Ability to work independently with strong time-management skills.

SCHEDULE and COMPENSATION

  • Schedule is full-time, 5 days/week
  • Competitive salary based on experience: $25+
  • Benefits include 100% paid health insurance after 3 months, with Dental & Vision, 2 weeks accrued vacation after 1 year, paid holidays and sick days, Pension after 1 year with 5% match, and Paid Parking.

Apply for Job #2199

Job # 2192

Clinical Research Coordinator

(Job #2192) CRC - Clinical Research Coordinator to work at a medical practice near LAX!

ABOUT THE POSITION

  • An individual who, under the direction and ongoing supervision of the Principal Investigator, aids in the daily function of clinical research programs being performed.
  • Handles Phases 2 and 3 of Clinical trials so this experience is required
  • Administer questionnaires/diaries per protocol
  • Ensure that non-serious and serious adverse events are properly documented and reported
  • Ensure the filing and maintenance of all regulatory documents
  • Manage all required study startup documentation, training, and timelines on assigned study protocols
  • This position is fully in-office (no remote option)

QUALIFICATIONS AND SKILLS (May include, but are not limited to):

  • Minimum 2 years of experience
  • Previous experience with clinical trials REQUIRED
  • Comprehensive knowledge of FDA, GCP, CRF ICH guidelines, IRB and HIPAA as applied to clinical research.
  • Familiar with data entry platforms
  • Bilingual (English/Spanish) (Preferred not required)

SCHEDULE, SALARY AND BENEFITS

  • M-F 8a-5p
  • Pay: $22.00 - $31.00 per hour DOE
  • Health, vision, dental, paid holidays, Paid time off

Apply for Job #2192

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