Research & Development Institute, Inc.
  • Los Angeles, CA, USA
  • Competitive
  • Salary
  • Full Time

Competitive


Job Description

This is an opportunity for an experienced Senior Clinical Research Coordinator to contribute to medical research as part of one of the largest HIV related trials in history. The ideal candidate understands the importance of the clinical research process and has experience in all the responsibilities of a research coordination (consenting, phlebotomy, labs, EDC, and sponsor monitoring visits.

For the right motivated candidate, this is an excellent opportunity to contribute and grow with our company.

Duties:

  • Adhere to Research SOP's
  • Comply with Good Clinical Practices and the study protocols
  • Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
  • Discuss study protocols with patients and verify the informed consent documentation
  • Meet with a patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study
  • Dispense study medication in a professional and accountable manner following protocol requirements
  • Collect, process, and ship blood/urine specimens at scheduled patient visits
  • Perform ECGs and obtain vital signs of patients
  • Schedule all patient research visits and procedures consistent with protocol requirements
  • Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy
  • Maintain accurate and complete regulatory files
  • Prepare for monitor visits
  • Administer questionnaires/diaries per protocol

Requirements and Qualifications:

  • Minimum four years of experience on-site as a research coordinator in pharma or device clinical trials.  
  • Venipuncture / EKG experience
  • Excellent written and verbal communication skills

Nice to have

  • ACRP or SOCRA Certification

 

Research & Development Institute, Inc.
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