Clinical Research Coordinator

4 weeks ago


Palo Alto, United States MFSTalent Full time
Job Description

  • Shift: Onsite, with occasional 1 day remote. 8 AM - 4:30 PM
  • Work location: Palo Alto, CA
  • Compensation: $32 to $34 per hour
Duties and Responsibilities
  • Serve as primary contact with research participants, sponsors, and regulatory agencies for research projects within our Lung Transplantation team.
  • Serve as primary contact with research participants, sponsors, and regulatory agencies for research projects within our Lung Transplantation team.
  • Determine eligibility of and gather consent from study participants according to protocol criteria.
  • Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
  • Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed.
  • Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
  • Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
  • Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
  • Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
Job Requirements

Education Qualifications
  • Two-year college degree and two years related work experience or a bachelor's degree in a related field or an equivalent combination of related education and relevant experience.
Experience
  • Desired qualifications include experience with interventional drug treatment trials, clinical experience with patients with pulmonary disease, and completion of a clinical trials certification program or related courses.
Benefits
  • Health/Dental/Vision Insurance
  • Sick time off


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