Clinical Research Coordinator

MFSTalent
Palo Alto, CA, United States
$32-$34 an hour
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
  • 2 days ago
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