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Cancer Clinical Research Coordinator Associate - Hematology
Company | Stanford University School of Medicine |
Address | Stanford, CA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Higher Education |
Expires | 2023-07-11 |
Posted at | 11 months ago |
Job ID 99220 Date posted 06/09/2023
- Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.
- Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out.
- 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.
- Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
- Participate in monitor visits and regulatory audits.
- 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.
- Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
- Coordinate collection of study specimens and processing.
- Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
- Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
- Strong oral and written communication skills
- Familiarity with IRB guidelines and regulations
- Previous experience with clinical research.
- Excellent attention to detail
- Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
- Proficiency in using computers, software, and web-based applications in a previous administrative setting
- Knowledge of the principles of clinical research and federal regulations.
- Proficiency with Microsoft Office.
- Knowledge of medical terminology.
- Strong interpersonal skills.
- 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.
- 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.
- Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
- 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.
- Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
- Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu .
- Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
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