Clinical Research Coordinator Associate, Pediatric Hematology
Clinical Research Coordinator Associate, Pediatric Hematology🔍School of Medicine, Stanford, California, United States📁Research📅Nov 18, 2020 Post Date📅87845 Requisition #Clinical Research Coordinator Associate, Pediatric HematologyThe Stanford Cancer Institute (SCI) is one of an elite number of National Cancer Institute-Designated Comprehensive Cancer Centers in the country, and is a prominent, dynamic, growing and complex Institute within the Stanford University School of Medicine. The SCI actively works to build synergies and collaborations among faculty with cancer-relevant expertise from four Schools and over 30 departments across Stanford University. We seek a Clinical Research Coordinator Associate to help us enact our mission to reduce cancer mortality through comprehensive programs of cancer research, treatment, education and outreach. Given the SCI’s mission, breadth, and depth, it employs over 320 staff members in a fast-paced, team-oriented, and forward-thinking environment with tremendous opportunities for personal and professional growth. The Cancer Clinical Trials Office (CCTO) is an integral component of the Stanford Cancer Institute since the vital work performed there enables our adult and pediatric cancer centers to translate research from the laboratory into the clinical setting. You will be working with an unparalleled leading edge community of faculty and staff who are fundamentally changing the world of health care in the cancer arena. Reporting to Clinical Research Manager, the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to support clinical research studies in Pediatric Hematology. We are seeking candidates with excellent organizational skills, attention to details and willingness to learn. Our staff run toward challenges, and you will have a demonstrated history of doing the same with a high degree of professionalism, initiative and flexibility. Responsibilities include working with the research team and clinical staff to help support study participant enrollment, consent process, study procedure completion, regulatory compliance and general communication. Core duties include: *Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out.*Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.*Coordinate collection of study specimens and processing.*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.*Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.*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.*Participate in monitor visits and regulatory audits.*Participate in CCTO learning activities (orientation classes, Education meetings and staff meetings) along with other pediatric research meetings, weekly research staff meeting and other relevant meetings assigned. DESIRED QUALIFICATIONS:
- Previous experience in working in clinical research.
- Previous experience in working in Hematology, Oncology, or Pediatrics.
- Strong interpersonal and communication skills.
- Proficiency with Microsoft Office.
- Knowledge of medical terminology.
- Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
- 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.
- 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.
- Occasional evening and weekend hours.
- Will be expected to participate in on-call schedule (1 week per month)
- Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
- 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.
- 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.
- Schedule: Full-time
- Job Code: 4924
- Employee Status: Regular
- Grade: F
- Department URL: http://cancer.stanford.edu/
- Requisition ID: 87845