Job Description: The 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. Job Responsibilities: Ensure that all regulatory submissions for cooperative group study renewals and amendments are submitted to CTSU in a timely manner. Review and collect source documents enabling the completion of study documents/case report forms for clinical research projects using STSU website, OnCore, RedCap, iMedidata, and Triad. Manage research project databases, utilize team flow sheets and other study related documents. Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Be able to identify and report study deviations. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed. Serve as primary or secondary contact with, sponsors, and regulatory agencies. Coordinate collection of study specimens and processing. Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact. 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. Other duties may also be assigned Job Requirements: Knowledge of medical terminology. 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. 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. Proficiency with Microsoft Office. Highly detail oriented Strong interpersonal skills. Comfortable reading medical charts and data entry Qualification & Experience: Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. 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. Job Details: Company: Stanford Vacancy Type: Full Time Job Location: Manchester, NH, US Application Deadline: N/A Apply Here careers-trivia.net
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