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Clinical Research Coordinator

Company: Stanford University
Location: Stanford
Posted on: May 20, 2019

Job Description:

Clinical Research Coordinator Stanford University Job Number: 82573 Join a dynamic team and support a wide variety of research across the School of Medicine The Stanford Center for Clinical Research (SCCR) is hiring 1-2 Clinical Research Coordinator 1 positions to support multiple clinical research studies throughout the School of Medicine. SCCR provides infrastructure and support to Clinical Research Investigators and Staff throughout the Department of Medicine and School of Medicine and aims to promote high-quality, globally impactful clinical research. We are a large and growing team with an emphasis on quality, effective operations, and a supportive environment. The Coordinator may work across multiple therapeutic areas and Principal Investigators, depending on the studies available at a given time. The Clinical Research Coordinator 1 will perform duties related to the coordination of clinical studies. Coordinate moderately complex aspects of one or more clinical studies. Provide guidance to less experienced staff, and work under the general direction of the principal investigator and/or study coordinator/supervisor. 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. - Other duties may also be assigned DESIRED QUALIFICATIONS: Knowledge of FDA regulations, IRB requirements, and Good Clinical Practice. Experience with Word, Excel, Eudora/Outlook, databases, data management and medical terminology. Experience working with health care professionals and clinical research participants Possess strong organizational skills and a demonstrated ability to work independently with minimal supervision as well as cooperatively in a team environment. Excellent problem-solving skills. Demonstrated proactive approach to developing efficient systems and processes, and addressing barriers Ability to work effectively with a wide range of individuals and groups at all levels of authority. Proven capacity to set priorities, coordinate multiple assignments, work in a fast paced, multi-tasked environment, exercising sound judgment in setting priorities with a strong attention to detail. EDUCATION & EXPERIENCE (REQUIRED): 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. KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED): Strong interpersonal skills. Proficiency with Microsoft Office. Knowledge of medical terminology. CERTIFICATIONS & LICENSES: Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. PHYSICAL REQUIREMENTS: 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. - 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. WORKING CONDITIONS: Occasional evening and weekend hours. WORK STANDARDS: 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. Job Family: Research Job Series: Clinical Research Coordinator Job Code: 4924 Grade: F Exemption: Non-exempt Schedule: Full-time Additional Information Schedule: Full-time Job Code: 4924 Employee Status: Regular Grade: F Requisition ID: 82573 Job: Location: School of Medicine, California, United States Schedule: Classification Level: To be considered for this position please visit our web site and apply on line at the following link: stanfordcareers.stanford.edu Stanford is an equal opportunity employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by law. Copyright --2017 Jobelephant.com Inc. All rights reserved. Posted by the FREE value-added recruitment advertising agency jeid-b015676107f8684eb37fa3b6c5b93ba5

Keywords: Stanford University, San Francisco , Clinical Research Coordinator, Accounting, Auditing , Stanford, California

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