Clinical Research Coordinator II Specialist
hace 2 semanas
Cedars-Sinai seeks a Clinical Research Coordinator II to serve as the lead coordinator on an assigned portfolio of research studies. The ideal candidate will have experience in clinical research coordination and be able to establish and coordinate logistics and processes for the conduct of research projects.
","Responsibilities": "- Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety.
- Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE's and source documents.
- Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process.
- Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution of queries from sponsors or regulatory entities.
- Covers institutional, pharmaceutical, and internal audits, including facilitating third-party study monitoring and designs and implements needed corrective actions.
- Compiles and reports on each study, including information related to protocol activity, accrual data, workload, and other research information; presents this information at regular research staff meetings.
- Submits adverse events, serious adverse events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
- Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality.
- Plans and coordinates strategies for increasing research participant enrollment, and/or improving clinical research efficiency as needed.
- Provides technical support for the preparation of grant proposals, publications, presentations, and special projects.
- Assists with research project budget development, including identifying and classifying routine care vs. research-related care and provides assistance with research participant research billing and reconciliation.
Associate Degree/College Diploma required. Bachelor's Degree preferred. 3 years - Clinical research coordination or related experience, required Basic Life Support (BLS) AHA Healthcare Provider Type Only, required. Certification In Clinical Research - SoCRA or ACRP certification, preferred.
","Company Overview": "Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine, and research. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching, and community service.
","About the Team": "Cedars-Sinai's medical network serves people near where they live. Delivering coordinated, compassionate healthcare, you can join our network of clinicians and physicians to improve the healthcare people throughout Los Angeles and beyond.
","Work Environment": "The incumbent will work in a dynamic and fast-paced research environment with frequent interactions with principal investigators, subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives.
","What We Offer": "Cedars-Sinai offers a competitive salary and a comprehensive benefits package, including medical, dental, and vision insurance, 401(k) plan, and paid time off.
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