Clinical Research Data Coordinator II- Cancer Clinical Trials OfficeRequisition # 20001919 Apply Now
Cancer Research Breakthroughs Begin in our Labs with Employees Just Like You
Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements. Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our researchers develop some of the most advanced clinical trials in the world. Here, you will be a part of leading-edge cancer research history that improves our cancer patients' treatment options, one trial at a time.
Do you have a passion for helping human kind?
As a member of our Cancer Clinical Trials Office (CCTO) at the Samuel Oschin Comprehensive Cancer Institute (SOCCI), you will bring your dedication and expertise to collaborate on cancer trials and assist on cancer research studies. You will provide support and service to faculty and staff conducting oncology research. This includes coordination of staff support, provision of centralized systems, regulatory expertise, and quality assurance. Your work will support our mission of rapidly translating research discoveries into safe, effective treatments.
You will work in coordination with Clinical Research Coordinators, Research Program Administrators and Research Nurse Coordinators.
As a Clinical Research Data Coordinator II, you will also be responsible for the following:
- Ensure compliance with protocol and overall clinical research objectives, while maintaining research practices using Good Clinical Practice (GCP) guidelines
- Collect data from sponsors and enter information into the Electronic Data Systems (EDCs) and complete case report forms (CRFs).
- Evaluate and abstract data from source documents.
- Provide supervised patient contact or patient contact for long term follow-up patients.
- Assist with regulatory submissions to the Institutional Review Board (IRB) and work closely with supervising research staff or directly with the IRB to submit the following: adverse events, serious adverse events, and safety letters.
- Schedule patients for research visits and research procedures.
- Manage samples, including preparation, shipping, and maintenance of study supplies and kits.
- Maintain strict patient confidentiality according to HIPAA regulations and all laws.
- Participate in professional development training and continued education programs.
- May serve as the point of contact for external sponsors for select trials.
ACRP/SoCRA (or equivalent) certification preferred.
Two (2) years of directly related experience, or equivalent combination of education and experience
- Working Title: Clinical Research Data Coordinator II- Cancer Clinical Trials Office
- Department: SOCCI Clinical Research Office
- Business Entity: Academic / Research
- City: Los Angeles
- Job Category: Academic/Research
- Job Specialty: Research Studies/Clinical Trials
- Position Type: Full-time
- Shift Length: 8 hour shift
- Shift Type: Day
Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at Applicant_Accommodation@cshs.org and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.
Cedars-Sinai will consider for employment qualified applicants with criminal histories, in accordance with the Los Angeles Fair Chance Initiative for Hiring.
At Cedars-Sinai, we are dedicated to the safety, health and wellbeing of our patients and employees. This includes protecting our patients from communicable diseases, such as influenza (flu). For this reason, we require that all new employees receive a flu vaccine based on the seasonal availability of flu vaccine (typically during September through March each year) as a condition of employment, and annually thereafter as a condition of continued employment.
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