Job DescriptionThe Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing innovative therapeutic options to all of our patients with cancer!Join our team and contribute to groundbreaking research!The Clinical Research Data Associate III manages the data for assigned research studies. This will include, crafting forms for data collection, clinical data abstraction, processing data, maintaining record systems, and producing project reports for studies. In addition, may supervise clinical research staff or clinical data managers, perform sophisticated statistical analysis, and work with bioinformatics to develop and maintain trial management and validation systems. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.Primary Duties and ResponsibilitiesSupervise clinical research data specialists, as needed.Work with bioinformatics in the development and maintenance of clinical trials management systems including validationof systems, as needed.Train clinical research staff to help improve the quality of the data being collected, as needed.Solve operational/data problems in consultation with other employees and/or supervisors, as needed.Plans and prepares the team for study audits and delegates task to team members to ensure audit readiness.Participates in the study audit process and coordinates the vital follow up with the study team.Coordinates data for research studies.Crafts forms for data collection.Performs clinical data collection/abstraction.Processes clinical data using a range of computer applications and database systems to support cleaning and management of subject or patient data.Produces project reports.Performs data searches and other related administrative tasks.Participates in required training and education programs.Works closely with study monitors to review study data and respond to inquiries.QualificationsHigh School Diploma/GED (Minimum)Bachelor's Degree BA/BS degree in science or science related field. (Preferred)Experience:5 years In related experience required.About UsCedars-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. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents.About the TeamWith a growing number of primary urgent and specialty care locations across Southern California, 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.Req ID : 3998Working Title : CMCF 1102083 Angeles Research Inst Clinical Research Data Associate III FR 62655 Hann M19 1.00Department : Angeles Research InstBusiness Entity : Cedars-Sinai Medical CenterJob Category : Academic / ResearchJob Specialty : Research Studies/ Clin TrialOvertime Status : NONEXEMPTPrimary Shift : DayShift Duration : 8 hourBase Pay : $25.87 - $40.10Cedars-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.
