Clinical Trials Data Coord
City Of Hope Hospital Duarte - Comprehensive Cancer Center
DescriptionClinical Trials Data Coordinator - RemoteJoin the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. This full-time remote position entails ensuring data integrity for various research studies. Responsibilities include data abstraction, CRF completion, query resolution, sponsor monitor visit coordination, and maintaining audit-ready data. You will also oversee electronic research records and patient information in the CTMS, contributing to cutting-edge clinical research.As a successful candidate, you will: Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations.Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information.Take responsibility for communicating any protocol deviations or issues related to study execution, ensuring transparency and problem resolution.Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the proper execution of study parameters in accordance with protocol requirements.Seek appropriate supervision, when necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in all aspects of your work.Qualifications - ExternalQualifications - ExternalQualifications - ExternalQualifications - ExternalQualifications - ExternalQualifications - ExternalQualifications - ExternalQualificationsYour qualifications should include: Bachelor’s Degree, relevant experience may substitute for degree.At least two years of experience related to the conduct of oncology clinical trials.Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.City of Hope is an equal opportunity employer.To learn more about our Comprehensive Benefits, pleaseCLICK HERE.Job Field: Clinical ResearchShift: Days
- ...includes its Los Angeles campus, a network of clinical care locations across Southern California... ...CRC) will be responsible for maintaining data integrity of multiple assigned research... ...of patient information in the clinical trials management system (CTMS). The CRC must...DataContract workWork experience placementLocal area
- Clinical Study Coordinator - Clinical Research (On‑Site) Join the transformative team at City... ...Coordinator to support oncology clinical trials. Under the supervision of the Director,... ...recruitment, informed consent, trial coordination, data management, and regulatory compliance....DataFull time
- ...future of medicine through cutting-edge research.City of Hope is seeking a talented Biostatistician I to support clinical trial and observational study data under the guidance of a Ph.D.-level biostatistician. This role contributes to research database development, study...DataWork experience placement
- ...includes its Los Angeles campus, a network of clinical care locations across Southern California... ...the RoleThe Vice President, Clinical Trial Operations (VP CTO) provides strategic,... ...safety, protocol compliance, and accurate data collection.Ensure strong relationships across...DataWork experience placement
- ...future of medicine through cutting-edge research.City of Hope has a Clinical Research Associate II (CRA II) opportunity available. The CRA II... ...documentation of patient registration. Compile and submits data on appropriate forms according to protocol requirements.Ensure protocol...DataWork experience placement
- ...Clinical Research Associate I - Microbiome Program Join the forefront of groundbreaking... ...DSMB, and PRMC/CPRMC. Compile and submit data on appropriate forms according to... ...Record, Health Information Systems, clinical trials exposure or related health field. City...DataHourly payWork experience placementShift work
- ...Clinical Research Associate II Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where... ...be responsible for attending clinics as needed, ensuring smooth data compilation, registration, and submission processes. You will monitor...DataHourly payWork experience placementShift work
- ...Clinical Research Assistant I Join the forefront of groundbreaking research at the Beckman... ...registration. Compile and submit data on appropriate forms according to protocol... ...health information systems, and/or clinical trials is preferred City of Hope employees...DataHourly payWork experience placementShift work
- ...medicine through cutting-edge research. A Clinical Research Associate I role is available... ..., registration and submission of data and maintaining a system for effective data... ...health information systems, and/or clinical trials is preferred * Superb communication and...DataWork experience placement
- ...Duarte Medical Center is seeking a full-time, on-site Clinical Study Coordinator to support oncology trials. This patient-facing role involves coordinating... ...to Phase III trials, handling recruitment, consent, data management, and regulatory compliance in a fast-paced...DataFull time
- City of Hope is seeking a Clinical Research Associate to oversee multiple research protocols, ensuring regulatory compliance and efficient data flow across clinics. You will manage data compilation, registration, submission, and maintain data integrity in a dynamic clinical...Data
- ...University of Southern California Arcadia Hospital is seeking a Research Coordinator to support investigators in subject recruitment, data collection, scheduling, and follow-up of enrolled participants. You will coordinate with IRB, sponsor and study team, ensure...Data
- City of Hope in Duarte, CA seeks a Clinical Research Associate II to manage multiple research protocols, ensuring regulatory compliance and... ...will work with investigators, coordinate patient registration, data collection, and adherence to study timelines. The role supports...Data
- ...Clinical Research Associate I Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where... ...regulatory compliance while attending clinics as needed. You'll handle data compilation, registration, and submission, and maintain an...DataHourly payShift work
- ...coordinating with investigators and regulatory bodies to ensure protocol submissions and compliance. You will oversee databases, maintain data integrity, and support translational research initiatives. Responsibilities include recruiting and consenting participants, ensuring...Data
- ...Clinical Research Associate I - Division of Thoracic Surgery and Health Equity Join the... ...recruitment to studies Collect patient data to enter into databases for studies Collect... ...information systems, and/or clinical trials is preferred City of Hope employees pay...DataHourly payWork experience placementShift work
$30 - $40 per hour
...Job Description Job Description SGV Clinical is part of the Irvine Clinical Research site... ...’s Disease prevention and treatment drug trials, and our doctors were the largest... ...team to ensure the highest standards of data integrity, patient safety, and operational...DataHourly payFull timeImmediate start$34.32 - $56.19 per hour
...Produces reports and other materials, as directed. • Assists with data collection for research studies following established data... .... • Provides ongoing education to study subjects about clinical trials and provides significant new information that may affect a subject...DataHourly payDaily paidFull timeWork experience placementLocal area- ...grant funding lasting 3-5 years from a federal agency. Join us as a Clinical Research Associate, where you'll manage multiple research... ...regulatory compliance while attending clinics as needed. You'll handle data compilation, registration, and submission, and maintain an...DataWork experience placement
- ...Gastroenterology, Cancer Cell, PNAS, JAMA Oncology, JNCI, Cancer Research, Clinical Cancer Research, , Annals of Surgery, etc.For more information... ....· Accurately record work, calculate, compile, and analyze data.· Evaluate research data and suggest improvements, train staff...DataWork experience placement
- ...cutting-edge research. City of hope is in search of a talented Biostatistician I to program and summarize statistical analyses of data from clinical research projects within the Department of Population Sciences and Department of Surgery with some guidance from a Ph.D....DataHourly payWork experience placementShift work
- Job Details: Job Location: Pasadena Clinic - Pasadena, CA 91107, Salary Range: $23.00 - $... ...aspects of patients involved in clinical trials. Ensure procedures are completed properly... ...trials. Responsible for accurate and timely data collection, documentation, entry, and...DataHourly payWork at officeLocal area
$25 - $30 per hour
...About Us: Flourish Research is where clinical trials thrive. Flourish Research is one of the industry's most progressive and diversified... ...vital signs, ECG/EKG, etc. Document assessments and study data per regs/GCP Obtain and document informed consent following...DataHourly payWork at officeMonday to FridayFlexible hoursShift workDay shift$104k - $160k
...procedures. Participates in all MRI and/or Radiation Oncology related clinical research protocols and ensures that patient and staff safety is... .... Prepares room and equipment for patient Enters patient data at the start of examination and monitors data acquisition during...DataFull timeLocal areaRelocation packageDay shift$63k - $156.2k
...trusted partners. • Utilizes appropriate business insight tools, data, and analytics to identify trends, priorities, opportunities,... ...learning agility to understand disease state, marketplace, clinical trials, and product label. • Promotes the BU portfolio by planning...DataFull timeH1bVisa sponsorshipWork visaFlexible hours- QC & Data Analyst - Covina, CA Location: Covina, California, United States About The Job Ready to take your clinical research experience into a role focused on quality, data and study accuracy... ...play a key role in ensuring clinical trial data is accurate, complete and...Data
- ...Assistant Clinical Research Coordinator Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all infrastructure... ...coordination, patient interaction, data collection, and clinical procedures...DataWork at office
- ...Help Advance Clinical Research Through Strong Financial and Contract Management We are... ...support the successful execution of clinical trial agreements. This position is ideal for someone who enjoys analyzing financial data, negotiating agreements, managing complex...DataFull timeContract workWork at office
- Green Life Science in Covina, California, is seeking a QC & Data Analyst to ensure data accuracy and regulatory compliance across clinical trials. You will review study charts, manage CRF/eCRF data, perform source-to-CRF reconciliation, and support data queries. The role...Data
$30 - $38 per hour
...or an alternative application process. Clinical Research Coordinator II Full Time Front Office... ...to the preparation and gathering of all data and documents for this highly regulated... ...best suited to a coordinator who has run trials with significant independence at a...DataHourly payFull timeWork at officeFlexible hoursNight shift
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