Clinical Research Associate I: Oncology Trials & Data
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City of Hope is seeking a Clinical Research Associate I in Medical Oncology to support data abstraction, protocol management, and regulatory documentation for ongoing cancer studies. You will work with teams and institutional resources to ensure accurate data handling and compliance. Responsibilities include assisting PI with protocol updates, coordinating patient recruitment, collecting specimens, and maintaining study files. #J-18808-Ljbffr SupportFinity™
$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Southern California ICON plc is a world-leading healthcare intelligence... ...activities throughout the clinical trial lifecycle. This Sr. CRA role will... ...Oncology clinical trials to ensure data integrity, subject safety, and...DataWork experience placementInterim roleLocal areaRemote workFlexible hours- We are looking to add a Clinical Research Associate to a growing team to help monitor an Oncology trial. This role will start around 20-25 hours weekly with the potential to... ...Sponsor, and clinical sites. Verify source data (SDV/SDR) by cross-referencing original medical...DataFull timeLive inLocal areaRemote work
- Clinical Research Associate I - Medical Oncology Join the forefront of groundbreaking research at City of Hope where... ...diseases. Responsibilities Work on data abstraction and analysis,... ...Health Information Systems, clinical trials exposure or related health field....Data
- ...areas including immunology, oncology and neuroscience - and products... ...striving for excellence in clinical research, turning science into... ...AbbVie as the choice in clinical trials. Focus on site clinical research... ...driving improvement in data integrity, compliance, overall...DataRemote jobContract workTemporary workLocal area
$80k - $125k
...Job Description Join Us as a Clinical Research Associate (Level II) - Make an Impact... ..., spanning 2,700 clinical trials across 100+ countries in... ...subjects' rights, well-being, and data reliability. You will... ...one of the following areas: Oncology, Ophthalmology, Neurology,...DataTemporary workWork at officeRemote workHome officeFlexible hoursNight shift$90k - $130k
A leading clinical research organization is seeking a Clinical Research Associate to manage clinical sites and monitor data for trials. The ideal candidate should have at least 2 years of experience in clinical monitoring and a strong understanding of ICH/GCP guidelines...DataRemote job$60 - $65 per hour
...Clinical Trial Assistant, Clinical Operations W2 Contract Pay Rate: $6... ...clinical program. Reporting to the Associate Director, you will play a... ...Operations or Clinical Research-related experience. Basic understanding... ....g., eTMF, EDC, IRT, CTMS). Oncology experience preferred. #J-188...Hourly payContract work- ...full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation... ..., equipment and staff to conduct the clinical study throughout the study period. Trains... ...site monitoring experience in phase 2/3 trials, ideally with experience of complex...Interim roleRemote work
$109.5k - $153.3k
...corporate goals. Organize and maintain clinical study documentation (e.g., Trial Master Study Files) including... ...appropriate, ensures the integrity of the data submitted on Case Report Forms (... ...of five (5) years of clinical research monitoring experience (including pre...DataFor contractorsLocal areaRemote work- ...A renowned clinical research organization in California is looking for a Clinical Research Associate to oversee monitoring activities for clinical sites. Responsibilities... ...regulatory standards, and ensuring data integrity throughout the trial process. Candidates should have a...DataLocal areaRemote work
- ...known nationally for excellence in research! The Clinical Research Associate I works under the direction of a Clinical... ...through noncomplex tasks such as data collection, prescreening of... ...participants for various clinical trials. Schedules research participants for...DataDaily paidLocal area
- ...monitoring activities for assigned clinical sites, both in person and... ...accuracy, completeness, and data integrity; identify and... .... Monitor assigned clinical trials and sites by reviewing enrollment... ...of experience as a Clinical Research Associate. #J-18808-Ljbffr ProPharmaDataInterim roleWork at officeLocal areaRemote work
- Clinical Research Associate 3 job at V R Della Infotech Inc. California. Senior Clinical Research Associate... ...of clinical research in drug trials, including Good Clinical Practice (GCP... ...approval. Maintain and track clinical study data, monitor Investigator and Sub‑...DataInterim roleWork at officeRemote workShift work3 days per week
- ...PART-TIME CRA to strengthen our clinical operations team in Ventura,... ...Profound knowledge of clinical research processes and medical terminology... ...for monitoring clinical trials and Ensuring that clinical trial... ...Clinical Trial Protocol Ensuring data quality and integrity meet...DataPart timeFreelanceLocal areaRemote work
$91.34k - $114.17k
...healthcare intelligence and clinical research organization. We’re proud to... ...will contribute to clinical trial monitoring activities, taking... ...protocol compliance, data integrity, and patient safety... ...experience as a Clinical Research Associate. In-depth knowledge of...DataWork experience placementFlexible hours$85k - $136k
# reputed company Bilingual Clinical Research Associate (CRA II / Senior CRA) -2.halvolinkBe an Early ApplicantFull... ...750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5... ...subjects' rights, well-being, and data reliability. You will ensure audit...DataFull timeWork at officeRemote workHome officeNight shift- Clinical Research Associate - Full-Service Syneos Health is a fully integrated biopharmaceutical solutions... ...that might affect subject safety and data integrity. Assess site processes per... ...and completeness, reconcile it with the Trial Master File (TMF), and ensure sites...DataInterim roleLocal areaImmediate startRemote workFlexible hours
$90k - $130k
..., TX, WA Vanguard Clinical, Inc. is a Contract Research Organization (CRO)... ...innovation to clinical trial execution through... ...Quality Assurance, Data Management and... ...Clinical Research Associate (CRA) will execute... ...Prior experience with oncological trials strongly preferred...DataPermanent employmentFull timeContract workInterim roleWork at officeRemote workFlexible hours$71.9k - $189k
Clinical Research Associate, Sponsor Dedicated California, United States of America | Full time | Field-... ...(CRF) completion and submission, and data query generation and resolution. May support... ...are available for filing in the Trial Master File (TMF) and verify that the...DataFull timePart timeLocal areaImmediate startWorldwide- A healthcare staffing agency is seeking a Clinical Trial Assistant for a hybrid role in California. This entry-level position offers an opportunity... ...degree and 0-3 years of experience in clinical operations or research. A proactive, detail-oriented approach is essential. #J-18808...
- The Senior Clinical Trial Manager plays a critical role in the strategic planning and execution... ...report (CSR) readiness, supporting complex oncology programs. Oversee CROs, vendors, and... ...and cross-functional activities (e.g., data review meetings). Ensure compliance with...Data
- Job Description The Clinical Trial Assistant (CTA) will provide administrative support to the Clinical Operations Team in the full spectrum of clinical trial activities related to study startup, study maintenance, study closure and vendor management in compliance with...Work at officeLocal area
- ...responsibilities include analyzing specimens, evaluating analytical data, and maintaining laboratory operations. The ideal candidate... ...have strong communication skills and attention to detail, making significant contributions to clinical trials research. #J-18808-Ljbffr IQVIAData
- Direct Jobs is seeking a Clinical Research Associate I in California, Missouri, to assist with the coordination and implementation of noncomplex research... .... Key responsibilities include collecting and evaluating data, scheduling research participants, and assisting with IRB...Data
- Cedars-Sinai is seeking a Clinical Research Associate I to join their team in Missouri. The role involves assisting in the coordination and implementation of research studies, including data collection and IRB submissions. The ideal candidate will have a High School Diploma...Data
- BoneSource in the United States is seeking a Clinical Research Associate I to support coordination of noncomplex studies under supervision. You will assist with data collection, screening participants, and IRB submissions while ensuring compliance with federal and local...DataLocal area
$91.34k - $114.17k
Clinical Research Associate - Multi Therapeutic Area (Early Development) - West Region What You Will Be Doing Serve as the primary point of contact... ...and ensure proper storage, return, or destruction Resolve data queries and drive timely, high‑quality data entry Document...DataWork experience placementLocal areaVisa sponsorshipFlexible hours$136k - $192.5k
Summary The Clinical Trials Manager (CTM), Clinical Operations, coordinates the activities associated with the evaluation, initiation, and management... ...activities of Contract Research Organizations (CROs), and... ...reports, protocol deviations, data review, and other relevant...DataContract workLocal areaFlexible hours- ...Technician works in cooperation with the Farm Manager and the Research Trials Manager to improve the growing conditions of the research crops... ...of the research farm. Responsible for recording seasonal data relating to crop maps, fertilizer, irrigation, and overall growing...DataSeasonal workWork at office
- ...( IRI ) Lead Recruiter at Integrated Resources Inc. (IRI) Sr Clinical Research Spec 100% remote in CA/MN 12 Months+ Preferred location(s): Santa... ...a global study team Basic understanding of biostatistics and trial design Experience in Research and Development (R&D) Ability...Contract workRemote work
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