Clinical Research Data Coordinator — Reporting & IRB Support
$22.73 - $32.26 per hourMayo Foundation for Medical Education and Research
Mayo Foundation for Medical Education and Research in Phoenix, Arizona, is seeking a Data Coordinator to manage clinical and demographic data essential for enhancing clinical outcomes. The role involves developing and maintaining reports and supporting regulatory needs for clinical trials. The ideal candidate will possess strong expertise in statistical computing and data management, with excellent communication skills. This full-time position offers a competitive compensation ranging from $22.73 to $32.26 per hour, and is eligible for various benefits. #J-18808-Ljbffr Mayo Foundation for Medical Education and Research
- ...Job Summary The Clinical Research Coordinator (CRC) plays a pivotal role in the execution... ...protocols in compliance with IRB, FDA, and GCP guidelines. Maintains data integrity and assists in the... ...completed on time. Tracks and reports adverse events and protocol...DataWork at office
- ...Clinical Research Coordinator II Scottsdale, Arizona At Headlands Research... ...and exceptional support services to broaden outreach... ..., FDA regulations, IRB requirements, and SOPs... ...Ensure timely EDC data entry and resolution of queries Report and follow up on AEs,...DataFull timeLocal areaRemote work
- ...Research Coordinator At United Urology Group, our employees are... ...I, II, III, and IV clinical trials, ensuring protocol... ...Review laboratory data and communicate abnormal... ...them with the PI/SI. Report all Serious Adverse... ...investigator, sponsor, and IRB as outlined in the...DataFull timeWork experience placementWork at officeWeekend work
- ...Clinical Research Coordinator Northwest Valley & Phoenix Locations As a Clinical... ..., documenting, and reporting adverse events, protocol deviations... ...and collection, and IRB reporting guidelines.... ...they will achieve quality data in the most efficient and timely...DataPrivate practiceWork at officeLocal areaFlexible hours
$27.5 - $36 per hour
...through leading clinical trials,... ...quality clinical data. Our network of... ...multitherapeutic research, standard of care... ...Clinical Research Coordinator II or III... ...a resource and support person for subjects... ...and procedure reports Develop and/... ...research, including IRB submissions,...DataHourly payFull timeTemporary workLocal areaMonday to Friday- ...divh2Clinical Research Coordinator I Or II - Thunderbird Office... ...and other vital support staff. We are seeking a Clinical Research... ...in accordance with IRB-approved protocols.... ...assessments, and clinical data into source and electronic... ...liliRecognizes and reports adverse events or...DataWork at office
- ...alternative application process. Clinical Research Coordinator Full Time ISIA - Scottsdale,... ...Institutional Review Board (IRB). Key Responsibilities I.... ...Adverse Events (SAEs). Report all events promptly to the PI... ...high retention rates. II. Data and Documentation Management...DataFull timeWork at office
- Position: Clinical Research Coordinator III Location: Phoenix, AZ Job Id: 1156 #... ...to provide the best quality data to the sponsor. To ensure study... ...to: Sponsor-provided and IRB-approved Protocol Training... ...site(s) Oversee reporting of all Adverse and Serious...Data
- This Clinical Research Coordinator will manage and oversee both the administrative and regulatory aspects... ...reviews. Prepare and submit IRB and committee documents, maintain accurate... ...regulatory documents, fill case report forms, manage data entry and source documentation,...DataFull timeWork at office
$32.38 - $48.17 per hour
...Responsibilities We are seeking a Clinical Research Coordinator to join our team!... ...of clinical research data. Essential Functions... ...person; provide support, recommendations and... ...review board (IRB) and FDA regulations.... ...study modifications; reporting of serious adverse events...Data- Axsendo Clinical Research is a rapidly growing, multi... ...Research Coordinator II to join our team... ...conducting study visits, supporting investigators,... ...Regulatory Compliance Report Adverse Events (... ...(SAEs) to the IRB and sponsor as... ...all study‑related data collection instruments...Data
- ...GRNT | Oncology Research Studies... ...responsible for the coordination of a variety of... ...entry of patient data; maintenance of... ...administrative / regulatory support (recruiting,... ..., processing IRB and other... ...) to specific clinical departments in... ...Completes case report forms, data entry...DataFull timeWork at officeShift work
- ...independently coordinates and is accountable... ...of one or more clinical studies,... ...coordination of research projects from pre... ...entering patient data; maintaining complete... ...and regulatory support—including... ...participants, processing IRB and other... ...Complete case report forms, data...DataWork at office
$26 - $38.55 per hour
...other staff involved in research protocol(s).... .... Position Overview Coordinates non‑therapeutic clinical research protocols with... ...unanticipated problems and reporting appropriately;... ...and entering research data; performing... ...Institutional Review Board (IRB) submission;...DataFull timeMonday to FridayFlexible hours- ## Associate Clinical Research CoordinatorApplylocations... ...Clinical Research Coordinator (ACRC)** to join... ...provide essential support across 7-10 active... ...clinical conduct and data collection and... ...review, training, report production, and submission... ...with all relevant IRB and applicable...DataWork at officeMonday to FridayShift work
$114k - $210.9k
Experienced Clinical Trial Manager - Full‑Service... ...compliance and data integrity.... ...data, metrics and reports to identify risks... ...Data Management to coordinate delivery handoffs... ...Quality Assurance (QA). Supports Inspection Readiness... ...conduct of a clinical research project....DataContract workFlexible hours- ...DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator I to join our team. This individual... ...audits on the clinical data to assess percent... ...Provide consultative support regarding the preparation... ...temperature reporting Develop operating...Data
- ...About the Role: The Clinical Research Coordinator supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols... ...to ensure timely testing and reporting. Collect and assess information on...DataH1bMonday to Friday
- ...consisting of physicians and other vital support staff. We are seeking a Clinical Research Coordinator II or III to join our team. To... ...completion of associated reports/questionnaires. Promotes the... ...projects Excellent organizational, data management, and documentation...DataWork experience placementWork at office
$145k - $180k
...Senior Clinical Project Manager About... ...initiate, execute and report assigned clinical... ...a huge ability to coordinate multiple, parallel... ...submissions to the IRB/EC (local/ central... ...members with a support role (CPCs and CTAs... ...aspects of timely data cleaning, data analysis...DataTemporary workWork experience placementLocal areaRemote workFlexible hours- ..../ph3Position Summary/h3pA Clinical Research Coordinator -Biorepository provides operational and regulatory support for the Caris sponsored studies... ...study enrollment/ accrual reporting, specimen tracking,... ...standard operating procedures, data management plan and/or study...DataWork at officeAfternoon shift
- ...implementation of one or more clinical trials and all... ...scope of work, supports auxiliary service... ...protocol and coordinates completion of QC review... ...site selection, IRB submissions, site... ...(IRT), Electronic Data Capture (EDC),... ...designees' monitoring report review, protocol...DataContract workRemote work
- ...Clinical Research Coordinator At ALS, we encourage you to dream big. When you join... ...of scientific testing and data-driven insights to build a... ...generation of protocols, interim reports, and final reports for... ...excellence. At ALS, you'll be supported to develop new skills and...DataPermanent employmentFull timeInterim roleWork visaFlexible hours
$27 - $36 per hour
...Clinical Research Coordinator II/III We are seeking a motivated Clinical Research... ...Coordinator (CRC) II/III to support and manage clinical trials... ...Accurately enter and maintain study data in CTMS and other systems... ...Monitor patient safety and report adverse events per protocol...DataFull timeContract workTemporary work- ...responsible for the coordination of a variety of research projects from pre-study... ...entry of patient data; maintenance of complete... .../ regulatory support (recruiting, interviewing... ..., processing IRB and other regulatory... ...documents) to specific clinical departments in accordance...Data
- Clinical Research Coordinator - Phoenix, AZ The Clinical Research Coordinator will plan, develop, and coordinate... ...to treatment and communicate data and results to investigators in a timely... ...to generate protocols, interim reports, and final reports for company sponsors...DataPermanent employmentInterim roleWork visa
- Position: Clinical Research Coordinator I Location: Phoenix, AZ Job Id: 1154 # of Openings: 2 Clinic Research... ...limited to: a. Sponsor-provided and IRB-approved Protocol Training b. All... ...trial documentation. Completing data entry and query resolution in a timely...Data
- ...Description About the Role: The Clinical Research Coordinator supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance... ...laboratories to ensure timely testing and reporting. Collect and assess information...DataH1bMonday to Friday
- Clinical Research Coordinator III - Thunderbird Office Arizona Kidney Disease and Hypertension... ...physicians and other vital support staff. We are seeking a... ...audit‑ready study binders, data integrity, and proactive... .... Monitors for and reports adverse events per protocol...DataWork experience placementWork at office
$31.49 - $47.25 per hour
...Why Mayo Clinic Mayo Clinic is top-... .... News & World Report. As we work together... ...position will support Cancer Center... ...involved in research protocol(s). Gives... ...Independently coordinates complex (i.e. interventional... ...after IRB approval and... ...research data to maintain quality...DataFull timeInternshipMonday to FridayFlexible hoursWeekend work
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