Site Data & Regulatory Coordinator - Clinical Trials
McKesson
McKesson Corporation is seeking a Site Data and Regulatory Coordinator in Austin, Texas. The role includes providing daily support to Clinical Research teams, ensuring compliance with regulatory documents, and preparing for audits and monitoring visits. The ideal candidate will have knowledge of GCP and regulatory processes, be proficient in MS Office, and possess strong organizational skills. The position offers competitive pay and potential bonuses as part of a comprehensive benefits package. #J-18808-Ljbffr McKesson Corporation
- ...and personalizing treatment. Through clinical excellence and cutting‑edge research... ...The primary responsibility of the Site Data and Regulatory Coordinator is providing support to the Clinical... ...systems for each assigned clinical trial. You will resolve queries for in electronic...DataWebsiteRegulatoryLocal area
- About the Role The Site Data and Regulatory Coordinator provides essential support to the Clinical Research Coordinator (CRC) and Research Nurse, ensuring that all regulatory... ...report forms or EDC systems for assigned trials. Resolve data queries and coordinate with the...DataWebsiteRegulatoryWork at office
- Site Data and Regulatory Coordinator The primary responsibility of the Site Data and Regulatory Coordinator is to provide support to the Clinical Research Coordinator (CRC) and Research Nurse on a daily basis... ...for assigned clinical trials. Resolve queries for electronic...DataWebsiteRegulatoryLocal area
- ...this role, you will join the Regulatory Affairs Department, which provides... ...and allocation. Coordinate and manage relationships with... ...tools and publicly available data, especially on state telecommunications... ...Update SharePoint Regulatory site Partner with the Vice...DataWebsiteRegulatoryWork at office
$65k
...Enterprise Technology - University Data Center Job Posting Title: Information Technology Coordinator I Position Open To: All... ...university owned vehicles to job sites will be required. Maintain acceptable... .... Knowledge of safety and regulatory standards related to installation...DataWebsiteRegulatory16 hoursWork at officeImmediate startRemote workMonday to FridayFlexible hoursShift workNight shiftWeekend work$65k
Information Technology Coordinator I Hiring Department: Enterprise Technology - University Data Center Position Open To: All Applicants... ...owned vehicles to job sites will be required for this position... ...projects. Knowledge of safety and regulatory standards related to...DataWebsiteRegulatoryFull timeFor contractorsWork at officeImmediate startRemote workMonday to FridayFlexible hoursShift workNight shiftWeekend work- .../ Principal Investigator Clinical Research Location: On-site, Austin, Texas 78738 Employment... ...study execution, ensure regulatory compliance, and mentor... ...to drive clinical trial success and organizational... ...Ensure participant safety and data integrity in compliance with...DataWebsiteRegulatoryFull timeMonday to Friday
- ...AVAILABLE Job Title: Full Cycle Clinical Research Coordinator – Alzheimer’s Trials Location: Ocala, FL... ..., sponsors, and regulatory bodies. Key Responsibilities... ...regulatory affairs, and site leadership to initiate Alzheimer... ..., and enter clinical data accurately into EDC...DataWebsiteRegulatoryFull timeRelocationRelocation package
- ...Elite Clinical Network is seeking a compassionate... ...for clinical trial documentation. Maintain... ...and electronic data capture (EDC)... ...Collaborate with study coordinators, investigators,... ...protocols, GCP, and regulatory standards. Assist... ...visits, audits, and site initiation or...DataWebsiteRegulatoryPart timeWork at office
- McKesson is seeking a Site Data and Regulatory Coordinator in Austin, Texas. This role involves supporting the Clinical Research Coordinator and Research Nurse by managing regulatory... ...in Microsoft Office and clinical trial databases is required. Join our mission-driven...DataWebsiteRegulatoryWork at office
- * Conducts site initiation, monitoring, and close... ...with study protocols and regulatory requirements.* Manages... ...Supports participant coordination and visit management,... ....* Coordinates with clinical staff for specimen collection... ...). Familiarity with data entry platforms such...DataWebsiteRegulatoryInternshipWork at officeLocal area
- Parexel in Austin, Texas is seeking a Clinical Research Associate (CRA)... ...overseeing clinical studies at assigned sites. You will ensure compliance with ICH... ...monitor study conduct, and ensure data quality while adhering to all regulatory guidelines. Ideal candidates...DataWebsiteRegulatoryLocal area
- ...SUMMARY: The Clinical Sub-Investigator (... ...execution of clinical trials by ensuring the... ...Practice (GCP), and regulatory standards. Working... ...accurate clinical data, performing... ...collaborate with research coordinators, PIs, and other... ...performance of the clinical site staff Ensure...DataWebsiteRegulatoryLocal area
$40.62k
...Clinical Research Associate I Dell Medical School... ...support for clinical trials by assisting with... ...monitoring activities, data accuracy checks, document... ...by supporting site monitoring visits (remote... ...with Clinical Research Coordinators, regulatory staff, data...DataWebsiteRegulatoryInternshipWork at officeRemote work- ...defining and leading the clinical development strategy of... ...early-phase clinical trials. This role requires a strategic... ...protocols, safety, and data analysis, and leading... ...and submission of key regulatory documents. The role... ..., and trial sites, as well as collaborating...DataWebsiteRegulatory
$68.5k - $217.1k
Join to apply for the Clinical Data Manager role at Katalyst CRO 2 days... ...integrity and quality of clinical trial data from collection through... ..., and compliance with regulatory and protocol-specific requirements... ...collaboration with clinical sites and study teams. Perform...DataWebsiteRegulatoryContract work$33 - $37 per hour
...Looking for a strong Clinical Research Coordinator to join our team! This... ...onsite!!! Clinical Trial Coordination... ...clinical trials from site initiation to close-out... ...and collecting source data using eSource systems... ...complete, accurate, and regulatory-compliant study records...DataWebsiteRegulatoryFull timeContract work- ...Senior Clinical Research Associate - Neurovascular - Midwest... ...plays a critical role in data integrity, patient safety... ...quality of clinical trials conducted at investigative sites. The Senior CRA independently... ...customer SOPs, and applicable regulatory requirements. The Senior...DataWebsiteRegulatoryRemote workFlexible hours
- ...required. Job Purpose: The Clinical Research Associate (CRA... ...studies at allocated sites and is an active... ...for study start-up and regulatory maintenance. Tasks may... ...and other systems with data from study sites as per... ...delivering quality clinical trials with reduced budget and...DataWebsiteRegulatoryLocal areaRemote workFlexible hoursShift work
$50k - $80k
...Medix We are seeking a Clinical Research Coordinator (CRC) to assist with... ...of clinical trials. The CRC will work closely... ...conducted according to regulatory requirements and study... ...study visits and collect data during each visit... ...5,000.00 1 month ago Site Development Specialist...DataWebsiteRegulatoryFull timeRemote work- ...safety of patients in clinical trials and post-marketing settings... ...patient wellbeing and regulatory compliance. About the... ..., labeling documents, data handling conventions,... ...resolve case issues, coordinate with client... ...support to Parexel staff or site (investigator/study coordinator...DataWebsiteRegulatoryInternshipWork at officeLocal areaRemote workWork from homeFlexible hours
$108k - $200k
...Description The Neuralink Clinical team is at the heart of... ...human clinical trials. Our team is built on a... ...compliance with ethical and regulatory protocols, we focus on... ...class clinical research sites. Champion Stakeholder Readiness... ...site engagement. Drive Data Intelligence by leading...DataWebsiteRegulatoryFull timeContract workTemporary workFlexible hours- ...Summary: The Senior Clinical Research Associate (SrCRA... ...studies at allocated sites and is an active participant... ...for study start-up and regulatory maintenance. Tasks may... ...and other systems with data from study sites as per... ...quality clinical trials with reduced budget and...DataWebsiteRegulatoryLocal areaRemote workFlexible hoursShift work
$71.9k - $169.3k
...minimum of 1 year of on-site monitoring and will... ...are seeking a dedicated Clinical Research Associate (CRA... ...execution of clinical trials. In this position, you... ...with study protocols, regulatory requirements, and sponsor... ...quality of clinical research data. Key...DataWebsiteRegulatoryFull timePart timeImmediate startWorldwide$101.6k - $169.3k
...IQVIA is hiring Senior Clinical Research Associate 1 with... ...Perform monitoring and site management work to... ...ies) and reporting study data as required by the study... ...assigned studies by tracking regulatory submissions and... ...available for filing in the Trial Master File (TMF) and...DataWebsiteRegulatoryFull timePart timeLocal areaImmediate start$53.46k
...Clinical Research Coordinator Department of Surgery and Perioperative Care... ...packages, facilitate site initiation, implement... ..., document source data (ALCOA/ALCOA+), enter... ...deviations, execute CAPAs. Regulatory and ethics... ...coordinating interventional trials (oncology, cardiology...DataWebsiteRegulatoryCasual workWork at officeImmediate startRemote workFlexible hours$40k
...Details Job Posting Title: Clinical Research Associate I... ...oversee day to day coordination and operations of assigned... ...of clinical trials to ensure compliance with regulatory requirements and study... ...responsibilities include site management, data collection, and ensuring...DataWebsiteRegulatoryInternshipWork at officeImmediate startAfternoon shift$66.8k - $120k
...Description Join Us as a Clinical Research Associate... ...2,700 clinical trials across 100+... ...opportunity to perform and coordinate all aspects of the... ...monitoring and site management process... ...protocol and regulatory compliance and... ..., well-being, and data reliability. You will...DataWebsiteRegulatoryTemporary workWork at officeRemote workHome officeNight shift- ...implementation of one or more clinical trials and all activities... ...aspects of site investigator grants and... ...the study protocol and coordinates completion of QC review... ...Technology (IRT), Electronic Data Capture (EDC), eDiary... ...with required regulatory and GCP quality standards...DataWebsiteRegulatoryContract workRemote work
- ...Clinical Research Associate The Clinical... ...Wellness Education Coordinators Public Health... ...Manager, Clinical Trial Manager, Training... ...who are medical and regulatory experts; ~ In-house... ...at research sites in compliance with... ...case report form data, including informing...DataWebsiteRegulatoryContract workWork at officeLocal areaImmediate startRemote workWork from homeHome officeFlexible hours
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