Clinical Research Monitor: Site Trials & Data Integrity
Avery Healthcare Group Ltd.
Avery Healthcare Group Ltd. is seeking a qualified candidate for a site monitoring position in Littleton, Colorado. The role includes managing study site practices and ensuring compliance with Good Clinical Practice (GCP) standards. Ideal candidates will have a Bachelor's degree in a scientific discipline, at least 2 years of relevant monitoring experience, and effective communication skills. This position offers an opportunity to contribute to important clinical research projects. #J-18808-Ljbffr Avery Healthcare Group Ltd.
$121.93 - $170.71 per hour
...System Vice President, Clinical and Industry Trials at CommonSpirit Health,... ...investigator-initiated research, industry-sponsored trials... ...patient recruitment, and data integrity across all sites, and will identify and cultivate... ...by the health system. Monitor emerging trends in...DataWebsiteContract workTemporary workWork experience placementLocal areaRemote work$50 - $55 per hour
...implementing mobile clinical nurse services to... ...in clinical trials. Science 37’s extraordinary... ..., clinical researchers, patient recruitment specialists, data managers and technology... ...independently and integrate well with the... ...brick‑and‑mortar sites when indicated, ensuring...DataWebsiteHourly payDaily paidLocal areaRemote workNight shift2 days per week1 day per weekWeekday work$114k - $210.9k
Experienced Clinical Trial Manager - Full-Service Syneos... ...a leading fully-integrated life sciences... ...Responsibilities Responsible for site management oversight, clinical monitoring and central... ...compliance and data integrity.... ...conduct of a clinical research project. Demonstrates...DataWebsiteContract workFlexible hours- ...located. Perform monitoring and site management work to... ...reporting study data as required by the... ...of work and Good Clinical Practice. Work... ...the quality and integrity of study site practices... ...filing in the Trial Master File (TMF)... ...applicable clinical research regulatory...DataWebsiteLocal area
- ...Sr. Directors Of Trial Management Or Executive Director, Clinical Trial Management Medpace... ...check specifications, data analysis plan, and final... ...vendor Manage site quality, including direct... ...supervision of project Clinical Research Associates and monitoring deliverables...DataWebsiteContract workLocal areaImmediate startFlexible hours
- ...looking for: At Least 3 years of device monitoring experience Proficient in Microsoft... ...may be assigned. Monitors progress of clinical trials at the site level or headquarters and ensures... ...with clinical investigators, clinical research organizations (CRO), affiliated hospitals...WebsiteLocal areaRemote work
- ...Clinical Trial Associate Anywhere Type: Consulting Category:... ...CROs, vendors, and clinical sites. The position reports to the... ...Collaborate with Clinical Data Management and Digital Informatics... ...of experience in a clinical research environment. Basic understanding...DataWebsiteHourly payLocal areaRemote workShift work
$59k - $100k
...accuracy and validity of clinical research data for assigned clinical studies... ...for methodically monitoring the status of study subjects... ...procedure. Maintains study site environmental integrity including safe handling... .... Completes the clinical trials management system and electronic...DataWebsiteContract workWork experience placementWork at office- ...solutions organization, is looking for an Experienced Clinical Research Associate. This role involves conducting site qualification, managing monitoring activities, and ensuring regulatory compliance throughout the clinical trial lifecycle. The ideal candidate should have a...Website
$70k - $90k
...looking for a Drug Supply/Clinical Trial Supply Manager to join... ...s) (IP) for CPC Clinical Research clinical trials. This includes... ...sourced products Monitor inventory levels at sites and depots through the life... ...Outlook, etc.), Electronic Data Capture systems Demonstrated...DataWebsiteContract workLocal areaImmediate startRemote workFlexible hours- ...Health Commercial LLC is seeking an Experienced Clinical Research Associate dedicated to managing sites throughout clinical trials. The role requires expertise in site... ...guidelines and protocols, maximizing patient data integrity. This position emphasizes strong communication...DataWebsiteRemote job
- ...currently looking for a Clinical Research Associate to join... ...be responsible for monitoring clinical trials and ensuring... ...FDA guidelines · Data quality on initial review... ...the capability of the site to successfully manage... ..., investigator integrity, and compliance with...DataWebsitePermanent employmentWork from home
$50 - $55 per hour
...implementing mobile clinical nurse services to... ...in clinical trials. Science 37’s extraordinary... ..., clinical researchers, patient recruitment specialists, data managers and technology... ...independently and integrate well with the... ...brick and mortar sites, if indicated, for...DataWebsiteHourly payDaily paidLocal areaRemote workNight shift2 days per week1 day per weekWeekday work$50 - $55 per hour
...implementing mobile clinical nurse services to... ...in clinical trials. Science 37's extraordinary... ..., clinical researchers, patient recruitment specialists, data managers and technology... ...independently and integrate well with the... ...brick and mortar sites, if indicated, for...DataWebsiteHourly payDaily paidLocal areaRemote workNight shift2 days per week1 day per weekWeekday work$32 - $40 per hour
...mission support. As a Security Monitor, you will be responsible for the security and integrity of the facilities. Amentum will... ...to work on restricted customer site. High School diploma or equivalent... ...skills, internal equity, market data, applicable collective bargaining...DataWebsiteHourly payFull timeContract workTemporary workLocal area- ...Kerlo Research Inc. is a privately held Site Management Organization (SMO) with... ...overseeing and coordinating clinical research activities... ...into clinical trials and ensure... ...Collect and manage study data, ensuring accuracy and... ...and study databases. Monitor data entry for accuracy...DataWebsiteWork at officeLocal areaRemote work
- Position Elite Clinical Network (ECN) is seeking... ...a dedicated and research-oriented Physician... ...of clinical trials by serving as a Principal... ..., Sponsors, and Monitors to ensure protocol compliance and data integrity. Review and sign... .... Participate in Site Initiation Visits...DataWebsiteDaily paidPart time
- ...eligibility. Presents trial concepts and details... ...accurate and timely data collection, documentation... ...and participates in monitoring and auditing... ...Responsible for education of clinic staff regarding clinical research. May collaborate with Research Site Leader in the study...DataWebsite
- ...GENERAL DESCRIPTION The Clinical Research Coordinator will be... ...Work with the EMR and data management systems to... ...working knowledge of trial design, statistical methods... ...study budgets and monitor invoicing, billing, and... ...payments. Participate in site visits, SIVs,...DataWebsiteWork at officeImmediate startAfternoon shift
- ...Clinical Research Associate – Full-Service Syneos Health is a fully integrated biopharmaceutical solutions organization... ...Perform site qualification, site... ..., interim monitoring, site management... ...subject safety and data integrity. Assess... ...it with the Trial Master File (TMF...DataWebsiteInterim roleLocal areaImmediate startRemote workFlexible hours
- ...responsible for supporting monitoring and site management... ...cross‑functional clinical study teams and... ...of operational data and metrics. KEY... ...Partner with Clinical Trial Liaison (CTL) and... ...CRO Clinical Research Associate (CRA) and... ...maintain data integrity and protocol deliverables...DataWebsiteInterim roleLocal areaRemote work
$87.2k - $169.3k
...IQVIA Early Clinical Development is... ...dedicated Clinical Research Associate (CRA)... ...execution of clinical trials. In this... ...responsible for monitoring and managing clinical sites to ensure... ...contribute to the integrity and quality of... ...clinical research data. Key Responsibilities...DataWebsiteFull timePart timeImmediate startWorldwide- ...Clinical Research Coordinator The Clinical Research Coordinator... ...of daily clinical trial activities. The CRC will... ...(SCRC), the clinical site, sponsor(s), clinical... ...Perform accurate and timely data collection, source... ...initiation meetings, monitoring visits, audit visits...DataWebsiteWork at officeLocal area
$71.9k - $189k
IQVIA Argentina is seeking a Clinical Research Associate to perform site monitoring visits and manage ongoing project expectations. The role requires conducting... ..., and maintaining key documentation for clinical trials. The ideal candidate should possess at least 2 years...Website$60k - $75k
...opportunity for an experienced Clinical Research Coordinator/RN at our... ...eligibility. Presents trial concepts and details... ...accurate and timely data collection,... ...Schedules and participates in monitoring and auditing... ...collaborate with Research Site Leader in the study selection...DataWebsiteTemporary workFlexible hours- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company... ...of clinical trials. This includes serving... ...contact for investigative sites and sponsors, and... ...interpreting safety data, contributing to... ...experience in medical research or clinical development...DataWebsite
- Parexel is hiring a Clinical Research Associate (CRA) in Denver, Colorado. This... ...while collaborating with site teams. The CRA will oversee site selection and training, monitor study progress, and maintain... ...contribute significantly to clinical trials and enhance healthcare...Website
$99.7k - $175.84k
...Systems (RMS), we are driven by innovation and integrity. We believe that by applying the highest... ...(ISR): Harnessing the power of data collection and analysis across air, land,... ...events to verify functionality, perform on site system validation, and ensure seamless integration...DataWebsiteFull timeTemporary workWork experience placementWork at officeFlexible hours$95k - $167.44k
...baseline. Develop and maintain compliant Integrated Master Schedules that accurately and... ...with @Risk, OnePager Pro. Experience with Data Driven Metric compliance requirements and... ...consideration. Ability to work remotely: On‑site full‑time - the work associated with this...DataWebsiteFull timeWork at officeRemote work- ...Experienced Clinical Research Associate - Sponsor Dedicated... ...a leading fully integrated biopharmaceutical... ...Performs site qualification, site... ...initiation, interim monitoring, site management... ...and clinical data integrity at an investigator... ...the ISF with the Trial Master File (TMF)...DataWebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
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