Clinical Research Associate - Site Monitoring & Trials
IQVIA
IQVIA is seeking a Monitoring Scientist to perform on-site monitoring for clinical studies in the United States. You will ensure sites conduct studies according to protocol, GCP and sponsor requirements, and support site recruitment and data quality. Responsibilities include visits (initiation, monitoring, close-out), communication with sites, maintaining TMF/ISF, and generating visit reports. Strong English, organizational, and time-management skills are essential. #J-18808-Ljbffr IQVIA
- Abbott is seeking a Clinical Research Associate I to ensure quality and integrity of clinical trial data across multiple studies in Alameda, CA. This on-site role supports site monitoring, data listing reviews, and regulatory submissions within a leading healthcare company...Website
- ...in Alameda, California is seeking a Clinical Research Associate I to ensure data quality and integrity across multiple trials. The role is on-site and requires travel up to 30-50% with... ...management support for study startup, monitoring, and regulatory activities. The candidate...Website
- ...requires 5 years of experience in clinical research, including a minimum of 2 years field monitoring experience and 3 years in lead... ...terminology, protocol, clinical trial process, regulatory requirements... ...Ability to establish rapport with site personnel/ colleagues....Website
- ...Clinical Research Associate To be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the... ...for filing in the Trial Master File (TMF) and verify...WebsiteLocal area
- ....Job Description SummaryJob DescriptionROLEThe Clinical Research Associate is an important member of the Alira Health Clinical... ...and function independently to conduct site monitoring responsibilities for clinical trials. CRAs work closely with the In-house CRAs, Lead...WebsitePermanent employmentFull timeInterim role
$81.5k - $141.3k
...timeCategory: Medical and Clinical AffairsIndustry:... ...revolutionizing the way people monitor their glucose levels... ....As the Clinical Research Associate II, you will assist in... ...to potential research sites and evaluate their ability... ...to perform ADC trials.Present research protocols...WebsiteFlexible hours$90.2k - $175.1k
...minimum of 1.5 years of onsite monitoring, and early phase experience... ...are seeking a dedicated Clinical Research Associate (CRA) to join our team and... ...successful execution of clinical trials. In this position, you will... ...and managing clinical sites to ensure compliance with...WebsiteFull timePart timeImmediate startWorldwide- ...Senior Clinical Research AssociateIQVIA is now hiring for a Senior Clinical Research Associate located on the West Coast, US to join... ...execution of clinical trials. In this position you... ...will be responsible for monitoring and managing clinical sites to ensure compliance...WebsiteImmediate start
$45 - $55 per hour
...pay range $45.00/hr - $55.00/hr Clinical Research Associate Status : Contract - 6 months Comp... ...compliance. The CRA will manage monitoring activities across all trial phases and collaborate closely with... ...Responsibilities Conduct comprehensive site monitoring (start-up, initiation,...WebsiteHourly payContract workWork at office$73.9k - $116k
...Clinical Research AssociateAbbott is a global healthcare leader that helps... ...accuracy and integrity of clinical trial data throughout the full... ...and ISO14155.This is an on-site position in Alameda,... ...SQV, SIV, IMV, COV), generate monitoring reports, and track resolution...WebsiteInterim roleWorldwide- Abbott Laboratories in Alameda, California is seeking a Clinical Research Associate I to support clinical trials, monitor site activities, and ensure protocol compliance under supervision. You will collaborate with cross-functional teams, assist with data collection and...Website
- ...record is seeking a motivated Clinical Research Associate for a hybrid role at their San Francisco site. Their commercial supply of... .... Since their first clinical trials in 2006, they've had 3 approvals... ...aspects of clinical monitoring and site management 20-25% travel...WebsiteFull timeLocal area
$72.1k - $114.7k
Clinical Research Associate I job at Abbott. Alameda, CA. Abbott is a global healthcare... ...and integrity of clinical trial data throughout the full... ...ISO14155. This is an on-site position in Alameda, California... ..., SIV, IMV, COV), generate monitoring reports, and track...WebsiteInterim role$89k - $130k
...assists in the execution of clinical studies sponsored by... ...Serve as the site manager, ensuring data... ...site. Participate in the monitoring functions in a clinical... ...at both the sites and trial master file, and for audit... ...in clinical/scientific research, nursing, or medical devices...WebsiteTemporary workWork at officeLocal areaRemote work$60k - $140k
...Clinical Research Coordinators Wanted At Medpace! This is an... ...fill Clinical Research Associate (CRA) openings with Medpace... ..., initiation, monitoring, and closeout visits at research sites in compliance with the... ...our integrated Clinical Trial Management System to identify...WebsiteFull timeContract workTemporary workWork at officeRemote workWork from homeHome officeFlexible hours$49.48 - $60.16 per hour
...Clinical Research Associate ~ Oakland, CA ~ Highland General Hospital ~ FQHC HGH HCP 5 ~ Temporary... ...coordinates all aspects of clinical trials within the assigned unit.at the Adult... ...for selecting, implementing and monitoring clinical trials, educating, and when...Full timeTemporary work$91.34k - $114.17k
Clinical Research Associate - Cross Therapeutic - Northwest RegionICON is a global healthcare intelligence... ...of contact between investigational sites and the sponsorConduct all types of... ...including selection, initiation, routine monitoring, and close-outEnsure site compliance...WebsiteFull timeLocal area- ...Clinical Research Associate - Cross Therapeutic - Northwest Region At ICON Strategic Solutions, you... ...point of contact between investigational sites and the sponsor Conduct all types... ...selection, initiation, routine monitoring, and close-out Ensure site compliance...WebsiteLocal areaWorldwideVisa sponsorshipFlexible hours
- ...Overnight Shelter Monitor - Taimon Booton Navigation Center San Francisco Community Health Center is a federally qualified health center... ...are responsible for the operation and security of the shelter site and the supervision of the shelter guests. The shelter operates...WebsiteFull timePart timeSeasonal workImmediate startShift workNight shiftWeekend workDay shiftAfternoon shift
- Flourish Research in Walnut Creek, CA is hiring a Research Assistant to support our clinical trials team at the Walnut Creek site. The role involves patient visits, phlebotomy, IVs, vital signs, ECG, and data collection in line with ICH, FDA, and GCP standards. You will...Website
- ...Monitor Technician As a member of a patient care team, and under the direction of the Registered Nurse, the Monitor Technician is primarily... .../EKG test standardized by the Employer which will be taken on site in computerized format. Must demonstrate effective written...Website
$90k - $108k
...unique opportunity for an entry-level Clinical Operations Professional. The Clinical Trial Assistant of Clinical Operations,... .... Gathering investigator and site information, to support study... ...clinical operations or clinical research. Experience of Global clinical trial...WebsiteFull timeLocal areaWorldwide- ...II to assist in executing sponsored clinical studies evaluating device safety and... ...This role involves data management at sites, coordinating monitoring activities, and ensuring regulatory... ...The candidate will travel 30-60% to research laboratories or hospitals and...Website
- Caribou Biosciences, Inc. seeks a Clinical Trial Manager to drive operational execution for global trials in a fast-paced environment. You will oversee study start-up, site qualification, monitoring, data quality, and trials close-out, ensuring compliance with ICH-GCP...WebsiteRemote job
$25 per hour
...Job Description Job Description Description: JOB SUMMARY: The Diplomat/Care Monitor works closely with onsite staff, providing support and monitoring of the site to ensure a safe environment for staff and residents. Site Monitor reports to the Site Manager....WebsiteHourly payFull timeLocal areaFlexible hoursShift workNight shiftWeekend workDay shiftAfternoon shift- Sr. Clinical Research Associate Location: MidwestAre you looking for a sponsor-side... ...the success of clinical trials across multiple studies. This... ...puts you at the center of site oversight, data integrity,... ...feasibility, selection, initiation, monitoring, and close-out...WebsiteWork at officeRemote work
$175k - $210k
...customer-facing observability products within Crusoe Cloud's Cloud Monitoring Service. This team delivers the managed logs experience and... ...Collaboration: Work closely with product, cloud support, and site reliability teams to understand where customers get stuck, and...WebsiteFull timeTemporary work$145k - $165k
Caribou Biosciences is a leading clinical-stage CRISPR genome-editing... ....We are seeking a Clinical Trial Manager (CTM) to join our Clinical... ...studies, including study/site feasibility, start-up,... ...maintain high standards for site monitoring and trial executionManage operational...WebsiteLocal areaRemote work$72.1k - $114.7k
...Abbott in Alameda, CA is seeking a Clinical Research Associate I to ensure data integrity in clinical trials. This role involves conducting site visits, assisting with study management, and ensuring compliance with regulations. The ideal candidate holds a BS in life sciences...Website$135k - $165k
...Required: 5% Reports To: VP, Clinical Operations Department:... ...operational data. The Clinical Trial Manager will report to the... ...ensures compliance with clinical monitoring plan and associated key performance indicators... ...vendors and investigative sites. Provides vendor oversight...WebsiteFull time
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