CRA Monitor: Site Liaison & Trial Monitoring
Dan Cummins Ford Lincoln
Planet Group is seeking a Clinical Research Associate (CRA) to monitor trials and manage relationships with investigative sites across the Midwest and East Coast. The CRA ensures participant safety, data integrity, and adherence to ICH GCP and Sponsor SOPs, coordinating with IHCRA and RSU teams as needed. The role requires graduate-level life sciences knowledge, strong organization, and team collaboration, with flexibility for onsite or remote monitoring as required by the study protocol. #J-18808-Ljbffr Dan Cummins Ford Lincoln
- ...Research Associate II in the Mid-West. As a CRA II at ICON, you will design and analyse clinical trials, interpret complex medical data, and... ...treatments and therapies. Key duties include site qualification, initiation, monitoring, and close-out visits, ensuring protocol...Website
- CRA Monitor (Midwest + East Coast) job at Planet Group. Chicago, IL. The Clinical Research Associate... ...for ensuring the rights & wellbeing of trial participants are protected and the... ...primary contact between the Investigational Sites and Sponsor. Key responsibility of a CRA...WebsiteLocal areaRemote work
- ICON plc in Chicago seeks a Senior Clinical Research Associate for Oncology Phase I to manage investigative sites and monitor trials, ensuring data integrity and subject safety. You will perform site qualification visits, maintain inspection readiness, and collaborate...Website
- ...Research Associate II role in the Midwest involves designing and analyzing clinical trials, interpreting complex medical data, and contributing to innovative treatments. You will monitor sites, ensure protocol compliance, and work with investigators to ensure high-quality...Website
- ...Clinical Research Associate with ophthalmology expertise to oversee site performance and regulatory compliance for assigned protocols... ...across all phases. The role includes expanding territory, monitoring visits, site selection input, and collaboration with cross-functional...WebsiteRemote jobLocal area
- ...Clinical Research Associate for a small CRO focused on US-based studies. The role involves independently performing site selection, initiation, routine monitoring, and close-out visits in accordance with protocol and ICH-GCP guidelines. You will manage a defined caseload...Website
- The University of Chicago Medicine Comprehensive Cancer Center is seeking a Clinical Research Monitoring Specialist to manage and support daily clinical research and trial activities. You will collect, document, analyze, and report data while ensuring compliance with FDA...Remote jobLocal area
$65k - $80k
...marketing and communications, fundraising, data analytics, clinical trials management, and community outreach and engagement. The UCCCC... ...trials each year. Job Summary Manages, facilitates, and monitors daily clinical research and clinical trial activities. Performs...Work experience placementWork at officeLocal areaRemote work- ...Biological Sciences Division at the University of Chicago is seeking a clinical research monitor within the BSD CCC - Quality Core. The role supports daily clinical research and trial activities, collecting, documenting, and reporting data to inform decisions across the...
- ...Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization... ...conduct, and interpretation of clinical trials. This includes serving as the primary... ...medical point of contact for investigative sites and sponsors, and providing real-time...Website
- ...as the primary contact between investigational sites and sponsors, managing site visits, ensuring compliance... ...or equivalent, at least 2 years of on-site monitoring experience, and a strong background in Oncology clinical trials. ICON offers a competitive salary and diverse...WebsiteWork at office
$16.49 - $24.44 per hour
...more than 1,500 physicians throughout Cook, Will and DuPage counties. All three of our hospital sites are within a short commute from the city! If you are a Cardiac Monitor Tech who’s interested in working for a regional leader in healthcare, delivering compassionate care...WebsiteHourly payFull timeWork experience placementSecond jobLocal areaImmediate startShift workNight shift$145.6k - $270.4k
...medicine at scale? As a Precision Medicine Liaison, you will play a critical role in... ...areas.Execute diagnostic, prognostic, and monitoring workflow initiatives across assigned healthcare... ...diagnostic workflows across sites, departments, and service lines within integrated...WebsiteFull timeLocal areaRemote work- ...all methods of medication administration. Maintains IV access according to hospital policy and procedures. Assesses and documents IV site every eight hours per unit standard. Reports change in patient status immediately. Reports the progress of the patient’s/significant...WebsiteReliefImmediate start
- Loyola Medicine, a member of Trinity Health, is seeking a Cardiac Monitor Tech for a Full time, 12 Hour Night Shift position in the... ...rhythm changes, document patient information, and manage supplies on site. Required: EKG certification or class completed; minimum education...WebsiteFull timeNight shift
- Equip for Equality Inc. in Chicago seeks an experienced clinical professional to monitor safety and quality of care for people with disabilities in Illinois. The role involves on-site monitoring in facilities and community programs, collaboration with a monitors team,...WebsiteRemote job
- ...quality of care for people with disabilities in Illinois. The position involves working collaboratively with a team of monitors and includes on-site monitoring in facilities and community programs to help ensure that individuals with disabilities have successful community...WebsiteWork at officeLocal areaRemote workFlexible hoursNight shift
- Federal Work Study - Music Room Monitor Harold Washington Campus - Music and Humanities Department City Colleges of Chicago (CCC), the largest... ...in Illinois, is made up of seven colleges and five satellite sites, providing more than 70,000 students each year access to a...WebsiteFull timePart time
$90.2k - $175.1k
...driven Clinical Research Associate (CRA) to join our team and play a key... ...high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional teams to ensure... ...You’ll DoLead and execute site monitoring visits (selection, initiation, routine...WebsiteFull timePart timeImmediate startWorldwide$87.2k - $145.3k
IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience:Essential FunctionsPerform site monitoring visits (selection, initiation... ...) site documents are available for filing in the Trial Master File (TMF) and verify that the...WebsiteFull timePart timeLocal areaImmediate startWorldwide$71.9k - $145.3k
IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor. IQVIA Biotech... ..., you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations...WebsiteFull timePart timeImmediate startWorldwide- ICON plc is seeking a Clinical Research Associate I in Chicago, IL to support clinical trial monitoring across Central/Mid-West regions. You will work with the team to deliver high-quality outcomes, set up studies, monitor progress, and prepare study documentation. Required...
- ...Coordinators wanted at Medpace! Become a CRA and join our growing team!This is... ...qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocolCommunication... ...) through our integrated Clinical Trial Management System to identify site...WebsiteContract workWork at officeRemote workWork from home
- ...Office or Assigned Facility Type: On-Site 5 days a week Short distance travel to... ...OBJECTIVE: The Collections Services Liaison reports directly to the Sr. Collections Manager... ...Collections Services Liaison is responsible for monitoring the AR Aging daily, updating the...WebsiteWork at officeImmediate start
$104.8k - $192.2k
...Role Description Role Family OT Operations Architecture / Monitoring & Tooling Primary Focus OT monitoring, asset visibility,... ...management, network/security operations, SOC teams, vendors, and site stakeholders to improve monitoring coverage, platform health,...WebsiteSummer holidayRemote workFlexible hours$87.2k - $169.3k
...Sr. CRA 1 IQVIA Biotech is seeking Sr. CRA 1 candidates with a minimum of 2 years of on-site monitoring experience in oncology. IQVIA Biotech is a full-service CRO purpose-built... ...documents are available for filing in the Trial Master File (TMF) and verify that the...WebsiteFull timePart timeLocal areaImmediate startWorldwide- ...seeking a Clinical Research Associate to serve as the primary liaison between investigational sites and sponsors, conducting site visits and ensuring ICH-... .... You will manage documentation in CTMS and eTMF, monitor patient safety, and support site staff training while coordinating...Website
- Merck & Co. is seeking a qualified candidate to oversee site management for clinical research programs. The role emphasizes ensuring compliance with ICH-GCP and country regulations, acting as primary site contact, and expanding the site network across assigned territories...Website
$70k - $110k
...and maintenance of structural and geotechnical instrumentation & monitoring systems. In this hands-on role, you will work closely with the... ...safety of yourself and others in every decision you make on site. Actively participate in Sixense’s Health and Safety Program...WebsiteTemporary workFor subcontractorLocal areaNight shift$96.2k - $151.4k
...compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures... ...meetings and workstreams as SME for monitoring processes and systems.... ...relationships through all phases of the trial. Performs clinical study site...WebsiteFor contractorsLocal areaRemote work2 days per week3 days per week
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