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
- ...IQVIA is seeking a passionate Clinical Research Associate (CRA) to enhance clinical trials in Chicago, Illinois. In this role, you'll lead site monitoring visits, ensure compliance with GCP/ICH guidelines, and collaborate with cross-functional teams to manage study execution...Website
- ...performance and compliance for assigned protocols and sites across the country. Working under the CRA-Manager, you will monitor conduct per ICH/GCP, maintain regulatory... ...serve as the primary site contact throughout all trial phases. You will develop site relationships,...WebsiteRemote job
- 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
- IQVIA in Chicago is looking for a passionate Clinical Research Associate (CRA) to impact clinical trials. This role involves site monitoring visits and ensuring compliance with research protocols in accordance with GCP/ICH guidelines. Candidates should have a Bachelor'...Website
- ...primary contact between investigational sites and the sponsor. Responsibilities include... ...ensuring compliance with regulations, and monitoring patient safety. The ideal candidate will... ...research, and familiarity with oncology trials. ICON offers a competitive salary along with...Website
- ICON Strategic Solutions is seeking a Clinical Research Associate in Chicago. The role involves conducting site visits, ensuring compliance, and monitoring patient safety. Ideal candidates will have a Bachelor’s degree or be qualified RNs, along with at least 2 years of...Website
- ThermoFisher Scientific is seeking a Clinical Research Associate (Level II) in Illinois to conduct clinical monitoring and ensure protocol compliance across various sites. This role involves both remote and on-site visits, requiring strong communication and organizational...WebsiteRemote work
$100k - $120k
...Clinical Research Associate in Chicago, IL, to manage investigative sites and ensure the success of clinical studies. The role emphasizes... ...regulatory compliance. Key responsibilities include performing monitoring activities, leading site initiation, and maintaining...Website- Advanced Clinical in Chicago is looking for a Senior Clinical Research Associate (Sr. CRA) to monitor clinical trial sites. Responsibilities include ensuring compliance with protocols, data integrity, and mentoring staff. The ideal candidate should have 3-5 years of clinical...Website
- ...Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing... ...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 medical...Website
- Alimentiv 2 is seeking a Clinical Monitoring leader based in Chicago, Illinois. This role involves overseeing and ensuring high-quality clinical trial execution across global studies. The successful candidate will manage a team while ensuring compliance with all regulatory...Remote job
- ...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
- ...performance and compliance for assigned protocols and sites in the United States. The role reports to the CRA-Manager and ensures adherence to ICH/GCP, local... ...site relationships, conduct on-site and remote monitoring, and coordinate with sponsors to ensure data integrity...WebsiteLocal areaRemote work
$16.49 - $24.44 per hour
...throughout Cook, Will and DuPage counties. All three of our hospital sites are within a short commute from the city! Employment Type Full time Shift Rotating Shift What You’ll Do The Cardiac Monitor Tech provides surveillance of patient cardiac rhythm status as well as...WebsiteHourly payFull timeWork experience placementSecond jobLocal areaImmediate startShift workRotating shift$35 - $45 per hour
...Inc. (Merjent) is seeking highly motivated individuals to perform construction stormwater inspections and environmental compliance site audits in support of energy infrastructure and development projects primarily in the Chicago, IL area. The work environment will consist...WebsiteHourly payContract workFor contractorsRemote workNight shift- ...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
- ...currently seeking a Clinical Research Associate (CRA) for its office in Chicago, Illinois. The CRA will conduct monitoring activities on clinical trials across the country, ensuring compliance and effectiveness in site operations. Candidates should possess 2-4 years of...WebsiteRemote jobWork at office
- ...cross-selling objectives. Focuses on selling CRA products and services, targeting low to... ...identifying, assessing, managing, monitoring, and reporting risks of all types. ESSENTIAL... ...Licensing System (NMLS). The NMLS web site (mortgage.nationwidelicensingsystem.org)...WebsiteDaily paid
$90.2k - $175.1k
...IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in oncology. Join a Team That’s Advancing... ...in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional teams to ensure studies...WebsiteFull timePart timeWorldwide- ...Job Title Health Technician (Telemetry Monitor Technician) Duties Continuously monitors EKGs of patients on telemetry at the Central Station site. Obtains EKG rhythm strips at the beginning of each shift, with new admission to telemetry, every eight hours, and...WebsiteShift work
- ...nursing care team providing continuous observation of telemetry monitoring electrocardiographic (EKG) rhythms of critically ill patients.... ...Continuously monitor EKGs of patients on telemetry at the Central Station site. Obtain EKG rhythm strips at the beginning of each shift, with...WebsitePart timeShift work
$87.2k - $145.3k
...CRA 2 Position IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience: Essential Functions Perform site monitoring visits (selection... ...documents are available for filing in the Trial Master File (TMF) and verify that the...WebsiteFull timePart timeLocal areaImmediate startWorldwide- ...Senior CRA - Oncology - Midwest ICON plc is a world‑leading healthcare intelligence and clinical research organization.... ...the future of clinical development. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory...WebsiteFlexible hours
- Thermo Fisher Scientific in Illinois is seeking a Clinical Research Associate (Level II) to coordinate all aspects of clinical monitoring and site management. You will conduct on-site and remote visits, ensure protocol compliance, manage essential documents, and support...WebsiteRemote job
$71.9k - $189k
...Argentina is seeking a Clinical Research Associate in Oak Brook, Illinois. This full-time role requires at least 2 years of on-site monitoring experience and a Bachelor's Degree in a scientific discipline or health care. The responsibilities include site management, monitoring...WebsiteFull time$71.9k - $145.3k
...CRA 1 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 is a full... ...ensure that assigned study sites conduct trials in compliance with the protocol,...WebsiteFull timePart timeImmediate startWorldwide$66.8k - $120k
..., Illinois. In this role, you'll be responsible for conducting monitoring visits and ensuring compliance with regulatory and protocol standards... ...'ll manage essential documentation and interact with clinical sites to ensure data integrity. The ideal candidate has strong...WebsiteRemote job- ...divisions. You’ll supervise field staff on construction and technical issues, coordinate with vendors, ensure SWPPP and permit compliance, and assist with site audits, training, and project rollouts. Strong regulatory knowledge is essential. #J-18808-Ljbffr Republic ServicesWebsite
$16.2 per hour
...Employment Opportunities Designed to Help Us Collaborate in Creation! MONITOR Thank you for your interest in Loyola University Chicago. To view open positions, please enter your search criteria below. You may view all open positions by not specifying any search criteria...WebsiteHourly payFull timeWork experience placementLocal area- ...clinical research activities at the study and site levels, including documentation, vendor... ..., and project management tasks. Develop trial timelines, enrollment projections, and... ...support trial execution, propogating plans for monitoring, recruitment, risk mitigation, and...Website
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