CRA I: On-Site Clinical Trial Monitor & Liaison
IQVIA
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 effectively. The ideal candidate should have a Bachelor's degree in life sciences or healthcare and at least 1.5 years of on-site monitoring experience. Join us in making a direct impact on clinical research and improving patient outcomes. #J-18808-Ljbffr IQVIA
- 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...WebsiteRemote work
- ...healthcare intelligence and clinical research organization, is... ...II in the Mid-West. As a CRA II at ICON, you will design and analyse clinical trials, interpret complex medical... ...therapies. Key duties include site qualification, initiation, monitoring, and close-out visits,...Website
- CRA Monitor (Midwest + East Coast) job at Planet Group. Chicago, IL. The Clinical Research Associate (CRA) is primarily responsible for ensuring... ...the rights & wellbeing of trial participants are protected... ...between the Investigational Sites and Sponsor. Key responsibility...WebsiteLocal areaRemote work
- ICON Clinical Research in Chicago is seeking a Clinical Research Associate... ...between investigational sites and the sponsor.... ...compliance with regulations, and monitoring patient safety. The ideal candidate... ...and familiarity with oncology trials. ICON offers a competitive salary...Website
- 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 with...Website
- Barrington James is seeking a Senior 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...Website
- 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's...Website
- Merck in the United States seeks an experienced Clinical Research Associate with ophthalmology expertise to oversee site performance and regulatory compliance for... ...phases. The role includes expanding territory, monitoring visits, site selection input, and collaboration...WebsiteRemote jobLocal area
$190k - $210k
...Regional Medical Science Liaison, Central Ideal location should... ...states, and collaborate to support clinical research activities. Who is... ...completed Phase 1 clinical trials. Under a recently announced... ...development activities through site identification and...WebsiteLocal areaNight shift- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization... ..., and interpretation of clinical trials. This includes serving as the... ...point of contact for investigative sites and sponsors, and providing real-time...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
- ...Strategic Solutions is seeking a Clinical Research Associate for our... ...contact between investigational sites and sponsors, managing site... ..., at least 2 years of on-site monitoring experience, and a strong background in Oncology clinical trials. ICON offers a competitive salary...WebsiteWork at office
- ICON plc in Chicago is seeking a Clinical Research Associate to serve as the primary liaison between investigational sites and sponsors, conducting site visits and ensuring ICH... ...will manage documentation in CTMS and eTMF, monitor patient safety, and support site staff...Website
$71.9k - $189k
IQVIA 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...WebsiteFull time- ...world-leading healthcare intelligence and clinical research organization. This Clinical... ...involves designing and analyzing clinical trials, interpreting complex medical data, and... ...contributing to innovative treatments. You will monitor sites, ensure protocol compliance, and work...Website
- ...Florida, California, NY, ColoradoThe role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's...WebsiteFull timeRemote work
- OnPoint Clinical Staffing Services is seeking a Clinical Research Monitor based in Chicago, Illinois. Candidates should have over 5 years of experience in clinical... ...Pharmaceutical environment. The role involves all aspects of site monitoring, presentations at Investigator...Website
$87.2k - $169.3k
...Team That’s Advancing Clinical ResearchWe’re looking for... ...Research Associate (CRA) to join our team and play... ...high-quality clinical trials. In this role, you’ll partner... ...with investigative sites and cross-functional... ...DoLead and execute site monitoring visits (selection, initiation...WebsiteFull timePart timeImmediate startWorldwide- ...wanted at Medpace! Become a CRA and join our growing team... ...-based opportunity for clinical research professionals... ...qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved... ...our integrated Clinical Trial Management System to...WebsiteContract workWork at officeRemote workWork from home
$96.2k - $151.4k
...assigned protocols and sites in a country.Under the oversight of the CRA-Manager the person ensures... ...all phases of a clinical research study, taking overall... ...workstreams as SME for monitoring processes andSystems.Responsibilities... ...all phases of the trial.Performs clinical study...WebsiteFull timeFor contractorsLocal areaRemote workFlexible hours2 days per week3 days per week$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
...scale? As a Precision Medicine Liaison, you will play a critical... ...genomic insights into everyday clinical care. Operating at the intersection... ...diagnostic, prognostic, and monitoring workflow initiatives across... ...diagnostic workflows across sites, departments, and service...WebsiteFull timeLocal areaRemote work- ...DescriptionThe EVERSANA Medical Science Liaison/Senior Medical Science Liaison... ...professionals and leaders in clinical, scientific, value-based care... ...clinical protocols, clinical trials outcomes and related... ...collaborate with R&D Team to support sites and investigators...WebsiteLocal area
- ...DescriptionThe EVERSANA Medical Science Liaison/Senior Medical Science Liaison... ...professionals and leaders in clinical, scientific, value-based care... ...clinical protocols, clinical trials outcomes and related... ...Collaborate with R&D Team to support sites and investigators...WebsiteLocal areaNight shift
$186k - $310k
...the Oncology Medical Science Liaison (MSL) role offers a highly impactful... ...MSL, you will bring strong clinical and therapeutic expertise and... ..., you will support clinical trials by facilitating relevant medical... ...the vacancies posted on this site. All employment businesses/agencies...WebsiteFull timeLocal area$162.8k - $203.5k
...position of Medical Science Liaison. The Medical Science... ...information to aid the clinical and marketing teams in... ..., evaluate and monitor investigator-sponsored... ...investigators for corporate trials. Assist the clinical trials... ...role with periodic on-site meetings in office. Must...WebsiteFull timeWork at officeLocal areaRemote workFlexible hours$163k - $245k
...hands.Summary of roleThe Medical Science Liaison (MSL) is a key member of Global Medical Affairs, communicating scientific, clinical and technical information within the medical... ..., medical imaging trends, clinical trials and scientific activities within the oncology...Full timeLocal areaRemote work- 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
$170.32k - $212.9k
...Your ImpactThe Thought Leader Liaison (TLL) serves as a strategic, field... ...at both Teva HQ and off-site locations throughout the US. Occasional... ...and speaker preparation.Monitor speaker utilization and... ...preferredStrong scientific and clinical acumen with the ability to interpret...WebsiteLocal areaWorldwideFlexible hoursWeekend work- 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
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