Travel-Ready Clinical Research Associate - Trial Monitoring
ICON Strategic Solutions
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 are university-level qualifications, knowledge of ICH-GCP, strong English communication, and willingness to travel ~60%. ICON offers comprehensive benefits and a diverse, inclusive culture. #J-18808-Ljbffr ICON Strategic Solutions
- ...healthcare intelligence and clinical research organization. This Clinical Research Associate II role in the Midwest... ...analyzing clinical trials, interpreting complex... ...treatments. You will monitor sites, ensure protocol... ...across studies, with travel up to about 60% as needed...Travel
$110.52k - $138.15k
Senior Clinical Research Associate - Oncology Phase I - ChicagoICON is... ...site management and monitoring activities throughout the clinical trial lifecycle. This Sr. CRA... ..., and inspection readiness at the clinical investigative... ...preferred Willing to travel up to 50% Employment...TravelFull timeInterim roleLocal areaRemote work- ...seeking a qualified candidate to oversee site management for clinical research programs. The role emphasizes ensuring compliance with ICH-GCP... ...project coordination, data accuracy, and the ability to travel domestically and internationally (approximately 65-75%). #J-...Travel
- ICON plc in Chicago is seeking a Clinical Research Associate to serve as the primary liaison between investigational... ...documentation in CTMS and eTMF, monitor patient safety, and support site... ...-site monitoring experience, and can travel up to 50% across #J-18808-Ljbffr...Travel
$96.2k - $151.4k
...all phases of a clinical research study, taking overall... ...as SME for monitoring processes and systems... ...phases of the trial. Performs clinical... ...Plan and associated documents. Gains... ...to achieve Site Ready. Participates... ...capabilities. Extent of Travel Ability to...TravelFor contractorsLocal areaRemote work2 days per week3 days per week- ...Experienced Clinical Research Associate - Sponsor Dedicated Syneos... ...initiation, interim monitoring, site management... ...of the ISF with the Trial Master File (TMF). Ensures... ...level towards audit readiness standards and... ...to manage required travel of up to 75% on a regular...TravelContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Clinical Research Associate (Start up) - Cross Therapeutic Area - Illinois... ...Works on multiple trials within the Cross... ...project milestones. Monitor, report on, and analyze... ...documentation to ensure readiness for inspections.... ...memberships, subsidized travel passes, health...TravelLocal areaRemote workWork visaFlexible hours
$66.8k - $125k
...Office Join Us as a Clinical Research Associate (Level II) - Make an... ...2,700 clinical trials across 100+ countries... ...of the clinical monitoring and site management... ...You will ensure audit readiness and develop collaborative... ...• 1-2 years of traveling on-site monitoring experience...TravelFull timeTemporary workWork at officeRemote workHome officeNight shift- ...A Senior Clinical Research Associate (Sr. CRA) is responsible for: Conducting monitoring activities at assigned clinical trial site(s) Verifying the adequacy... ...studies and sites Travels to research sites to... ...to ensure inspection readiness at all times Maintains...TravelFull timeFixed term contractInterim roleLocal areaWork from home
- Senior Clinical Research Associate - Oncology Phase I - Chicago ICON plc... ...site management and monitoring activities throughout the clinical trial lifecycle. This Sr.... ...state of inspection readiness Act as the primary contactandfacilitateefficient... ...preferred Willing to travel up to 50% What ICON...TravelInterim roleLocal areaRemote workFlexible hours
- ...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... ...visits, maintain inspection readiness, and collaborate with trial teams. Travel up to 50% and mentoring junior...Travel
$65k - $80k
...costs in peer-reviewed cancer research grants, and $24 million in... ...fundraising, data analytics, clinical trials management, and community... ...Summary Manages, facilitates, and monitors daily clinical research and... ...teams and assists in audit readiness and preparation....Work experience placementWork at officeLocal areaRemote work- Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All RegionsICON... ...cardiovascular medical device monitoring experience- however,... ...sites.Well-versed in clinical trial management. They are rigorous... ...to cover up to 65% regional travel.Employment with ICON is...TravelFull time
- Clinical Research AssociateICON is a global healthcare intelligence... ...and analyse clinical trials, interpreting complex... ...to clinical trial monitoring activities, taking... ...a Clinical Research Associate.In-depth knowledge of... ...environment.Willingness to travel as required (...TravelFull time
$91.34k - $114.17k
Clinical Research Associate - Oncology - ChicagoICON is a global healthcare intelligence... ..., initiation, routine monitoring, and close-outEnsure site... ...monitoring Oncology clinical trials required, preferably heme/... ...playerWilling and able to travel up to 50% for on-site monitoring...TravelFull timeLocal area$120k - $145k
...Companies is actively seeking Clinical Research Associates to join a toptier CRO with... ...remote but does require travel 60-80% of the time... ...and sites, ensuring clinical trials follow protocols, protect patients... ...with the team to ensure monitoring activities meet study...TravelRemote work- ...Team in Cincinnati, Ohio!The Clinical Research Associate position offers an exciting... ...the research field, travel the US, and be part of a team... ...qualification, initiation, monitoring, and closeout visits at research... ...our integrated Clinical Trial Management System to identify...TravelContract workWork experience placementWork at officeRemote workWork from home
- ICON Strategic Solutions is seeking a Clinical Research Associate for our Chicago office. This role involves serving... ...equivalent, at least 2 years of on-site monitoring experience, and a strong background in Oncology clinical trials. ICON offers a competitive salary and...Work at office
$75.48k - $94.35k
...Clinical Research Associate- Central/Mid-WestICON is a global healthcare intelligence... ...contribute to our clinical trial operations function,... ...delivering clinical trial monitoring work to a high standard, working... ...timely mannerWillingness to travel as required (approximately...Travel$91.34k - $114.17k
...Clinical Research Associate - Oncology - ChicagoICON plc is a world-leading healthcare... ..., initiation, routine monitoring, and close-outEnsure site compliance... ...Oncology clinical trials required, preferably heme/oncProficient... ...playerWilling and able to travel up to 50% for on-site...TravelWork experience placementLocal area- ...in Cincinnati, Ohio! The Clinical Research Associate position offers an exciting... ...the research field, travel the US, and be part of a team... ...qualification, initiation, monitoring, and closeout visits at research... ...our integrated Clinical Trial Management System to identify...TravelContract workWork experience placementWork at officeRemote workWork from homeHome officeFlexible hours
- ...Clinical Research Associate- Central/Mid-West ICON plc is a world-leading healthcare... ...contribute to our clinical trial operations function,... ...delivering clinical trial monitoring work to a high standard, working... ...manner Willingness to travel as required (approximately...TravelFlexible hours
- ...Clinical Research Associate- Mid-West ICON plc is a world-leading healthcare intelligence... ...and analyse clinical trials, interpreting complex... ...contribute to clinical trial monitoring activities, taking responsibility... .... Willingness to travel as required (approximately...TravelFlexible hours
- Job SummaryClinical Research Coordinators... ...based opportunity for clinical research professionals... ...Clinical Research Associate (CRA) openings... ...to earn a generous travel bonus, in addition... ..., initiation, monitoring, and closeout visits... ...integrated Clinical Trial Management System...TravelContract workWork at officeRemote workWork from home
$100k - $120k
...currently seeking aClinical Research Associate (CRA) for an... ...Chicago, Illinois (IL).The Clinical Research Associate (... ...in ongoing Clinical Trials throughout the... ...and perform all site monitoring activities across multiple... ...trial documentation Some travel required once travel...TravelRemote work- ...selection, initiation, routine monitoring, and close-out visits in... ...issues, escalating risks to the Clinical Team Lead/PM as appropriate Review... ...to audit/inspection readiness at site and study level Liaise... ...company structure Willingness to travel 30% for on-site visits (...TravelRemote work
- 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
- ...Senior Clinical Research Associate - Oncology Phase I - Chicago ICON... ...site management and monitoring activities throughout the clinical trial lifecycle. This Sr. CRA... ..., and inspection readiness at the clinical investigative... ...~ Willing to travel up to 50% What ICON...TravelRemote jobInterim roleLocal areaFlexible hours
- ...Clinical Research Coordinators Wanted At Medpace Become... ...fill Clinical Research Associate (CRA) openings with Medpace... ...to earn a generous travel bonus, in addition to... ..., initiation, monitoring, and closeout visits... ...integrated Clinical Trial Management System to...TravelContract workWork at officeRemote workWork from homeHome officeFlexible hours
- The 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...
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