Clinical Research Associate - Onsite Monitoring
IQVIA
A leading clinical research organization is seeking a Clinical Research Associate dedicated to supporting clinical trials. The ideal candidate should have 1-2 years of onsite monitoring experience, a bachelor's degree in a scientific discipline, and a strong understanding of regulatory requirements. The role involves site monitoring visits, ensuring compliance with study protocols, and managing project-related communications. Competitive pay range is offered, along with opportunities for growth and development in the clinical research field. #J-18808-Ljbffr
$71.9k - $169.3k
...A leading health data science company is seeking a Clinical Research Associate (CRA) to manage monitoring and site management tasks. Candidates should have 1-2 years of onsite experience, particularly in Cardiovascular, Oncology, or Neurology. The role involves regulatory...SuggestedFlexible hours$47.4k - $169.3k
...IQVIA Argentina is looking for a Clinical Research Associate in Overland Park, United States. This full-time position involves performing site monitoring and management to ensure compliance with study protocols and regulatory guidelines. The ideal candidate will have...SuggestedFull timeWork at office$71.9k - $169.3k
...IQVIA LLC seeks a Clinical Research Associate in Overland Park, KS. This role involves conducting site monitoring and management to ensure compliance with study protocols and relevant regulations. Candidates should possess a Bachelor's Degree, at least a year of on-site...SuggestedWork at office$71.9k - $169.3k
...IQVIA is seeking a Clinical Research Associate in Overland Park, KS to perform monitoring and site management. The role includes ensuring that sites comply with regulations and study protocols while managing site-related data. The ideal candidate should hold a Bachelor...Suggested$87.2k - $182k
...IQVIA seeks a Monitoring Specialist in Overland Park, Kansas. This role involves performing monitoring and site management tasks to ensure compliance with study protocols and regulations. Candidates should have a Bachelor’s Degree in a scientific discipline or health...Suggested$71.9k - $189k
...IQVIA is looking for a Site Monitor in Overland Park, Kansas. The role involves site management and monitoring to ensure compliance with protocols and regulations. Candidates should have at least 2 years of monitoring experience and preferably a Bachelor's Degree in a...Work at office- ...A leading clinical research organization is seeking a Senior Clinical Research Associate 1 in Overland Park, Kansas. This role involves monitoring clinical study sites, ensuring compliance with protocols, and managing site relationships. The ideal candidate will have...
$101.6k - $169.3k
...IQVIA in Lenexa, Kansas, is hiring a Senior Clinical Research Associate 1 to manage site monitoring and ensure protocol compliance. The role requires a minimum of 2 years of on-site monitoring experience and a Bachelor's Degree in a scientific discipline or healthcare....- ...Syneos Health/inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate in the United States, Missouri. The role involves performing site qualifications, monitoring activities, and ensuring compliance with regulatory guidelines. Candidates should...Remote work
$71.9k - $189k
...country where the job is located. Perform monitoring and site management work to ensure that... ...with contracted scope of work and Good Clinical Practice. • Work with sites to adapt, drive... ...skill in applying, applicable clinical research regulatory requirements. • i.e., Good...Full timePart timeLocal areaWorldwide$71.9k - $169.3k
...IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic, Oncology, and/or Neurology. Candidates can be located anywhere in the US. Job...Full timePart timeLocal area$71.9k - $189k
IQVIA Argentina is seeking a Clinical Research Associate based in Kansas City, USA. This full-time role involves conducting site monitoring visits according to Good Clinical Practice, managing study progress, and ensuring compliance with regulations. The ideal candidate...Full timeWork at office$69.8k - $226.8k
...Job Overview Join our team as a Clinical Research Site Manager, where you’ll play a crucial role in ensuring our study sites operate seamlessly... ..., and sponsor requirements. Essential Functions Site Monitoring: Conduct selection, initiation, monitoring, and close-out visits...Full timePart timeLocal areaImmediate startWorldwide$71.9k - $169.3k
...Clinical Research Associate - Sponsor Dedicated Location: Overland Park, KS. Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations...Local area$71.9k - $169.3k
...IQVIA Argentina is hiring a Clinical Research Associate in Overland Park, Kansas. The role includes monitoring and managing clinical trial sites to ensure compliance with protocols and regulations. Ideal candidates should have 1-2 years of experience in clinical research...- ...Clinical Research Associate - St Louis/Kansas City/Ohio ICON plc is a world-leading healthcare intelligence... ...site qualification, initiation, monitoring, and close-out visits for clinical trials... ...-related field. Minimum of 9 months onsite monitoring experience as a Clinical...Flexible hours
$71.9k - $145.3k
...Study Start-Up Clinical Research Associate IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams... ...Study Start-Up and at least 6 months of on-site or in-house monitoring experience. Candidates can be located anywhere in the...Full timePart timeLocal areaImmediate startWorldwide- Clinical Research Associate - Multi TA ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud... ...throughout the study lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study...Flexible hours
$87.2k - $169.3k
...IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will... ...Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key... ...position, you will be responsible for monitoring and managing clinical sites to ensure...Full timePart time- ...Argenta, located in Shawnee, Kansas, is seeking an experienced Clinical Research Associate to join its team. The ideal candidate will have over 8 years of clinical trial monitoring experience within an Animal Health pharmaceutical company and proven expertise in GCP compliance...
$66.8k - $120k
...Conditions Office Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation... ...opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Clinical Research...Temporary workWork at officeRemote workHome officeNight shift- ...divh2Clinical Research Associate - Sponsor Dedicated/h2pOverland Park, United States of America... ...based | R1541452/ppJob Overview: Perform monitoring and site management work to ensure... ...with contracted scope of work and Good Clinical Practice./liliWork with sites to adapt...Full timeLocal area
- ...divh2Clinical Research Associate, Full Service/h2pOverland Park, United States of America | Full... ...| R1497311/ppJob Overview Perform monitoring and site management work to ensure that... ...and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference...Full timeLocal area
$80k - $114k
...Credit Monitoring Analyst III The Credit Monitoring Analyst III supports the commercial... ...Reliable and predictable attendance; both onsite and remote. Education & Experience... ...assistance program. In addition, eligible associates may take advantage of pre-tax health savings...Temporary workWork at officeLocal areaRemote workFlexible hours$71.9k - $169.3k
...IQVIA in Overland Park, Kansas is seeking a Site Monitor to perform monitoring and site management for clinical studies. The role includes ensuring compliance with study protocols, conducting site visits, and managing documentation. Candidates should have a Bachelor's...- ...register to view more details about this job. Contractor, Monitoring, Evaluation and Learning Reports To: Director, Monitoring,... ...related field. Prior experience with data cleaning, analysis, or research is beneficial. Skills Proficiency in Microsoft Excel (...Temporary workFor contractorsLive inRemote work
- ...A leading biotech firm in Overland Park is hiring a Clinical Research Associate I (CRA I) to support clinical studies through site monitoring and management. The CRA I is responsible for ensuring compliance with protocols and regulations, conducting various monitoring...
- ...Position Type: Transportation/Bus Monitor Date Posted: 6/1/2025 Location: Transportation Facility Job Description SHAWNEE PUBLIC SCHOOLS Job Title: Bus Monitor Reports To: Director of Transportation, Bus Driver while en route...Contract work
$87.2k - $182k
...IQVIA LLC is seeking a Clinical Research Associate to conduct site monitoring visits, manage study progress, and ensure compliance with regulations. Qualified candidates should have a Bachelor’s Degree in a scientific discipline or healthcare and at least 1.5 years of...Work at office$17 per hour
...Lunch Monitor - Marion Elementary Job ID: 5544460 Application Deadline: Posted until filled Posted: Feb 18, 2026 6:00 AM (UTC) Starting Date: To Be Determined Job Description 2025-2026SCHOOL YEAR (Posted: 02/18/2026) POSITION: Lunch Monitor (Cafeteria/Recess Monitor) LOCATION...Hourly payPart timeMonday to Friday
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