Senior Clinical Research Associate - On-Site Monitoring Expert
IQVIA
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 a Bachelor's degree and at least 2 years of experience in on-site monitoring. Strong knowledge of clinical research regulations and GCP guidelines is required. Competitive salary range is provided, along with additional benefits. #J-18808-Ljbffr IQVIA
- IQVIA LLC is seeking a Sr. Clinical Research Associate to monitor and manage oncology clinical trial sites in Overland Park, KS. This role involves key responsibilities such as conducting site monitoring visits, ensuring compliance with regulations, and managing subject...SeniorWebsite
- ...Argentina is looking for a CRA 2 with at least 1.5 years of on-site oncology monitoring experience. The successful candidate will perform site... ...and manage study progress while ensuring adherence to Good Clinical Practice (GCP) and International Conference on Harmonization...SeniorWebsiteFull time
- 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...SeniorWebsiteRemote job
$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 care...Website$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'...Website$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 a...WebsiteFull timeWork at office- A leading clinical research organization is seeking a Clinical Research Associate dedicated to supporting clinical trials. The ideal... ...should have 1-2 years of onsite monitoring experience, a bachelor's... ...requirements. The role involves site monitoring visits, ensuring compliance...Website
$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...WebsiteWork at office- ...Shawnee, Kansas, is seeking an experienced Clinical Research Associate to join its team. The ideal candidate... ...have over 8 years of clinical trial monitoring experience within an Animal Health... ..., building rapport with study site staff, and managing adverse event documentation...SeniorWebsite
- ...divh2Senior Clinical Research Associate, Early Clinical Development/h2pOverland Park, United... ...Clinical Development is hiring for a Senior CRA 1. Ideal candidates will... ..., you will be responsible for monitoring and managing clinical sites to ensure compliance with study...SeniorWebsiteFull time
$71.9k - $189k
...: Posted Todayjob requisition id: R1541483Job Overview: Join our dynamic team as a Clinical Research Associate! You’ll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements. Be...SeniorWebsiteFull timePart timeWork at officeLocal areaImmediate startWorldwide$115k - $135k
...Altasciences. About The Role The Manager, Clinical Monitoring Services is responsible for the day-to-... ...monitoring metrics such as number of site visits performed, utilization, and... ...period of 3 years is preferable in clinical research monitoring or equivalent experience....SeniorWebsiteHourly payPermanent employmentContract workWork at officeRemote work$105k - $125k
A biopharmaceutical company is looking for experienced Ophthalmology Clinical Research Associates (CRAs) to oversee study site monitoring. This role involves leading clinical trials, ensuring adherence to study protocols, and reporting Serious Adverse Events (SAEs). The...SeniorWebsiteRemote workFlexible hours- A prominent healthcare organization is seeking a remote Clinical Research Associate (CRA) to manage clinical site monitoring services for various projects. The role requires fluency in both English and French, with a focus on site recruitment, oversight of project budgets...SeniorWebsiteRemote job
- ...divh2Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions/h2pICON is a global... ...will have cardiovascular medical device monitoring experience- however, cardiovascular/... ...risks and identify issues at sites and implement effective solutions promptly...SeniorWebsite
- ...treatments that benefit patients worldwide. Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All... ...have cardiovascular medical device monitoring experience—however, cardiovascular/... ...risks and identify issues at sites and implement effective solutions promptly...SeniorWebsiteWorldwide
$101.6k - $169.3k
...divh2Sr. Clinical Research Associate, IQVIA/h2pOverland Park, United States of America | Full time... ...based | R1537588/ppIQVIA is hiring Senior Clinical Research Associate 1 with... ...respiratory:/ppJob Overview:/ppPerform monitoring and site management work to ensure that...SeniorWebsiteFull timePart timeLocal areaImmediate startWorldwide$101.6k - $169.3k
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-... ..., dermatology, or respiratory: Job Overview Perform monitoring and site management work to ensure that sites are conducting the...SeniorWebsiteFull timePart timeLocal areaImmediate start$101.6k - $169.3k
A leading clinical research organization is seeking a Senior Clinical Research Associate 1 in Kansas City, MO. The role involves monitoring clinical trials and ensuring compliance with regulations... ...degree and at least 2 years of on-site monitoring experience....SeniorWebsite- A leading clinical research organization is seeking a Senior Clinical Research Associate in Kansas City, Missouri. This role involves overseeing clinical trial activities,... ...adherence to protocols and compliance, and managing site performance. The ideal candidate will have an...SeniorWebsite
- ...Senior CRA / CRA II - Home-Based (US) ICON plc... ...healthcare intelligence and clinical research organization. We're... ...on clinical trial monitoring tasks requiring... ...Monitoring clinical trial sites to ensure adherence to... ...a Clinical Research Associate, with a strong understanding...SeniorWebsiteRemote jobWork from homeFlexible 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... ...in Study Start-Up and at least 6 months of on-site or in-house monitoring experience. Candidates can be located anywhere in the...WebsiteFull timePart timeLocal areaImmediate startWorldwide- Clinical Research Associate - Multi TA ICON plc is a world-leading healthcare intelligence and clinical research organization. We... ...the study lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements...WebsiteFlexible hours
$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...WebsiteFull timePart timeLocal areaImmediate startWorldwide$66.8k - $120k
...Conditions Office Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of... ...to perform and coordinate all aspects of the clinical monitoring and site management process. As a Clinical Research Associate (Level...WebsiteTemporary workWork at officeRemote workHome officeNight shift$78k - $130k
...in English and French. Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include... ...collaborative relationships with stakeholders. Monitoring - Subject Expert Act as subject matter expert, mentor, coach and/or provide...SeniorWebsiteRemote workWork from home$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...Website$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...WebsiteWork at office- ...Position Type: Transportation/Bus Monitor Date Posted: 6/1/2025 Location: Transportation Facility Job Description... ...Director of Transportation, Bus Driver while en route. Site: Shawnee Public Schools - all sites Qualifications...WebsiteContract work
$71.9k - $182k
...divh2Clinical Research Associate (CRA) 2 Level/h2pIQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal... ...will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular... .../ppPerform monitoring and site management work to ensure that...WebsiteFull timePart timeLocal areaImmediate startWorldwide
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