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
$87.2k - $169.3k
...IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase 1 experience... ...a dedicated Clinical Research Associate (CRA) to join our team and... ...you will be responsible for monitoring and managing clinical sites to ensure compliance with study...SeniorWebsiteFull timePart time$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$101.6k - $169.3k
IQVIA Argentina in Overland Park is seeking a Site Manager to perform monitoring and site management tasks in clinical research. Ideal candidates should have a Bachelor's degree in a scientific or healthcare field and at least 2 years of on-site monitoring experience. This...Website- 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
- Join IQVIA, where we value integrity and diversity, and contribute to impactful clinical studies that enhance patient care. #J-18808-Ljbffr IQVIAWebsite
$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$71.9k - $189k
Job 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 at the forefront of groundbreaking cancer...SeniorWebsiteWork at officeLocal area$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$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 work
$101.6k - $169.3k
...IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP... ...NASH, dermatology, or respiratory: Job Overview Perform monitoring and site management work to ensure that sites are conducting...SeniorWebsiteFull timePart timeLocal areaImmediate start$101.6k - $169.3k
...Senior Clinical Research Associate 1 IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular... ..., or respiratory: Job Overview: Perform monitoring and site management work to ensure that sites are conducting the...SeniorWebsiteFull timePart timeLocal areaImmediate startWorldwide- Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions ICON plc is a world-leading healthcare... ...have cardiovascular medical device monitoring experience- however, cardiovascular/... ...risks and identify issues at sites and implement effective solutions...SeniorWebsiteFlexible hours
- ...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
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
$233k - $315k
Department: 106750 Clinical Development Location: San Diego, USA- Remote Be a part... ...rare patients. Position Summary The Senior Director, Medical Monitor & Safety Physician is a clinical and... ...‑face work with colleagues and/or on‑site in San Diego. No role is expected to...SeniorWebsiteTemporary workRemote work- ...Clinical Research Associate 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 and guidelines, and sponsor requirements. Essential Functions...WebsiteLocal area
$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- ...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
$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- ...Superintendent in Overland Park, KS to manage large podium multi-family construction projects. You will be responsible for all facets of on-site management including safety, quality, and budget adherence. The ideal candidate will have extensive experience running projects...SeniorWebsitePermanent employment
- IQVIA is seeking Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates are based in the... ...States and have 1-2 years of onsite monitoring experience with expertise in areas... ...role involves performing monitoring and site management work to ensure compliance...Website
$71.9k - $189k
IQVIA Argentina seeks a Clinical Research Associate in Overland Park, Kansas. In this role, you will conduct site monitoring, ensuring adherence to study protocols and regulatory requirements. Ideal candidates should have at least 1 year of on-site monitoring experience...Website- PNC is hiring a Loan Support Analyst Senior in Overland Park, Kansas. The role involves covenant monitoring and testing of commercial real estate loans, ensuring compliance with loan documents and communicating with borrowers on financial results. The ideal candidate will...Senior
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