Senior Clinical Trial Monitoring Lead
$101.6k - $169.3kIQVIA
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. Applicants should have a Bachelor's degree and at least 2 years of on-site monitoring experience. Competitive salary range is $101,600-$169,300 based on qualifications and other factors. This position offers opportunities for growth in a dynamic environment focused on impactful research. #J-18808-Ljbffr
$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...Senior- ...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...Senior
- ...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...SeniorRemote work
- ...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...Senior
- ...A leading clinical research organization is seeking a Senior Clinical Research Associate in Kansas City, Missouri. This role involves overseeing clinical trial activities, ensuring adherence to protocols and compliance, and managing site performance. The ideal candidate...Senior
$115k - $135k
...and together We Are Altasciences. About The Role The Manager, Clinical Monitoring Services is responsible for the day-to-day management of... ...the oversight of clinical monitoring activities for assigned trials. What You'll Do Here Leadership & Operational Excellence Provide...SeniorHourly payPermanent employmentContract workWork at officeRemote work- ...Senior CRA ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive... ...overseeing and managing clinical trial activities to ensure they are... .... What You Will Be Doing: Monitoring clinical trial sites to ensure...SeniorFlexible hours
$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...SeniorRemote workFlexible hours- ...looking for a CRA 2 with at least 1.5 years of on-site oncology monitoring experience. The successful candidate will perform site... ...visits and manage study progress while ensuring adherence to Good Clinical Practice (GCP) and International Conference on Harmonization (...SeniorFull time
- ...ICON is looking for a Clinical Research Associate in St. Louis who will play an essential role in clinical trials, ensuring protocol compliance and data integrity. The successful... ...-related field and at least 9 months of monitoring experience are essential. ICON values...
- Parsons is searching for a dedicated Property Administrator, Senior in Kansas City, Missouri. This role involves monitoring compliance and accountability of assets, implementing property processes, and ensuring operational readiness of materials and equipment. The ideal...SeniorFlexible hours
- ...A leading healthcare organization in Kansas City is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities ensuring compliance with protocols and quality standards. The ideal candidate will possess an advanced degree, extensive CRA experience...Senior
$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...Work 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...- ...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...
$71.9k - $189k
...the job is located. Perform monitoring and site management work to ensure... ...scope of work and Good Clinical Practice. • Work with sites to... ...available for filing in the Trial Master File (TMF) and verify... ...managers, and clients. IQVIA is a leading global provider of clinical...Full timePart timeLocal areaWorldwide$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...$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...Full timeWork at office- ...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...
$71.9k - $119.9k
...A global clinical research organization is seeking a Clinical Research Associate I (CRA I) to conduct monitoring visits and support clinical research studies. The role requires a bachelor... ...I will ensure compliance with clinical trial protocols and maintain communication...$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...$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$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...Flexible hours$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$71.9k - $119.9k
A global clinical research organization is seeking a Clinical Research Associate I (CRA I) to conduct monitoring visits and support clinical research studies. The role requires a bachelor... ...I will ensure compliance with clinical trial protocols and maintain communication...- ...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...SeniorRemote work
$100k - $215k
...portfolio. This position can be filled at the Executive Underwriter or AVP Underwriting Director level. Responsibilities include monitoring projects, analyzing risk, and building customer relationships. Candidates should have strong Workers Compensation expertise, excellent...Senior- STO Building Group is hiring a Senior Safety Coordinator in Kansas City, Missouri. This role involves upholding environmental, safety... ...health standards at construction sites. Responsibilities include monitoring conditions, ensuring compliance with OSHA standards, and...Senior
$89k - $148k
...A reputable healthcare firm in the United States seeks a Medical Writer to lead writing projects for clinical research. Ideal candidates will have 7-9 years of experience, expertise in regulatory documents like clinical study reports, and a degree in a relevant field....Senior$87.2k - $169.3k
...IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase 1 experience across a variety... ...the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance...SeniorFull timePart time
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