Clinical Research Site Manager: Monitoring & Study Delivery
IQVIA
A leading global clinical research organization is seeking a Clinical Research Site Manager in Overland Park, Kansas. You will conduct site monitoring, manage recruitment plans, and mentor clinical staff to ensure study sites adhere to all protocols. The ideal candidate has a BS degree in a scientific discipline, at least 2.5 years of on-site monitoring experience, and strong communication and organizational skills. A competitive salary and benefits package are offered. #J-18808-Ljbffr
$71.9k - $169.3k
...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... ...role involves regulatory compliance, evaluation of study sites, and effective communication with team members...SuggestedFlexible hours$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's degree and 6 months... ...with investigative sites. The compensation package ranges...Suggested$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's degree and 6 months... ...with investigative sites. The compensation package ranges...Suggested$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...SuggestedWork 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...Suggested
$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...$93.1k - $232.8k
...Overview Senior Clinical Leads are an... ...clinical trial delivery, leading and... ...multi-regional studies to meet contractual... ...plan. Manage clinical risks... ...will be measured, monitoring and overseeing... ...• May attend site visits as applicable... ...years clinical research/monitoring experience...Full timeContract workPart timeWork at officeLocal areaImmediate startWorldwide- Senior Clinical Trial Manager ICON plc is a world-leading... ...and clinical research organization. We’re... ...trial management delivery, resolving issues,... ...Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring... ...our careers site to read more about...Flexible 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 a...Full timeWork 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...$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- ...A leading clinical research organization is seeking a Clinical Research... ...should have 1-2 years of onsite monitoring experience, a bachelor's... .... The role involves site monitoring visits, ensuring compliance with study protocols, and managing project-related communications...
$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...$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... ...successful candidate will perform site visits, manage study progress, and maintain communication with sites. In...- ...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...
- ...ICON is looking for a Clinical Research Associate in St. Louis who will play an essential... ...will conduct visits, prepare study documentation, and collaborate with site staff. A Bachelor’s degree in a... ...field and at least 9 months of monitoring experience are essential. ICON...
$115k - $135k
...Altasciences. About The Role The Manager, Clinical Monitoring Services is responsible for... ...Clinical Practice, and study-specific requirements.... ...metrics such as number of site visits performed, utilization... ...is preferable in clinical research monitoring or equivalent experience...Hourly payPermanent employmentContract workWork at officeRemote work- ...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...
$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$62.26k - $74.71k
...711.00 / Year Job Category: Clinical Research, Clinical Trials Employee Type... ...Degree: High school Manage Others: No Contact information... ...role in the conduct of the study. Works closely with the clinical... ...patients, performing study visits, monitoring patient’s study progress,...Work at officeShift work- ...Clinical Research Coordinator Department: Operations Employment... ...is a growing multi‑site, multi‑phase clinical... ...across Phase I‑IV studies and several therapeutic... ...as needed Conducting monitoring visits and resolving... ...co‑workers, subjects, managers and external customers...Full timeTemporary work
- ...Senior Clinical Research Coordinator - Cancer Center page is loaded## Senior... ...in the overall clinical study coordination of clinical research... ...Research Coordinator will manage assigned clinical research... ...scope of practice.* Facilitate monitoring visits, reviews and audits....Full timeContract workWork experience placement
- ...Clinical Research Coordinator - Cancer Center page is loaded## Clinical Research... ...in the overall clinical study coordination of clinical research. This position manages assigned clinical research studies... ...analysis of clinical research data. Monitors participants' progress...Full timeWork experience placement
- ...Clinical Research Coordinator Alcanza is a growing multi-site, multi-phase clinical research company with... ...presence across Phase I-IV studies and several... ...needed; Conducting monitoring visits and resolves issues... ...co-workers, subjects, managers and external customers...Full timeTemporary work
$71.9k - $189k
...the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data... ...scope of work and Good Clinical Practice. • Work with sites... ...applying, applicable clinical research regulatory requirements. • i...Full timePart timeLocal areaWorldwide$114k - $210.9k
...Experienced Clinical Trial Manager - Full-Service Job Responsibilities... ...Responsible for site management oversight, clinical monitoring and central... ...). Reviews the study scope of work,... ...to coordinate delivery handoffs and meet... ...conduct of a clinical research project....Contract workFlexible hours- ...Diseases ----- CCR Position Title: Clinical Research Coordinator- Cardiology Job... ...in the overall clinical study coordination of clinical... ...visits in the Clinical Trials Management System, study expenditures and... ...and participate in study monitoring visits, reviews and audits....Full timeWork experience placement
- COLLATERAL MONITORING MANAGER SUMMARY This position is responsible for supervising and analyzing... ...Create and run queries; conduct industry research and analysis. Prepare forms, reports,... ...university or institution with a major area of study in accounting, finance, business...Work experience placement
- ...Commercial LLC is seeking an Experienced Clinical Research Associate in the United States,... .... The role involves performing site qualifications, monitoring activities, and ensuring compliance... ...accelerating therapies, with a requirement to manage travel of up to 75%. A range of...Remote work
- ...Clinical Research Nurse Coordinator- Cardiology page is loaded##... ...care and patient monitoring for clinical trials. Responsible... ...the overall clinical study coordination of... ...Research Coordinator will manage clinical research... ...meetings both onsite and off-site as required by study.*...Full timeWork experience placement
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