Senior Clinical Research Associate: Site Monitoring Leader
IQVIA
IQVIA in Overland Park, Kansas, is seeking a Site Manager to perform site monitoring and management work ensuring compliance with study protocols. Responsibilities include conducting monitoring visits, managing site documentation, and supporting recruitment plans. The ideal candidate holds a Bachelor's Degree and has over 3 years of on-site monitoring experience in a clinical setting. Excellent communication and organizational skills are required. The position offers a competitive salary range and benefits. #J-18808-Ljbffr IQVIA
- Join IQVIA, where we value integrity and diversity, and contribute to impactful clinical studies that enhance patient care. #J-18808-Ljbffr IQVIAWebsite
$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$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- 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
$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- ...Senior CRA / CRA II - Home-Based (US) ICON is... ...healthcare intelligence and clinical research organisation united... ...on clinical trial monitoring tasks requiring... ...Monitoring clinical trial sites to ensure adherence to... ...a Clinical Research Associate, with a strong understanding...SeniorWebsiteWork from home
$74.5k - $197.5k
...country where the job is located. Perform monitoring and site management work to ensure that sites... ...contracted scope of work and Good Clinical Practice. Work with sites to adapt, drive... ...in applying, applicable clinical research regulatory requirements such as Good Clinical...SeniorWebsiteFull timePart timeLocal areaImmediate start$101.6k - $169.3k
...based | R1537588 Job Overview Perform monitoring and site management work to ensure that sites are... ...contracted scope of work and Good Clinical Practice. Work with sites to adapt, drive... ...in applying, applicable clinical research regulatory requirements. Good Clinical...SeniorWebsiteFull timePart timeLocal area- ...Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions ICON plc is a world-leading... ...have cardiovascular medical device monitoring experience- however, cardiovascular/... ...mitigate risks and identify issues at sites and implement effective solutions promptly...SeniorWebsiteFlexible 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...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
- ...Abbott is seeking a Senior Safety Coordinator in Kansas City, Missouri to support project teams in implementing safety standards. This role involves monitoring safety conditions, enforcing OSHA policies, and providing safety training. Candidates should have at least 3...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
$87.2k - $169.3k
...Senior CRA 1 IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates... ...seeking a dedicated Clinical Research Associate (CRA) to join our team and play... ...you will be responsible for monitoring and managing clinical sites to ensure compliance with...SeniorWebsiteFull timePart timeImmediate startWorldwide- 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... ...patients. Position Summary The Senior Director, Medical Monitor & Safety Physician is a clinical and safety leader responsible for providing... ...work with colleagues and/or on‑site in San Diego. No role is...SeniorWebsiteTemporary workRemote work- STO Building Group is hiring a Senior Safety Coordinator in Kansas City, Missouri. This role involves upholding environmental, safety, and health standards at construction sites. Responsibilities include monitoring conditions, ensuring compliance with OSHA standards, and...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
- ...leading healthcare organization in Kansas City is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities ensuring... ...strong organizational skills, capable of managing multiple sites efficiently. This role involves high travel, offering a competitive...SeniorWebsite
- ...A growing independent wealth management firm is seeking a Senior Client Relationship Manager in Overland Park, Kansas. The ideal candidate... ..., and ensuring a high-touch client experience. This is an on-site role that allows for long-term growth within the firm, including...SeniorWebsite
- ...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
$78k - $130k
...Positions available: 1 (remote based, Canada) Must be fluent in English and French. Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational...SeniorWebsiteRemote workWork from home$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- Syneos Health/ inVentiv Health Commercial LLC is seeking a Clinical Research Associate to manage clinical trials and ensure compliance with regulatory standards. You will perform site monitoring, manage relationships with site personnel, and maintain project timelines....Website
$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$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
- A leading technology company is seeking a Senior Software Development Engineer in Test (SDET). This role involves designing and maintaining... ...with hands-on experience in AWS and Redis. This position is on-site in Overland Park, KS, promoting high-quality software delivery...SeniorWebsite
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