Clinical Research Associate
ICON
Clinical Research Associate - St Louis/Kansas City/Ohio ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports. Your profile Bachelor's degree in a scientific or healthcare-related field. Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license. What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being. Life assurance Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. #J-18808-Ljbffr ICON
$71.9k - $182k
...Clinical Research Associate (CRA) 2 Level IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic, Oncology, and/or Neurology. Candidates...SuggestedFull timePart timeLocal areaImmediate startWorldwide- Clinical Research Associate - Multi TA ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the...SuggestedFlexible hours
- ...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...SuggestedLocal area
- ...Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you...SuggestedFlexible 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 adhere to all protocols, regulations, and sponsor requirements. Essential Functions Site Monitoring: Conduct selection...SuggestedFull 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-1), diabetes, GI, MASH/NASH, dermatology, or respiratory: Job Overview Perform monitoring and site management work to ensure that...Full timePart timeLocal areaImmediate start$87.2k - $169.3k
...Senior CRA 1 IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase 1 experience across... ..., US. Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful...Full timePart timeImmediate startWorldwide- 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...Remote work
- Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
$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 scientific...Work at office$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...Remote workWork from home- ...collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON plc is a world-leading healthcare intelligence and clinical research...Worldwide
$71.9k - $189k
Senior Clinical Research Associate, Sponsor Aligned, Oncology Overland Park, United States of America | Full time | Field-based | R1541483 Job Overview Join our dynamic team as a Clinical Research Associate! You’ll play a pivotal role in monitoring and managing clinical...Full timePart timeWork at officeLocal areaImmediate startWorldwide- Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to manage site activities focusing on regulatory and protocol compliance. The role requires a Bachelor's degree in a related field and strong communication skills, with responsibilities...Remote job
- Clinical Research Associate - Full-Service Syneos Health is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success and improving patient outcomes. Job Responsibilities Perform site qualification, site initiation, interim monitoring...Interim roleLocal areaImmediate startRemote workFlexible hours
$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...Work at officeLocal area$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...$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 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...
- 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...
$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...$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...- .... As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol... ...standards. We are currently seeking a Lead Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Lead CRA at...Worldwide
- Join IQVIA, where we value integrity and diversity, and contribute to impactful clinical studies that enhance patient care. #J-18808-Ljbffr IQVIA
$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- 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...
$30 per hour
...reminders, update study portals Summary A typical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance of... ...state and local laws. Seniority Level Associate Employment Type Contract Job Functionರುವ>...Contract workWork experience placementLocal area- The University of Kansas Medical Center is seeking a Clinical Research Assistant (Temporary) in Cardiology to support clinical research activities within the Department of Cardiovascular Medicine. This role requires conducting informed consent discussions, coordinating...Temporary work
$22.88 - $33.17 per hour
The University of Kansas Medical Center in Kansas City seeks a Clinical Research Assistant for the Division of Physical Activity and Weight Management. This role involves delivering health education and exercise instruction, working with diverse populations, including those...Hourly pay$22.88 - $33.17 per hour
The University of Kansas Medical Center is seeking a Clinical Research Assistant - Internal Medicine for the Weight Management department. This role involves assisting in the implementation of physical activity and nutrition interventions for various populations. Responsibilities...Hourly payFull time
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Associate. Be the first to apply!
- on-site clinical research associate (traveling/remote) Kansas City, MO
- clinical research administrator Kansas City, MO
- clinical trials assistant Kansas City, MO
- clinical research assistant Kansas City, MO
- clinical research associate Kansas City, MO
- clinical research remote Kansas City, MO
- clinical research manager remote Kansas City, MO
- clinical trial lead Kansas City, MO
- clinical research part time Kansas City, MO
- clinical research monitor Kansas City, MO

