Senior Clinical Research Associate
ICON
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 to join us on our mission to shape the future of clinical development. To support 1 study in the cardiovascular/electrophysiology medical device space. Indication is A-fib. The ideal candidate will have cardiovascular medical device monitoring experience- however, cardiovascular/electrophysiology pharma monitoring experience will be considered. 3 years of monitoring experience required. A bachelor’s degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science. Candidates must have/ be: In-depth knowledge of FDA regulations and ICH/GCP guidelines. Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly. Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams. Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely. Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment. Ability to work independently and manage multiple priorities in a dynamic environment. A well‑executed plan for communication with the study teams and sites. Well‑versed in clinical trial management. They are rigorous, detail‑oriented, and precise in their reports. Located in the US near a major airport. Ability to cover up to 65% regional travel. 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. 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. 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. Visit our careers site to read more about the benefits ICON offers. 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. 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 here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply. #J-18808-Ljbffr ICON
- 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
- ...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...SeniorFlexible hours
$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 of therapeutics. Seeking... ...Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in...SeniorFull timePart timeImmediate 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...SeniorRemote job
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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...SeniorWork at officeLocal area- ...Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All Regions ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation...Senior
- ...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...SeniorWorldwide
- 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 - $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...SeniorFull timePart timeWork at officeLocal areaImmediate startWorldwide$71.9k - $189k
...Clinical Research Associate 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...SeniorFull timePart timeWork at officeLocal areaImmediate startWorldwide- 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...Senior
$101.6k - $169.3k
...out visits) in accordance with contracted scope of work and Good Clinical Practice. Work with sites to adapt, drive, and track subject... ...Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. Good Clinical Practice (GCP) and International...SeniorFull timePart timeLocal area$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...SeniorFull timePart timeLocal areaImmediate startWorldwide$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...SeniorRemote workWork from home- ...Senior CRA / CRA II - Home-Based (US) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation... ...experience as a Clinical Research Associate, with a strong understanding of...SeniorRemote jobWork from homeFlexible 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...Full timePart timeLocal areaImmediate startWorldwide$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 ...Work at office$71.9k - $145.3k
...Study Start-Up Clinical Research Associate, Sponsor Dedicated page is loaded## Study Start-Up Clinical Research Associate, Sponsor Dedicatedlocations: Overland Park, KS, United States of America: Carlsbad, CA, United States of America: Durham, North Carolina, United States...Full 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...Flexible hours
$66.8k - $120k
...Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and...Temporary workWork at officeRemote workHome officeNight shift$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...- 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
- 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 - $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...- Join IQVIA, where we value integrity and diversity, and contribute to impactful clinical studies that enhance patient care. #J-18808-Ljbffr IQVIA
- 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...$71.9k - $119.9k
IQVIA Argentina is looking for a Clinical Research Associate I (CRA I) based in Kansas City, Missouri. This role supports clinical research studies by performing site monitoring and ensuring compliance with protocols and regulations. The ideal candidate will have a degree...- ...treatments that benefit patients worldwide. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted... .... We are currently seeking a Lead Clinical Research Associate (CRA) to join our diverse and dynamic team. As...Worldwide
$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'...
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