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
$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...SeniorFull timePart timeWork at officeLocal areaImmediate startWorldwide$74.5k - $197.5k
...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.• i.e., Good Clinical Practice (GCP) and...SeniorFull timePart timeLocal areaImmediate startWorldwide- ...A clinical research organization is seeking a Senior Regional Site Manager in the Kansas City area to oversee clinical trials at investigative sites. The Senior RSM will ensure data quality and integrity while managing relationships with clinical investigators and site...Senior
$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 - United States - Home Based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving... ...as a Clinical Research Associate, with a strong understanding of clinical...SeniorRemote jobWork from homeFlexible hours
- ...ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment... ...Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations...Flexible 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...Local area
- Job Overview Argenta, US Clinical is currently looking for an experienced Clinical Research Associate to join our team. Qualifications 8+ years clinical trial monitor experience within a Clinical Research Organization or a major Animal Health pharmaceutical company....
$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- 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
- 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
$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...- ...accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE * Associate's degree (A.A.) preferred * Two (2) to four (4) years related experience and/or training. * Equivalent combination of...SeniorWork at office
$230k - $295k
...building user experiences that deliver on our customers’ needs by leveraging an innovative infrastructure for money.Collaborating with senior product leadership and other product managers to align roadmaps and conceive projects that support product iterations.Interacting...SeniorFlexible hours- Principal or Senior Principal, Anthropic AI Solutions (Central Region)AI Systems & Platforms | Anthropic Business Unit****Please note: This role is not eligible for 100% remote work. Employees must live within a commutable distance of one the listed offices (Chicago, Il...SeniorTemporary workWork at officeLocal area
- ...material sciences and in the support of clinical studies.In over just 30 years, Eurofins... ...leader who thrives working in cutting-edge research, fosters solid client partnerships, and... ...Viracor BioPharma Services team as a Senior Principal Investigator (SPI)/Principal Investigator...SeniorFull timeContract workWork experience placementWork at officeMonday to Friday
$2,467 per week
...Perks Single Point of Contact First Offer = Best Offer Guaranteed Priority Job Access Comprehensive Benefits Package Clinical Support Extra Ways To Earn Why Clinicians Choose FlexCare Less hassle, more control: one recruiter, transparent pay, and...Full timeContract workImmediate startShift work$2,335 per week
Medical Laboratory Technician Location: Kansas City, KS Agency: Pride Health Pay: $2,335 per week Shift Information: Evenings - 5 days x 8 hours Contract Duration: 13 Weeks Start Date: 8/2/2026 About the Position A Medical Technologist...Full timeContract workShift workAfternoon shift$2,485 per week
Medical Laboratory Technician Location: Kansas City, KS Agency: AHS Staffing Pay: $2,485 per week Shift Information: Days - 5 days x 8 hours Contract Duration: 14 Weeks Start Date: 8/30/2026 About the Position AHS Staffing is looking...Full timeContract workShift work- ...accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE Associate's degree (A.A.) preferred Two (2) to four (4) years related experience and/or training. Equivalent combination of education and...SeniorWork at office
$30 per hour
...update study portals Summary A typical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance... ...all applicable state and local laws. Seniority Level Associate Employment Type Contract Job Function...Contract workWork experience placementLocal area- ...something that adds to our offerings. We learn continuously, both on the job and through formal training programs.Job DescriptionAWD- Senior Business Process AnalystProvide primary process support for CorSo EP to one or more of: Underwriting, Technical Accounting, and...Senior
$96.2k - $151.4k
...primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.... ...Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the study protocol...Full timeFor contractorsLocal areaRemote workRelocationVisa sponsorshipFlexible hoursShift work2 days per week3 days per week- Collins Aerospace is seeking an inspection technician to verify conformance of incoming, in-process, and finished components. You will inspect products from approved suppliers using calibrated devices and an approved sampling plan, raising non-conformances and quarantining...Senior
- ...Research Technician II - Hall Lab Are you fascinated by the bizarre world of small, wiggly, often regenerative invertebrates? The Stowers Institute for Medical Research is seeking a Research Technician II to join the Hall Lab . Our lab is motivated by...Relocation package
- ...A national law firm is seeking a Higher Education Regulatory and Accreditation Senior Counsel in Kansas City. This role requires at least eight years of experience, with a focus on higher education regulatory matters. Responsibilities include advising clients on compliance...Senior
- ...The Bose Lab at University of Kansas Medical Center is seeking a Research Technician to support studies on human bacterial pathogens. Under supervision, you will follow established procedures, maintain records, and generate data for papers and grants. You will manage...
$16.92 - $26.44 per hour
...Scheduled Hours: 37.5 Position Summary Research Technician to work on the production and analysis of antibiotic-like compounds produced by non-pathogenic soil bacteria. Primary Duties & Responsibilities Conduct, evaluate, and maintain experiments. Collect data and perform...Hourly payWork experience placement- ...communities around the world. Organizations infrastructure and culture is amazing. Best place!!Job DescriptionJob Title: Customer Analytics Senior Manager Job Location: Anywhere in USAJob Level: Senior Level Job Description: This is what you will do.. You will help to grow...Senior
- ...Relation Insurance, Inc. in Overland Park, KS is seeking a Senior Manager, Variable Compensation to lead and govern variable pay programs across automated and manual workflows. You will act as the senior escalation point for complex compensation issues and partner with...Senior
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior 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
- senior safety specialist Kansas City, MO
- senior technology project manager Kansas City, MO
- remote senior business analyst Kansas City, MO
- senior manager clinical operations Kansas City, MO
- senior leadership Kansas City, MO


