Sr. Clinical Research Associate
ICON Clinical Research
Sr. Clinical Research Associate 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. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. Responsibilities You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross‑functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Qualifications You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Bachelor's degree in a relevant scientific discipline or healthcare-related field. Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem‑solving skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. Willingness to travel as required (approximately 60%). Benefits 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. 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 Clinical Research
$120k - $140k
...Remote Sr. CRA position in the oncology space! This Jobot Job is hosted by: Audrey Block Are you a fit? Easy Apply now by clicking... ...and escalates per protocol to upper management Work with in-house Clinical Trial Assistant to collect, review, and monitor required...SeniorInterim roleLocal areaRemote workFlexible hours- ## Senior Clinical Research Associate - Psychiatry - East Coast - RemoteApplyremote type: Remotelocations: Research Triangle Park, North Carolinatime type: Full timeposted on: Posted Yesterdayjob requisition id: JR102111**Who we are**We’re a global, midsize CRO that pushes...SeniorWork at officeRemote workWorldwide
- ...Parexel FSP is looking for a CRA/Sr CRA in the US. Oncology Experience required. Cell therapy experience is strongly preferred. Job Purpose: The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is...SeniorLocal areaRemote workFlexible hoursShift work
- A clinical research organization in Raleigh, NC, seeks a Senior Clinical Research Associate to manage site activities for multiple protocols. The role requires a Bachelor’s or Master’s degree in health-related fields and offers substantial career support. You'll conduct...SeniorRemote job
- Position: Senior Clinical Research Associate (level dependent on experience) Location: Raleigh, NC Job Id: CRA Ongoing NC # of Openings: 1 Job Purpose/Summary To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing...SeniorLocal areaRemote workWork from homeHome office
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- Grifols is seeking a Clinical Research Associate to manage clinical monitoring processes and ensure regulatory compliance. You will track study tasks, conduct monitoring visits, and facilitate investigator site interactions to support clinical trials. The ideal candidate...Senior
- ...implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright... ...Clinical Operations Department does at Worldwide**Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research...SeniorRemote jobWork at officeWorldwide
- Syneos Health/ inVentiv Health Commercial LLC is hiring an Experienced Clinical Research Associate in North Carolina. This role involves site management, regulatory compliance, and ensuring that clinical trials operate smoothly. Candidates should have a Bachelor's degree...SeniorRemote jobFlexible hours
- ...The Clinical Research Associate (CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical...Local areaRemote work
- RHO in North Carolina is seeking an In-House Clinical Research Associate who will gain vital experience towards becoming a traveling CRA. Responsibilities include managing data, assisting on query resolutions, and ensuring compliance with regulatory standards. This role...
- The Clinical Research Associate assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols. Ensures coordination of an accelerated study start-up including...Interim role
$55k - $65k
...creating a safe environment to innovate and develop over a long and rewarding career. We are currently hiring an In‑House Clinical Research Associate to join our team! As an In‑House CRA here at Rho, you’ll have the opportunity to gain the necessary experience to grow...Hourly payWork experience placementCurrently hiringLocal areaRemote work- Clinical Research Associate II - Oncology (North Carolina/South Carolina) AbbVie’s mission is to discover and deliver innovative medicines. The Clinical Research Associate II (CRA II) advances AbbVie’s pipeline through superior clinical research, partner with investigators...Contract workTemporary workLocal area
- Columbus, United States | Posted on 07/16/2025 Industry Pharma/Biotech/Clinical Research Work Experience 1-3 years City Columbus State/Province Arkansas Country United States Job Description Responsible for providing Clinical Research support for all clinical trials. Under...Work experience placement
- Overview Experienced Clinical Research Associate - Full-Service 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...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
$115k - $125k
Senior Clinical Research Associate Piper Companies is currently seeking aSenior Clinical Research Associate (CRA) for an opportunity in North Carolina. The Senior Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a...SeniorRemote work- A leading biopharmaceutical solutions organization is seeking an Experienced Clinical Research Associate to oversee site monitoring, ensuring compliance with regulatory requirements and clinical protocols. Responsibilities include conducting site visits, managing site activities...SeniorRemote jobWorldwide
$70.1k - $126.1k
...candidates will hold a Bachelor’s degree or equivalent in a related field, possess strong communication skills, and have knowledge of Good Clinical Practice guidelines. The position offers a competitive salary range of $70,100.00 - $126,100.00 along with various benefits...SeniorRemote jobWork from homeFlexible hours- Grifols, S.A is seeking a Clinical Research Associate in North Carolina to ensure site adherence to regulatory requirements and GCP Guidelines. You will manage site start-up and monitor clinical trials while maintaining project timelines and compliance. The ideal candidate...
- A leading clinical research company in North Carolina is seeking a Clinical Research Associate to provide support for all clinical trials. The role involves preparing protocols, monitoring studies, and ensuring compliance with guidelines. Ideal candidates should have a...
- A clinical research organization in Raleigh is seeking a Clinical Research support professional. The role involves assisting in the design and preparation of studies, conducting monitoring visits, and preparing reports for clinical trials. Candidates should possess a BA...
- ...Description Experienced Clinical Research Associate - Full-Service- West Coast Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- Experienced Clinical Research Associate - Full-Service- West Coast Updated: April 16, 2026 Location: Morrisville, NC, United States Job ID: 25107805 Description Experienced Clinical Research Associate responsible for site qualification, initiation, monitoring, management...Interim roleLocal areaRemote work
- A public research university in North Carolina seeks a Soc/Clin Research Assistant to support faculty with various research projects. Responsibilities... ..., entry, and monitoring, ensuring compliance with FDA and Good Clinical Practice. Candidates must hold a Bachelor's degree and display...Full timeTemporary work
- A leading clinical research organization is seeking an experienced Clinical Research Associate in Morrisville, NC. The role involves site qualification, monitoring, and ensuring compliance with regulatory guidelines. The ideal candidate holds a Bachelor's degree or RN...Remote job
- Position Summary The position will involve assisting with clinical neuromodulation research focused on analyzing deep brain stimulation (DBS) lead... ...lead placement, target brain region response, and factors associated with differences in therapeutic efficacy and recovery...
- The University of North Carolina at Chapel Hill is seeking an individual to assist with clinical neuromodulation research, particularly analyzing deep brain stimulation efficacy in movement disorder patients. Responsibilities include managing patient research databases...
$163.9k - $235.55k
Why UKG: At UKG, the work you do matters. The code you ship, the decisions you make, and the care you show a customer all add up to real impact. Today, tens of millions of workers start and end their days with our workforce operating platform. Helping people get paid...SeniorLocal areaShift work$143k - $243k
A leading pharmacy benefit management firm is seeking a Senior Principal Actuary to provide actuarial direction and innovative modeling. The role involves collaborating with underwriters, leading actuarial staff, and monitoring health policy impacts. Candidates should ...SeniorRemote work
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