Sr. Clinical Research Associate
ICON Strategic Solutions
Sr. Clinical Research Associate - South East 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. What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: 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. Your Profile: You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience: 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%) 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
$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- ...management activities to ensure compliance with regulatory standards. The successful candidate will leverage their knowledge of Good Clinical Practice and manage site-related activities while supporting patient recruitment. Join a passionate team dedicated to making a...Senior
- ...Parexel International is seeking a Clinical Research Associate (CRA) to manage and monitor investigator sites for clinical trials in the United States. This role involves ensuring patient safety, compliance with regulations, and effective site management. The ideal candidate...Senior
- ...A biotechnology company is looking for a Senior Clinical Research Associate to oversee clinical trials in the United States. The position requires extensive experience in clinical research, particularly in oncology, with responsibilities including site management, regulatory...SeniorRemote work
$105k - $117k
...A leading clinical outsourcing company seeks an Experienced Ophthalmology & Gen Med CRA 2 to join their Full Service Outsourcing team. This role involves extensive site monitoring, collaboration with study teams, and ensuring patient protocol compliance. Candidates should...SeniorRemote work- ...We are working with a fast growing organization who is seeking to bring on experienced Clinical Research Associates located nationwide. The role requires limited to no travel and offers a tremendous opportunity to partner with a growing, high-quality and innovative team...SeniorInterim role
- ...Our Client is a rapidly growing international Clinical Research Organisation offering an experienced( Senior ) CRA opportunity to work from home on full FTE as part of their team in Spain . Responsibilities: Conducting start-up activities and monitoring visits Maintaining...SeniorWork from home
- ...Kelly Science and Clinical FSP is currently seeking a Regional Clinical Research Associate for a long-term engagement in the US with one of our Global Medical Device clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution...SeniorFull time
- ...Senior Clinical Research Associate (US) Remote Position Summary The Sr. CRA is responsible for the oversight and monitoring clinical trials to ensure they are conducted in compliance with the study protocol, ICH-GCP guidelines, applicable regulations, and company SOPs....SeniorInterim roleRemote work
- ...ABBVIE is seeking a Clinical Research Associate to oversee clinical trials in the NJ/PA area. The role requires engaging with investigative sites, training staff, and ensuring compliance with study protocols. Qualified candidates will have a tertiary qualification in health...Senior
- ...Senior Clinical Research Associate - Cardio (Smartpulse 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...SeniorFlexible hours
- ...Senior Clinical Research Associate job at PSI CRO. Remote. We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated...SeniorRemote workWork from homeWork visa
- ...requirements Prepare, organize and submit IRB documentation for clinical trials Process and submit IND safety reports as delegated by... ...clinical trial operations What you’ll bring 2–6 years of clinical research experience, including at least 2 years in regulatory affairs or...SeniorLocal areaWork from homeFlexible 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...SeniorLocal areaRemote work
- ...A leading clinical research organization is seeking a CRA II to manage study sites and ensure compliance with protocols. Responsibilities include overseeing patient safety, conducting site visits, and preparing monitoring reports. The ideal candidate will have a minimum...SeniorNight shift
- ...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 an active...SeniorLocal areaRemote workFlexible hoursShift work
$91.34k - $114.17k
...coast ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment... ...Advert Posting We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research...SeniorWork experience placementFlexible hours- ...Philips International in Plymouth is seeking a Senior Clinical Research Associate to oversee clinical studies, ensuring adherence to protocols, regulatory standards, and data integrity. The ideal candidate will have over 5 years of experience in Clinical Research within...Senior
$38 - $40 per hour
...exclusive features. Direct message the job poster from Baim Institute for Clinical Research Director, Human Resources at Baim Institute for Clinical Research The Sr. Clinical Research Associate/Field Monitor Contractor performs remote and on-site visits, such as, Qualification...SeniorPart timeFor contractorsInterim roleRemote workWork from home10 hours per week$125k - $145k
...Senior Clinical Research Associate (Pain/Oncology/CNS Therapeutic Areas) Key Accountabilities Interact with personnel from study Sponsors, investigational sites, vendors, and Everest functional groups to enable quality and on-time execution of clinical trials in compliance...SeniorContract workTemporary workInterim roleLocal areaRemote work- ...Syneos Health is looking for a Clinical Research Associate II (CRA II) in the United States. This role involves performing site qualification, site initiation, monitoring activities, and ensuring regulatory compliance. The ideal candidate will have a Bachelor's degree...Senior
- ...ProTrials Research, Inc. is seeking a Contract Senior Clinical Research Associate to oversee clinical trial monitoring and management. This role involves ensuring compliance with protocols and SOPs while managing site personnel training and documentation. The ideal candidate...SeniorContract work
$102k - $162k
...Job TitleSenior Clinical Research AssociateJob DescriptionThe Senior Clinical Research Associate is responsible for developing comprehensive study plans/protocols, ensuring adherence to ISO/FDA regulatory requirements, Good Clinical Practice (GCP) guidelines, and study...SeniorFull timeWork at officeImmediate startRemote workWork visa3 days per week$108.7k - $139.8k
...All Jobs Senior Clinical Research Associate The Senior Clinical Research Associate is a senior individual contributor and leader within the EBR Clinical organization, accountable for monitoring excellence, data integrity, and site engagement across the full lifecycle...SeniorContract workWork at officeRemote workNight shift- ...Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to perform site management and ensure compliance with regulatory standards. Responsibilities include site qualification, monitoring, and documentation as well as acting...SeniorRemote workFlexible hours
- ...ICON Strategic Solutions is looking for a Clinical Research Associate who will lead clinical trial monitoring with a focus on quality and continuous improvement. The individual will ensure adherence to protocols and conduct site visits to support successful trial execution...Senior
- ...Parexel International is seeking a Senior Clinical Research Associate in Idaho to manage and monitor clinical trial sites. This role ensures compliance with regulatory standards and oversees investigator relationships to promote patient safety and study quality. A Bachelor...Senior
- Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to perform site management and ensure compliance with regulatory standards. Responsibilities include site qualification, monitoring, and documentation as well as acting as...SeniorRemote jobFlexible hours
$65 - $90 per hour
...Job Description We are looking for an experienced Senior Clinical Research Associate with a strong background in medical device studies and independent... ...Compensation: $65 - $90 hourly Responsibilities: ~ Sr. CRA (Remote / Home-Based with on-site travel required) ~...SeniorHourly payContract workLocal areaRemote workWork from home- A healthcare organization based in New York seeks a Senior Research Associate to lead clinical trial activities. The role involves mentoring junior associates, ensuring timely data collection, and contributing to research protocol development. Ideal candidates will possess...Senior
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