Clinical Research Associate
$91.34k - $114.17kICON Clinical Research
Clinical Research Associate - Multi Therapeutic Area (Early Development) - West Region 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. What You Will Be Doing: Serve as the primary point of contact between investigational sites and the sponsor Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out Ensure site compliance with ICH-GCP, SOPs, and regulations Maintain up-to-date documentation in CTMS and eTMF systems Support and track site staff training and maintain compliance records Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting Support subject recruitment and retention efforts at the site level Oversee drug accountability and ensure proper storage, return, or destruction Resolve data queries and drive timely, high-quality data entry Document site progress and escalate risks or issues to the clinical team Assist in tracking site budgets and ensuring timely site payments (as applicable) Collaborate with cross-functional partners including CTAs, LTMs, and CTMs You are: A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN Eligible to work in United States without visa sponsorship A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry Experienced monitoring early development Phase I/II clinical studies, across multiple therapeutic areas Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF A clear communicator, problem-solver, and collaborative team player Willing and able to travel up to 60% for on-site monitoring visits across the West region; preference given to candidates residing in West region near major HUB airports to support efficient 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. Salary range: $91,336.00-$114,170.00 Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Are you a current ICON Employee? Please click here ( to apply ICON Clinical Research
- ...Job Description Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate...Suggested
$71.9k - $189k
...out visits) in accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt, drive, and track... ...Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. • i.e., Good Clinical Practice (GCP)...SuggestedFull timePart timeLocal areaImmediate startWorldwide- ...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...SuggestedFull time
- ...institutions and leading players in biopharma and translational research. We’re bringing the best minds together to accelerate... ...proven playbook to make it happen, from hospital labs to mobile clinics. By helping providers, patients, and families get faster, more...SuggestedWorldwide
$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - New York 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...SuggestedWork experience placementInterim roleLocal areaRemote workFlexible hours$110.52k - $138.15k
...Senior Clinical Research Associate - Northeast 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...Work experience placementFlexible hours$103k - $130k
...players in biopharma and translational research. We're bringing the best minds together... ...it happen, from hospital labs to mobile clinics. By helping providers, patients, and families... ...possible. The Sr. Clinical Research Associate (Sr. CRA) is responsible for?set-up,...Hourly payContract workRemote workWork from homeWorldwideFlexible hoursNight shift- ...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...Interim role
- ...mostly on-site data monitoring is a flag; covering all visit types evenly is needed. Experience in creating (not just reviewing) clinical documents such as training materials for SIVs, protocols, CRFs, ICFs, and brochures. Experience participating in Data Management activities...Remote workFlexible hours
$120k - $135k
...in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most... ...patients globally.Role Overview:We are seeking a Senior Clinical Research Associate (CRA) to support our Clinical Operations team. The Senior...Temporary workWork at officeImmediate startVisa sponsorship$71.9k - $169.3k
...trusted partnerships that help bring breakthrough treatments to patients faster. Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you...Full timePart timeImmediate startWorldwide$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...Contract workWork at officeRemote workNight shift$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...Full timeWork at officeImmediate startRemote workWork visa3 days per week$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...Part timeFor contractorsInterim roleRemote workWork from home10 hours per week$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 area$58.66k - $81.68k
...Job Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre-clinical, Phase I through Phase IV, and post-marketing studies...TraineeshipLocal area$120k - $140k
...and resolves site performance, quality, or compliance problems and escalates per protocol to upper management Work with in-house Clinical Trial Assistant to collect, review, and monitor required regulatory documentation for study start-up, study maintenance, and study...Interim roleLocal areaRemote workFlexible hours- A leading clinical research organization in New York is seeking a Cancer Clinical Trials CRC I to support clinical trial operations under supervision. Responsibilities include data collection, patient recruitment, and managing informed consent processes. Applicants should...
- 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 I/II Benefits include: Medical, Dental, and Vision Insurance, 401(k), Stock Options NOTE: You must have a minimum of 3-5 years prior experience combined in-house and field monitoring to be considered for this position (medical device experience...Local areaRemote workWorldwide
- Overview As a clinical research associate (CRA), you are responsible for completing clinical research and administrative tasks for clients. You facilitate documentation for clinical research. As a CRA, you monitor clinical tasks for correct functioning and completion, evaluate...RelocationVisa sponsorship
- A leading healthcare organization in New York is seeking a Research Associate to oversee clinical trials. The role requires strong clinical research skills, a Bachelor's degree, and GCP training. Responsibilities include managing daily trial activities, ensuring compliance...
- ...autoimmune disease, with unmet medical needs worldwide. InnoCare has built up a fully integrated platform in terms of research and development, clinical development, manufacturing and commercialization. To date, the Company has developed a robust product pipeline...Worldwide
$53.36k - $67.81k
...Clinical Research Associate I - Clinical Trial Charge Monitoring We are seeking a detail-oriented and analytical team member to ensure accurate, compliant, and timely billing of clinical trial related services. This role supports the integrity of our research billing...Work at office- A clinical research organization is seeking Clinical Research support in Pennsylvania. The role involves assisting with clinical trials, including protocol design, regulatory document management, and site evaluations. Candidates should have a BA or equivalent, basic knowledge...
- Objective As a Clinical Research Associate II (CRA II) specializing in oncology, you will play a crucial role in the execution and management of Phase 1, Phase 2, and Phase 3 clinical trials. You will collaborate closely with cross‑functional teams to ensure adherence to...Interim roleLive inLocal areaRemote work
$115k - $125k
Piper Companies is seeking a Clinical Research Associate (CRA) to join a global leader in clinical research and healthcare analysis for a remote permanent position located based out of CST . The Clinical Research Associate (CRA) will travel to sites 8-10 days out of the...Permanent employmentWork at officeRemote work- A clinical research organization is seeking a Clinical Research support professional in New York, NY. The role involves assisting in the design of protocols, managing regulatory documents, and conducting ongoing study monitoring. Candidates should possess a degree in a...
- Mount Sinai Morningside in New York is seeking a Clinical Research Associate I to monitor clinical trials from site management through maintenance and closure across Phase I-IV and post‑marketing studies. You will prepare and edit key study documents, maintain the clinical...
- ...language model-based system built to understand and assess clinical characteristics in EMRs. Synapsis AI is designed for installation... .... As a vital member of our diverse team, our Clinical Research Associates (CRA) will collaborate closely with the AI Research and software...Local areaFlexible hoursShift work
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