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
$100k
...subject protection is maintained, Good Clinical Practice (GCP), and applicable regulations... .... • Understanding of clinical research processes and regulations. • Certifications... ...Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical...SuggestedFull timeContract workInterim roleLocal 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...SuggestedPermanent employmentWork at officeRemote work$71.9k - $189k
...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 therapeutic and protocol...SuggestedFull timePart timeLocal areaImmediate startWorldwide$100k - $110k
...Piper Companies is seeking a Clinical Research Associate II to join a global organization within the clinical research and life sciences industry for a remote permanent role with 60-75% travel across the United States. This CRA II will support cardiovascular, CNS, and...SuggestedPermanent employmentRemote work- ...Overview Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for a leading organization within the life sciences and pharmaceutical research industry. The Clinical Research Associate (CRA) role is ideal for an experienced...SuggestedRemote work
$60k - $80k
...searching for talented and passionate people who want to help shape the future of veterinary care. About the position The Vet Clinic Implementation Associate at Vetcove is responsible for overseeing the end‑to‑end management of large‑scale projects that enhance the customer...Hourly payFull timeRemote workHome office- ...NYU Grossman School of Medicine invites applications for a Research Associate (Per Diem) in CSTAR. You will support clinical and translational studies, recruit participants, collect data, and handle specimens while maintaining documentation and coordinating with study...Daily paidDay shiftAfternoon shiftEarly shift
- ...organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to... .../patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies...Contract workInterim roleLocal areaImmediate startRemote workWork from homeFlexible hours
- ...Montefiore Orthopedics is seeking a Research Associate I to oversee multiple clinical trials. You will serve as the main point of contact for patients, families, and study teams, coordinating across hospital departments to ensure timely completion of trial activities....
- ...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...
$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- ...Montefiore Hudson Valley Collaborative seeks a Research Associate I to manage multiple clinical trials as a patient-facing liaison and trial team lead. You will work with departments hospital-wide to ensure timely completion of trial-related activities, maintaining protocol...
- Syneos Health is seeking a CRA II for sponsor-dedicated oncology/neurology work (home-based in GA/SC). The role involves site qualification, monitoring, data review, and regulatory compliance across real-world late-phase studies. Travel up to 30% is required, with on-site...Remote workWork from home
- ...NAMSA, a leader in medical device materials testing, seeks a Clinical Research Associate to ensure human subject protection, GCP compliance, and regulatory adherence across studies. You will coordinate site monitoring, conduct qualification visits, and support study start...
- ...Montefiore New Rochelle seeks a Research Associate I to oversee multiple clinical trials, acting as a primary contact for patients and study teams. The role involves coordinating with multiple departments to ensure timely completion of trial activities and adherence to...
- ...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...
- Title: Clinical Research Associate *This role is located in either New York or New Jersey The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA...Hourly payTemporary workLocal areaRemote work
$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- Parexel International is seeking an FSP CRA with 3+ years of CRA experience from Australia or New Zealand. The position is based in NSW or VIC and focuses on overseeing site monitoring and study conduct. You will manage site activation through database lock, coach site...
$4,000 - $9,000 per month
...Clinical Research Associate DotLab is transforming the diagnosis and management of endometriosis, a disease that affects 1 in 10 women worldwide and currently requires surgery to diagnose. The disease is the cause of over half of unexplained infertility, and is a primary...Work experience placementWork at officeRemote workWorldwideFlexible hours- ...Freenome is seeking a Contract Clinical Research Associate to join its Clinical Development team, working remotely with occasional travel to California. The ideal candidate will manage all aspects of clinical trial monitoring and is expected to deliver excellence in compliance...Contract workRemote work
- ...A medical device company focused on cervical spine conditions is seeking a Clinical Research Associate. Responsibilities include managing clinical trials, ensuring compliance, and coordinating operations with study sites. The ideal candidate will have 3-5 years of clinical...Remote work
$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 and regulations, protocol, site monitoring plan and associated documents. Gain an in-depth understanding of the study protocol...For contractorsLocal areaRemote workRelocationVisa sponsorshipFlexible hours2 days per week3 days per week- ...A healthcare organization is seeking a Research Associate to work with Principal Investigators in clinical research studies. Responsibilities include overseeing data integrity, managing study information, and preparation of research presentations. Candidates should have...
- ...EPM Scientific is currently partnering with a leading Cardiovascular Medical Device company that is seeking an experienced Clinical Research Associate Contractor on a remote basis. Key Requirements Proven experience as a CRA within the cardiovascular medical device field....Contract workFor contractorsFreelanceImmediate startRemote work
$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- ...human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement... ...opportunity to join our team as a Senior Clinical Research Associate to support our Clinical Operations team. The Sr. CRA will participate...Work experience placementWork at officeRemote workShift work
- 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...Full time
- TheSenior Clinical Research Associateis responsible for the overall operational execution of clinical studies on one or more clinical projects... ..., shipment, and storage as, well as maintenance of associated tracking information Train CROs, vendors, investigators, and...
$103k - $130k
Sr. Clinical Research Associate (Sr. CRA) The Sr. Clinical Research Associate (Sr. CRA) is responsible for the set‑up, initiation, execution, monitoring and close‑out of IVD and medical device clinical trials at external clinical research sites and/or laboratories. The...Contract workRemote workNight shift
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