Clinical Research Associate
ICON
Clinical Research Associate - Oncology - Phoenix 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 accelerate 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 Oncology (Prostate Cancer, and Lung Cancer) and HemeONC clinical trials. 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 50% for on-site monitoring visits across West region; preference given to candidates residing in Phoenix, Arizona 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 #J-18808-Ljbffr ICON
- ...Clinical Research Associate - Oncology - PhoenixICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility,...SuggestedLocal area
- ...Job TitleResponsible 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 and assist in design and...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 subject... ....Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.Good therapeutic and protocol knowledge...SuggestedFull timePart timeLocal areaImmediate startWorldwide$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...SuggestedFull timeFor contractorsLocal areaRemote workFlexible hours2 days per week3 days per week- ...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 participant in the...SuggestedLocal areaRemote workFlexible hoursShift work
- ...Worldwide Clinical Trials is looking for a Senior Clinical Research Associate based in Arizona, working remotely. In this role, you'll manage clinical research activities at various sites, ensuring compliance and conducting study initiation visits (SIVs). Ideal candidates...Remote workWorldwide
- 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
$97k - $193k
Position Overview Clinical Research Associate (CRA) - Worldwide Clinical TrialsAs a CRA, you will work with clinical sites to support research activities across a range of therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases....Work at officeRemote workWorldwide- ..., building strong relationships with investigators and site staff Identify and resolve site-level issues, escalating risks to the Clinical Team Lead/PM as appropriate Review and ensure completeness of essential documents/TMF in line with ICH-GCP and company SOPs Support...Remote work
- Syneos Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to perform vital site qualification and management tasks. You will ensure compliance with regulatory standards and guidelines while safeguarding subject confidentiality....Remote job
- As a Clinical Research Associate (CRA) at Worldwide, you will manage the research activities at sites participating in Worldwide’s clinical research projects. Responsibilities Involved in all stages of the clinical study, including identifying potential sites, performing...Remote jobWork at officeWorldwide
$97k - $193k
...implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts,... ...leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside...Remote jobHourly payWork at officeWorldwide$97k - $193k
Worldwide Clinical Trials, a global CRO, is seeking a Senior Clinical Research Associate (CRA) for remote work in the United States. The role involves managing research activities, conducting study initiation visits, and ensuring compliance with regulatory requirements...Remote jobWorldwide- Responsibilities Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects. Typically involved in all stages... ...5+ years of experience as a Clinical Research Associate 4-year university degree OR Nursing Degree Experience...Remote jobWork at officeWorldwide
$15.15 per hour
A nonprofit organization dedicated to autism research is looking for an Entry-Level Research Associate in Phoenix, AZ. In this role, you will perform data entry... ..., lead participant recruitment, and assist in clinical assessments. The ideal candidate will possess a Bachelor...$100k - $115k
Fortrea is currently seeking Unblinded Clinical Research Associates (CRAs) to join their team in Arizona. The role involves extensive travel and clinical monitoring to ensure high standards in clinical trials. Ideal candidates will have 1-3 years of experience and a degree...Remote job- What You Will Do Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects. Typically involved in all stages... ...5+ years of experience as a Clinical Research Associate. 4‑year university degree or Nursing degree. Experience...Remote jobWork at officeWorldwide
- Syneos Health, Inc. is seeking an Experienced Clinical Research Associate for sponsor-dedicated work. The role supports remote monitoring across sites, ensuring ICH-GCP compliance and data integrity, with substantial travel and collaboration with cross-functional teams....Remote job
- Syneos Health is seeking a Clinical Research Associate for Full-Service supporting remote monitoring across sites in the United States. Responsibilities include site qualification, initiation, interim monitoring, and close-out visits, performed on-site or remotely. The...Remote jobInterim role
- ICON plc is seeking a Clinical Research Associate - Oncology in Phoenix. The role focuses on monitoring sites, ensuring regulatory compliance, and maintaining high-quality data in CTMS/eTMF systems. Travel up to 50% across the West region supports regional coverage. Ideal...
- 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
$97k - $193k
Myana is looking for a Clinical Research Associate to manage research activities in Arizona. The role involves overseeing clinical studies, ensuring compliance, and conducting initiation visits. Ideal candidates will have at least 5 years of experience and strong communication...Remote job$97k - $193k
...implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts,... ...leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside...Remote jobHourly payWork at officeWorldwide$97k - $193k
Position Overview Clinical Research Associate (CRA) at Worldwide Clinical Trials, a global contract research organization (CRO), contributing to clinical research across diverse therapeutic areas. Responsibilities Manage research activities at sites participating in clinical...Remote jobContract workWork at officeWorldwide- Worldwide Clinical Trials is seeking an experienced Clinical Research Associate based in the United States, Arizona. This role involves managing research activities at clinical sites and ensuring compliance with regulations. The ideal candidate will have over 5 years of...Remote jobWorldwide
- ...collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON plc is a world-leading healthcare intelligence and clinical research...Worldwide
- ICON plc is seeking a Clinical Research Associate - Oncology to support Phoenix-area sites. You will act as the main liaison between sites and sponsors, conduct monitoring visits, ensure ICH-GCP compliance, and maintain CTMS/eTMF documentation. This on-site role requires...
- Barrington James is seeking a Senior CRA for a small CRO operating in the US, with responsibility for independent on-site monitoring across sites to ensure regulatory compliance and data quality. You will manage a defined caseload, travel up to 30% for on-site visits, and...
- IQVIA Argentina is seeking a Clinical Research Associate (CRA) in Phoenix, USA. In this role, you'll lead site monitoring visits and ensure high-quality clinical trial execution. Ideal candidates have a Bachelor's degree in life sciences and at least 1 year of monitoring...
- Full‑time Clinical Research, Regulatory Associate Working from our Phoenix, AZ office location, start date August 1, 2026. Why Castle Biosciences? Castle Biosciences Inc. is growing and we are looking to hire a full‑time Clinical Research, Regulatory Associate. Exceptional...Full timeH1bWork at officeVisa sponsorshipWork visaMonday to FridayFlexible hours
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