Senior Clinical Research Associate
$110.52k - $138.15kICON Clinical Research
Senior Clinical Research Associate - Oncology - West 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 elevate 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 3+ years of on-site monitoring experience in the pharmaceutical or CRO industry Experienced monitoring Oncology (i.e. Prostate Cancer and Lung Cancer) and/or Hematology Oncology 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 the West region; preference given to candidates residing in Los Angeles, Phoenix, Seattle, Denver or Portland, 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: $110,520.00-$138,150.00 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. #J-18808-Ljbffr
$110.52k - $138.15k
...ICON in Los Angeles is seeking a Senior Clinical Research Associate specializing in Oncology. You will serve as the primary contact between investigational sites and sponsors, ensuring compliance and supporting patient safety during trials. Qualifications include a Bachelor...Senior- ...As a Senior Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships...SeniorWork visa
$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - West 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...SeniorLocal areaVisa sponsorshipFlexible hours$110.52k - $138.15k
...ICON in Los Angeles is seeking a Sr Clinical Research Associate to conduct clinical trials, ensuring data integrity and patient safety. Ideal candidates will have a Bachelor's degree and a minimum of 5 years' experience in clinical trials. Offering competitive salary between...Senior- ...ICON Clinical Research seeks a Senior Clinical Research Associate in Los Angeles to oversee site compliance and monitoring for Oncology trials. You will be the primary contact between investigational sites and the sponsor, ensuring regulatory adherence. Candidates should...Senior
$65 - $90 per hour
...Overview C-Clinical is looking for an experienced Senior Clinical Research Associate to support clinical trials across the Los Angeles region. This opportunity is well-suited for professionals who enjoy working closely with investigative sites while ensuring high-quality...SeniorHourly payRemote work$145k - $175k
...Piper Companies is currently seeking Senior Contract OncologyClinical Research Associate (SCRA) for an opportunity in Los Angeles California (CA). The Senior Contract Oncology Clinical Research Associate (SCRA) will participate in ongoing Clinical Trials throughout the...SeniorContract workRemote work$80k - $130k
...What This Is What This Is You own IVD diagnostic clinical studies end-to-end — site activation through data lock — across multiple active trials at once. You are not a monitor who writes reports. You are the person who makes studies move. The Culture The Culture RDI runs...Senior$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - West Region ICON 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...SeniorLocal areaVisa sponsorship- ...Senior Clinical Research Associate - Cardio (Smart Pulse 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...SeniorRemote jobFlexible hours
- ...Contract Senior Clinical Research Associate - Home-Based (US) 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...SeniorRemote jobContract workWork from homeFlexible hours
- ...Senior CRA / CRA II - Home-Based (US) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation... ...experience as a Clinical Research Associate, with a strong understanding of...SeniorRemote jobWork from homeFlexible hours
- ...Job Title Responsible for providing Clinical Research support for all clinical trials. Job Information Date Opened 04/02/2026 Job Type: Full time Industry: Pharma Work Experience: 0-1 year Salary: 85000 City: Los Angeles State/Province: California...Full timeWork experience placement
$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)...Full timePart timeLocal areaImmediate startWorldwide$30.16 - $34.4 per hour
...The University of Southern California is seeking an Instructional Lab Technician (Senior) in the Dornsife Academic Support Hub. This role focuses on coordinating lab exercises, conducting experiments, and ensuring compliance with safety standards. Preferred qualifications...SeniorHourly pay- ...Cedars-Sinai Medical Center is seeking a Clinical Research Associate I in Los Angeles, CA. This role involves coordinating clinical studies, evaluating research data, ensuring compliance with regulations, and managing patient contact under supervision. Candidates should...
- ...considered. Cedars‑Sinai has an outstanding opportunity for an independent and well‑organized contributor to serve as a CLINICAL RESEARCH ASSOCIATE II to Dr. Judy Tan to support community‑engaged research that develops behavioral and community‑based health interventions...Local areaRemote work
- ...Cedars-Sinai Medical Center in Los Angeles is looking for a Clinical Research Associate I to manage and implement clinical research studies. You will evaluate research data, assist with regulatory submissions, and coordinate patient visits. An ideal candidate has a Bachelor...Local area
- ...execution of treatment-use and clinical support activities by... ...team. Supports activities associated with out-of-specification programs... ...works with multiple contract research organizations and external partners... ...issues appropriately to senior management. Prepares metrics...Contract workInterim role
- ...The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives...Local area
- ...our team, you?ll have access to groundbreaking biomedical research facilities and world-class medical education programs. We... ...patient outcomes. What will you be doing in this role? The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research...Local area
$20 - $27 per hour
...Parexel International is hiring a Research Associate in Glendale, CA to support Phase I clinical trials. This role requires customer service and clinical research experience. Responsibilities include recruiting participants, conducting screenings, and maintaining study...Hourly pay- ...Direct Jobs is hiring a Clinical Research Associate II in Los Angeles, California. This role requires onsite collaboration and supports community-focused health interventions for LGBTQ+ communities. The candidate will work closely with diverse research teams and manage...
- ...Itlearn360 is looking for a Clinical Research Associate I in Los Angeles, CA, to assist in coordinating and implementing clinical studies. The role involves evaluating research data, ensuring protocol compliance, and completing case report forms. Candidates should have...
$20 - $27 per hour
...Parexel International is seeking a Research Associate in Glendale, Arizona. In this role, you will support early phase clinical trials by recruiting participants, conducting necessary medical procedures, and maintaining study documentation. The ideal candidate has clinical...Hourly pay- ...The Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. Supports...Daily paidLocal area
- ...Itlearn360 is seeking a Clinical Research Associate II to oversee the execution of non-therapeutic clinical research studies at the Ellison Institute in Los Angeles, CA. The role involves ensuring compliance with study protocols, quality control of data, and collaboration...
- ...Cedars-Sinai Medical Center in Los Angeles is seeking a Clinical Research Associate I to join our team. The successful candidate will coordinate clinical research efforts, maintain compliance with regulatory guidelines, and assist with patient contact as necessary. A High...
- ...Women Veterans Interactive is looking for a Clinical Research Associate I in Los Angeles, California. The role involves assisting in the coordination and implementation of research studies, including data collection and compliance with federal guidelines. Candidates should...
- ...Clinical Research Associate I When the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. We invite...Daily paidLocal areaImmediate startShift work
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