Clinical Research Associate
ICON
Clinical Research Assoicate 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 CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced 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 #J-18808-Ljbffr
- ICON plc is a world-leading healthcare intelligence and clinical research organization. We are seeking a CRA II to design and analyze clinical trials, interpret data, and contribute to innovative treatments and therapies. You will conduct site visits, ensure protocol compliance...Suggested
$91.34k - $114.17k
Clinical Research Associate - Oncology - West RegionICON 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...SuggestedFull timeLocal area$110.52k - $138.15k
Senior Clinical Research Associate - Oncology - Southern CaliforniaICON 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...SuggestedFull timeInterim roleLocal areaRemote work$110.52k - $138.15k
Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All RegionsICON 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...SuggestedFull time$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$33.65 - $48.08 per hour
CRA Administration Officer (NE) (Project Management) People Drive Our Success Are you enthusiastic, highly motivated, and have a strong work ethic? If yes, come join our team! At Cathay Bank – we strive to provide a caring culture that supports your aspirations and success...Full timeWork at officeFlexible hours- ...Clinical Research Associate To be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study...Local area
- ...Cedars-Sinai's Smidt Heart Institute in Los Angeles invites applications for a Clinical Research Associate I/CPT. You will assist in coordinating noncomplex research studies under supervision, supporting data collection, regulatory submissions, budgeting, and study logistics...
- Cathay Bank in El Monte, CA seeks a CRA Investments Officer (Project Management) to support CRA investments and Foundation grants. You will analyze documentation, track CRA activity, and assist with the CRA Compliance Program. The role requires a Bachelor's degree in Business...
- ...Cedars-Sinai is hiring a Clinical Research Associate I to work in the Smidt Heart Institute. This role involves coordinating studies with a Clinical Research Coordinator and ensuring compliance with research protocols. Ideal candidates will have a high school diploma and...
- Cathay Bank in California seeks an AVP, Community Outreach Officer (Project Management) to lead CRA outreach efforts with nonprofits and CDFIs, plan and document development activities, and ensure CRA performance. You will coordinate external and internal outreach to boost...
- ...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
$91.34k - $114.17k
...Clinical Research Associate - Oncology - 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...Work experience placementLocal areaVisa sponsorshipFlexible hours$91.34k - $114.17k
...Clinical Research Associate - Early Stage 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...Work experience placementRemote workFlexible hours$70 - $75 per hour
...Sr. Field Clinical Research Associate Remote with Travel required in the North Central Region (ideally based out of Boston, MA or Philadelphia, PA) Hybrid role Compensation: $70 - $75 per hour ABOUT THE ROLE Our client, a leading life sciences company, is seeking a Sr....Hourly payContract workPart timeLocal areaRemote work- ...Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of... ...nationally for excellence in research! Job Summary: The Clinical Research Associate I works directly with a Clinical Research Coordinator,...Full timeWork at officeLocal area
- ...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...Full timeLocal areaRemote work
$140k - $165k
...unsolicited resumes or candidates from outside staffing agencies or recruiters. Primary Objective of Position The Senior Clinical Research Associate (Sr. CRA) is responsible for acting as a central point of communication between Puma and his/her allocated investigative...Full timeInterim roleWork at officeRemote workWork from homeHome officeMonday to FridayNight shiftWeekend workAfternoon shift- ...our team, you'll have access to groundbreaking biomedical research facilities and world-class medical education programs. We... ...outcomes. What will you be doing in this role? The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research...Local area
- Cedars-Sinai is seeking a Clinical Research Associate I to work with research teams at the Smidt Heart Institute. This position involves coordinating clinical studies, evaluating data, and ensuring compliance with research protocols. Applicants should have at least a high...
- Profound Research, a contract research organization focused on advancing vaccine trials, is seeking an Assistant Clinical Research Coordinator to support high‑volume vaccine studies at our site. You'll coordinate patient visits, scheduling, data collection, and study procedures...Full timeContract work
- Cedars-Sinai Medical Center is seeking a Clinical Research Associate I to work with the study team to coordinate and implement research projects. You will evaluate data from source documents, enter data into electronic systems, and assist with regulatory submissions to...
$80k - $130k
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 RDI runs sample collection studies...$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...Hourly payRemote work$60k - $140k
Job SummaryClinical Research Coordinators wanted at Medpace! Become a CRA and join our growing... ...an exciting home-based opportunity for clinical research professionals with at least two... ...experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our...Full timeContract workTemporary workWork at officeRemote workWork from homeFlexible hours$43 - $45 per hour
...has partnered with a biotech company looking for a temporary research associate to join the team on a temporary basis. We are looking for... ...Lab Services, we offer solutions to help start, grow, and run clinical laboratories. Our recruiting team has over 21 years of proven...Permanent employmentContract workTemporary workLocal areaMonday to FridayShift work- ICON Strategic Solutions is seeking a Clinical Research Associate to support sponsor-driven trials globally. You will conduct site qualification, initiation, monitoring and close-out visits, ensuring protocol compliance and patient safety throughout the trial lifecycle....
- UCLA Health in Los Angeles is seeking a Staff Research Associate to support clinical research studies focused on gastroenterology and related conditions. You will collect and manage research data, maintain study databases, and prepare reports under the PI and senior staff...
$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...Contract workRemote work- Medasource is seeking a Sr. Field Clinical Research Associate for a remote, travel-based, part-time 12-month contract focused on the North Central Region. Hybrid role with monitoring responsibilities to ensure GCP compliance and study protocols across sites. The candidate...Remote jobContract workPart time
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