Clinical Research Associate
$91.34k - $114.17kICON Strategic Solutions
Clinical Research Associate - Multi Therapeutic Area (Early Development) - West Region 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 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 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. #J-18808-Ljbffr
$71.9k - $189k
...Clinical Research Associate, Sponsor Dedicated California, United States of America | Full time | Field-based | R1541733 To be eligible for this position, you must reside in the same country where the job is located. Essential Functions Perform site monitoring visits (...SuggestedFull timePart timeLocal areaImmediate startWorldwide- ...We are looking to add a Clinical Research Associate to a growing team to help monitor an Oncology trial. This role will start around 20-25 hours weekly with the potential to increase to full time toward the beginning of 2027. This study will need mostly remote support...SuggestedFull timeLive inLocal areaRemote work
- ...Responsibilities Manage day-to-day operational execution of assigned clinical studies to achieve study milestones, quality expectations, and... ...credentials preferred. Typically requires 5+ years of clinical research or pharmaceutical industry experience, including 2+ years of...Suggested
- ...Direct message the job poster from Integrated Resources, Inc ( IRI ) Lead Recruiter at Integrated Resources Inc. (IRI) Sr Clinical Research Spec 100% remote in CA/MN 12 Months+ Preferred location(s): Santa Rosa, CA / Northern California - Bay Area / Plymouth,...SuggestedContract workRemote work
$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Southern California 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...SuggestedWork experience placementInterim roleLocal areaRemote workFlexible hours$109.5k - $153.3k
...goals in alignment with corporate goals. Organize and maintain clinical study documentation (e.g., Trial Master Study Files) including... ...laboratory technology preferred. Minimum of five (5) years of clinical research monitoring experience (including pre-study, initiation, routine...For contractorsLocal areaRemote work$110.52k - $138.15k
...Sr. Clinical Research Associate - West Coast 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- ...We are hiring in Chicago, Southern California & NY (Northeast). Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry‑leading performance...Contract workTemporary workLocal areaRemote work
$90k - $130k
...FL, GA, KS, MA, MD, MI, NC, OH, OK, TN, TX, WA Vanguard Clinical, Inc. is a Contract Research Organization (CRO) headquartered in San Diego, CA. Our... ...clinical data at assigned sites. The Clinical Research Associate (CRA) will execute monitoring responsibilities for clinical...Permanent employmentFull timeContract workInterim roleWork at officeRemote workFlexible hours- ...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
- ...We are looking for a FREELANCE, PART-TIME CRA to strengthen our clinical operations team in Ventura, Illinois & Ohio! Job Requirements... ...of onsite monitoring activities Profound knowledge of clinical research processes and medical terminology Expert knowledge of ICH GCP,...Part timeFreelanceLocal areaRemote work
- ...investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conduct the clinical study throughout the study period. Trains investigational site staff as necessary When applicable, supports preparation of...Interim roleRemote work
- ...A renowned clinical research organization in California is looking for a Clinical Research Associate to oversee monitoring activities for clinical sites. Responsibilities include conducting various types of monitoring visits, preparing monitoring reports according to regulatory...Local areaRemote work
- 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...Local area
- IQVIA Argentina is seeking a Clinical Research Associate to provide on-site monitoring and ensure adherence to clinical and regulatory standards. Candidates must have at least 2 years of experience and a Bachelor's degree in a relevant field. The role involves collaborating...
- ICON Strategic Solutions is seeking a Clinical Research Associate for the West Region to serve as the primary contact between investigational sites and the sponsor. The ideal candidate will have a Bachelor’s degree in Life Sciences and 2+ years of on-site monitoring experience...
- Cedars-Sinai Medical Center in California is seeking a Clinical Research Associate I to support the coordination and implementation of noncomplex research studies. This role involves assisting in various tasks such as data collection, prescreening potential participants...Local area
- BoneSource is looking for a Clinical Research Associate I to assist in tasks supporting noncomplex research studies under the direction of supervising staff. Responsibilities include data collection, prescreening participants, and ensuring compliance with guidelines. The...
- Direct Jobs is seeking a Clinical Research Associate I in California, Missouri, to assist with the coordination and implementation of noncomplex research studies. Key responsibilities include collecting and evaluating data, scheduling research participants, and assisting...
- Job Description Join our team and use your skill with an organization known nationally for excellence in research! The Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising...Daily paidLocal area
- Initial Therapeutics, Inc. is looking for a Clinical Research Associate to join our team in California. The role involves ensuring effective site engagement and maintaining regulatory compliance in clinical trials. You will be the main point of contact for investigative...
$90k - $130k
A leading clinical research organization is seeking a Clinical Research Associate to manage clinical sites and monitor data for trials. The ideal candidate should have at least 2 years of experience in clinical monitoring and a strong understanding of ICH/GCP guidelines...Remote job$93.6k - $114.4k
...Clinical Trial Assistant W2 Contract-to-Hire Salary Range: $93,600 - $114,400 per year Location: Redwood City, CA - Hybrid Role Base pay... ...industry, preferably in Clinical Operations or Clinical Research related experience. Familiar with Phase I Healthy Volunteer studies...Contract work$46 per hour
...Job Description Job Title: Clinical Trials Project Assistant II Type: Contract - 6 Months Pay: $46.00/hr Location: 333 Lakeside Drive, Foster City, CA FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations Position Overview Clinical Operations is responsible...Extra incomeContract workWork experience placementWork at officeWorldwideFlexible hours- A healthcare staffing agency is seeking a Clinical Trial Assistant for a hybrid role in California. This entry-level position offers an... ...relevant degree and 0-3 years of experience in clinical operations or research. A proactive, detail-oriented approach is essential. #J-18808-...
- ...JOB SUMMARY: The Farm Technician works in cooperation with the Farm Manager and the Research Trials Manager to improve the growing conditions of the research crops. Farm Technician is primarily responsible for supporting daily farm operations and assisting with irrigation...Seasonal workWork at office
$68.5k - $90k
...Departments of Biochemistry, Plant Pathology and Microbiology, and the Center for Conservation Biology. Use your skills as an experienced research administrator to independently develop and coordinate research proposals for an assigned portfolio of Principal Investigators....Contract workFor contractorsWork visa$83k - $86k
...JOB SUMMARY Uses skills as a seasoned, experienced research administrator to independently monitor, reconcile, and manage research funding from a variety of sources, including sponsored awards, gifts, and other non-sponsored funding, in compliance with UC, institution...Full timeTemporary workFor contractorsSummer workWork at officeRemote workWork from homeShift work$34.17 - $37.77 per hour
...Position Information Uses skills as an experienced research administrator to independently develop and/or oversee research proposals, awards and/or transactions related to contract and grant management and maintain contract and grant records in compliance with institutional...Hourly payContract workFor contractorsLocal areaWorldwideWork visa$45.84 per hour
...withdrawn. Requirements Graduate from a medical laboratory technician training program accredited by the National Accrediting Agency for Clinical Laboratory Sciences (NAACLS) OR the Accrediting Bureau of Health Education Schools (ABHES) OR educational program acceptable to...Hourly payContract workWork at officeLocal areaShift workDay shift
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