(Senior) Clinical Research Associate
$90.2k - $175.1kIQVIA
Join a Team That’s Advancing Clinical ResearchWe’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and patient focus.What You’ll DoLead and execute site monitoring visits (selection, initiation, routine, and close-out) in accordance with GCP/ICH guidelinesBuild strong relationships with investigative sites to drive performance, recruitment, and engagementEnsure protocol compliance, data integrity, and high-quality study executionProactively identify risks, resolve issues, and escalate when neededTrack and manage study progress, including regulatory approvals, enrollment, and data qualityMaintain accurate documentation and contribute to inspection readinessCollaborate with cross-functional teams to ensure successful study deliveryWhat You BringBachelor’s degree in life sciences, healthcare, or related field (or equivalent experience)1.5+ years of on-site monitoring experienceSolid understanding of GCP, ICH, and regulatory requirementsStrong communication, problem-solving, and organizational skillsAbility to manage multiple priorities in a fast-paced environmentWhy Join UsMake a direct impact on advancing clinical research and improving patient outcomesWork alongside experienced, collaborative teamsOpportunities for growth and career developmentDynamic, fast-paced environment where your contributions matterIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is $90,200.00 - $175,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.SummaryLocation: Durham, North Carolina, United States of America; Overland Park, KS, United States of America; Parsippany, New Jersey, United States of America; Carlsbad, CA, United States of AmericaType: Full time
$90.2k - $175.1k
IQVIA is now hiring for a Senior Clinical Research Associate located on the West Coast, US to join our growing Early Clinical Development team working exclusively in Phase I.Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play...SeniorFull timePart timeImmediate startWorldwide$71.9k - $189k
Job Overview:Join our dynamic team as a Clinical Research Associate! You’ll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking cancer...SeniorFull timePart timeWork at officeLocal areaImmediate startWorldwide$74.5k - $197.5k
...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.• i.e., Good Clinical Practice (GCP) and...SeniorFull timePart timeLocal areaImmediate startWorldwide- ...Senior Clinical Research Associate IQVIA is now hiring for a Senior Clinical Research Associate located on the West Coast, US to join our growing Early Clinical Development team working exclusively in Phase I. Job Overview We are seeking a dedicated Clinical Research...SeniorImmediate start
$90.2k - $150.4k
...IQVIA Biotech seeks a Clinical Research Associate 2 to monitor clinical trial sites and ensure protocol compliance, regulatory adherence, and data integrity. The role involves site management across multiple visit types, staff training, enrollment tracking, and regulatory...SeniorFull time$71.9k - $189k
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...IQVIA seeks a Clinical Research Associate to lead site monitoring activities and ensure protocol compliance across clinical trials. The role involves partnering with investigative sites and cross-functional teams to execute studies to GCP/ICH standards while managing regulatory...Senior$90.2k - $197.5k
Role Overview: As a Clinical Research Associate, you’ll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research.Key Responsibilities:Site Visits: Conduct selection, initiation, monitoring...Full timePart timeWork at officeLocal areaImmediate startWorldwide- ...Clinical Research Monitor Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. • Perform site monitoring...Local area
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...Clinical Research Associate supporting sponsor-dedicated clinical trials across multiple U.S. locations. Responsibilities include site monitoring, protocol training, recruitment tracking, data quality oversight, and regulatory documentation management to ensure protocol...Work at office$74.5k - $197.5k
...Clinical Research Associate responsible for monitoring clinical trial sites and ensuring protocol compliance, regulatory adherence, and data quality. The role involves site visits, recruitment oversight, training, documentation management, and cross-functional collaboration...Work at office$71.9k - $169.3k
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...Responsibilities Update and maintain clinical documents and Trial Master Files to track site compliance and performance Prepare, handle, distribute, and archive clinical documentation according to standard operating procedures Track and manage Case Report Forms...- ...Sharp HealthCare is seeking a Clinical Documentation Improvement Specialist to perform concurrent review of medical records, issuing physician inquiries, and coordinating with medical staff to improve documentation quality. You will lead CDI initiatives, educate clinical...Senior
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...Clinical Research Associate role supporting sponsor-dedicated monitoring activities across multiple U.S. sites. Responsible for site management, protocol compliance, data integrity oversight, and regulatory documentation in accordance with GCP and ICH guidelines. Responsibilities...Work at office$90.2k - $175.1k
...Clinical Research Associate position supporting Phase I early clinical development trials across multiple US locations. The role involves conducting site visits, monitoring protocol compliance, managing enrollment, and ensuring data integrity while working with cross-functional...- ...Cisco Systems seeks a Senior Analog/Layout Engineer to architect physical blueprints for high-speed optical interconnects on the Silicon One platform. You will own block-to-top integration for 100G–400G lambda architectures, guiding from floorplanning through post-layout...Senior
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...Clinical Research Associate position focused on sponsor-dedicated monitoring and site management for clinical trials. Responsible for conducting site visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation across multiple study...Work at office- ...Our medical device client in Carlsbad is growing their finance team! We are seeking a Senior Accounting Manager / Cost Accountant, who will play a crucial role in managing and analyzing the financial aspects of our client's manufacturing operations. This position is responsible...SeniorFull time
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JLM Strategic Talent Partners is seeking a Contracts Manager in Carlsbad, CA, with 10-15 years of construction contract management experience. The successful candidate will lead commercial operations, liaise with designers and engineers, and manage the RFP/RFQ process....SeniorHourly payContract work- ...TaylorMade Golf seeks a Senior Digital Product Manager for Global eCommerce to own strategy, execution, and continuous improvement of its worldwide online business. You will lead a team, align roadmaps with regional needs, and collaborate with analytics to prioritise...SeniorWorldwide
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