(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
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...SeniorFull timePart timeImmediate 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$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$97k - $193k
...Senior Clinical Research Associate position supporting psychiatric and CNS clinical trials at investigative sites across the Central United States. Role involves site management, monitoring visits, regulatory compliance oversight, and collaboration with study teams to...SeniorInterim role$90.2k - $175.1k
...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$71.9k - $189k
...IQVIA seeks a Senior Clinical Research Associate to oversee oncology trial sites, ensuring protocol compliance and regulatory adherence. The role involves site monitoring, recruitment support, training, and quality assurance for Phase 1 cancer studies across multiple...SeniorWork at office$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 MonitorPerform 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
$87.2k - $182k
...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...Full timeWork at office- ...values of the organization and ensures Laboratory employees do the same Requirements Education / Certifications: ~ Associates degree in Medical Laboratory Science is accepted. ~ Bachelor's degree is preferred. ~ Appropriate certification based on...Senior
$35.8k - $123k
...United States of America Carlsbad, CA, United States of America Full time R1568247 Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e...Full timePart timeImmediate startWorldwide$20 - $25 per hour
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$38.06 per hour
...throughout the region so that we can improve the lives of children beyond the walls of our hospital. Overview The Clinical Research Associate III is designed to facilitate the research for faculty investigators. The position is necessary to maintain and enhance overall...Full timeWork experience placementSeasonal work- ...Senior Product Designer Lead the design of thoughtful, scalable digital experiences that are rooted in user needs, aligned with business... ...-to-end product design from discovery to delivery Translate research and insights into actionable experiences (via an experience...Senior
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$90.2k - $190k
...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$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$74.5k - $197.5k
...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$74.5k - $197.5k
...IQVIA seeks experienced Clinical Research Associates II and Senior Clinical Research Associates to oversee clinical trial sites across multiple therapeutic areas nationwide. The role involves managing all phases of site monitoring, ensuring protocol compliance, regulatory...Work at office- ...HNTB is seeking a senior engineering technology leader to serve as the enterprise owner for select engineering technologies, guiding the technology lifecycle from evaluation to deployment and governance. You will champion technology adoption across projects, disciplines...Senior
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