(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 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- ...dedicated individual for a full-time position in Parsippany, United States, focused on site monitoring and management within clinical research. You will conduct site visits, ensure adherence to study protocols, and evaluate site practices in compliance with regulations...SeniorFull time
- IQVIA is seeking a Senior Clinical Research Associate 1 to monitor sites and ensure protocol adherence across oncology, cardiovascular, renal, metabolic, and more. This full-time role is based in the United States and requires on-site monitoring experience. You will conduct...SeniorFull time
$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...SuggestedFull timePart timeWork at officeLocal areaImmediate startWorldwide$87.2k - $182k
...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...SuggestedFull timePart timeLocal 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
$74.5k - $197.5k
...Tampa, FL, United States of America Salt Lake City, UT, United States of America Full time R1573716 Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively...Full timePart timeWork at officeImmediate startWorldwide- ...pharmaceutical company based in Morristown, New Jersey, is hiring a Clinical Research Associate to oversee clinical trial activities across multiple study... ...support Job Type: Full-Time | Work Type: On-Site | Industry: Pharmaceutical | Experience: Mid-Senior...Full timeInterim roleWork at office
$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- Barclays is seeking a Director-level software engineering leader in New Jersey to drive technical excellence. You will design scalable, maintainable software, mentor engineers, and align technical decisions with business goals across cross-functional teams. You will shape...Senior
- Ferring Pharmaceuticals SA seeks a Senior Principal Statistician in Biostatistics to lead statistical input for clinical development and evidence generation. You will integrate real-world and trial data, contribute to regulatory submissions, and guide lifecycle strategies...Senior
- ...Job Title Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities: Participate and...
- An ideal candidate for our Clinical Project Associate position is an individual who can prioritize and multitask, is experienced in windows-based computer applications, and possesses strong communication skills. The right individual will have strong time management skills...
$150k - $350k
...Job Description:We are seeking an experienced Cost Segregation Senior Manager/Principal to join our growing Forensic & Valuation... ...the appropriateness and benefits of cost segregation services.Researching and documenting applicable tax laws, regulations, and IRS guidance...SeniorFull timeLocal area$32.5 - $36 per hour
Job Description Overview\n Intuit is seeking highly motivated individuals to join our dynamic team as dedicated year-round TurboTax Retail Experts in one of our TurboTax Retail or Flagship locations across the United States. This unique opportunity combines tax expertise...SeniorLocal area$191k - $225k
...Built on a 70-year plus commitment to science and research, Ferring is relentless in its pursuit of... ...up to the world’s oldest enemy: disease. As a Senior Principal Statistician, Biometrics you will be part of clinical development teams, contributing to the design,...SeniorFull timeTemporary workLocal areaFlexible hours- Company DescriptionTop 20 Regional Public Accounting FirmJob DescriptionPUBLIC AUDITORS- STAFFS & SENIORS!Top 25 CPA firm founded in 1940 is opening a new office in Northern NJ and is seeking Public Auditors at all levels!! Gain experience with clients of all sizes and...SeniorWork at office
- ...DescriptionExpanding service firm located in Morris County, NJ.Job DescriptionExpanding service firm in Morris County, NJ is seeking a Senior IT Auditor with the CISA certification. Responsibilities include determining audit scope/objectives based on risk assessment,...Senior
- Job ID: 29241393Reference Number: 26-00930Title: Senior Java Microservices EngineerPosted Date: 2026-09-10Contact: Mahi MahiContact Email: ****@*****.*** Phone: (***) ***-****Company: HAN Staffing Job Titles: Senior Java Microservices Engineer Location...Senior
$70k - $85k
...efficiency initiatives in various areas of the Sales organization as needed.• Provide analytical support and other ad-hoc analysis to senior management and department managers as needed.QualificationsRequirements:• 5+ years of budget, forecasting and financial analysis...Senior- Canfield Scientific, Inc. is seeking a Clinical Services: Clinical Project Associate to provide project management and operational support to designated clinical project teams, ensuring quality, timelines, and specifications are met. The role involves document management...Work at office
- Canfield Scientific, Inc. is seeking a Clinical Project Associate in Parsippany, New Jersey. The role involves coordinating clinical project activities, maintaining study documentation, and supporting data management to ensure timely, high-quality study deliverables. The...Hourly payWork at office
- ...the month-end close Assist with the annual audit process including the draft of the financial statements and related notes Research and analyze expense variances for company management Accounting for fixed income, equities, other investments. Qualifications...Senior
- Canfield Scientific, Inc. in New Jersey is seeking a Clinical Projects Associate to support clinical project teams with documentation, data management, and timely execution of study activities. The role emphasizes multitasking, strong communication, and proficiency in Windows...Work at office
- Canfield Scientific, Inc. is seeking a Clinical Project Associate who can prioritize, multitask, and communicate clearly in a fast-paced environment. The role supports designated clinical project teams with quality, timelines, and project specifications, and involves document...Work at office
- Canfield Scientific, Inc. is seeking a Clinical Project Associate to provide project management and operational support for designated clinical projects. The role involves ensuring quality, timelines, and project specifications are met, while aiding in documentation and...Work at office
$85k
...+ years corporate or agency recruiting experience• Some supervisory experience• Experience with Applicant Tracking Systems Additional Information$85K plus bonus SummaryType: Full-timeFunction: Human ResourcesExperience level: Mid-Senior LevelIndustry: Consumer ServicesSenior$100k
...preferred.Knowledge of TeamMate, ACL, Business Objects, or other data analytics tools are preferred.Additional Informationup to $100K ****@*****.***: Full-timeFunction: Information TechnologyExperience level: Mid-Senior LevelIndustry: Consumer GoodsSenior- ...Travel required.All work to be performed onsite in Parsippany.3 – 6 yrs. relevant experience with Bachelor's Degree, 5+ yrs. with Associate's Degree;Good working knowledge of dissolution and reverse phase HPLC is necessary and a requirement.Working knowledge of both computer...
- ...a globally recognized FORTUNE 500 industrial manufacturing organization whose flagship manufacturing campus is actively seeking a Senior Engineering Manager. Reporting to the VP/General Manager, this candidate would assume ownership over an 40+ employee department while...SeniorFull time
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