CRA 2/Senior CRA 1
$90.2k - $175.1kIQVIA
Durham, North Carolina, United States of America Columbia, Maryland, United States of America Phoenix, AZ, United States of America Gilbert, AZ, United States of America San Francisco, CA, United States of America Annapolis, MD, United States of America Chicago, Illinois, United States of America Glendale, AZ, United States of America New York, NY United States of America Sacramento, CA, United States of America Houston, Texas, United States of America Indianapolis, IN, United States of America Rockville, Maryland, United States of America Carlsbad, CA, United States of America Dallas, Texas, United States of America Full time
R1547445
Join a Team That’s Advancing Clinical Research We’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 Do Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in accordance with GCP/ICH guidelines Build strong relationships with investigative sites to drive performance, recruitment, and engagement Ensure protocol compliance, data integrity, and high-quality study execution Proactively identify risks, resolve issues, and escalation when needed Track and manage study progress, including regulatory approvals, enrollment, and data quality Maintain accurate documentation and contribute to inspection readiness Collaborate with cross-functional teams to ensure successful study delivery What You Bring Bachelor’s degree in life sciences, healthcare, or related field (or equivalent experience) 1.5+ years of on-site monitoring experience Solid understanding of GCP, ICH, and regulatory requirements Strong communication, problem-solving, and organizational skills Ability to manage multiple priorities in a fast-paced environment Why Join Us Make a direct impact on advancing clinical research and improving patient outcomes Work alongside experienced, collaborative teams Opportunities for growth and career development Dynamic, fast-paced environment where your contributions matter IQVIA 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled #J-18808-Ljbffr IQVIA$90.2k - $175.1k
...looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical... ...sciences, healthcare, or related field (or equivalent experience) 1.5+ years of on-site monitoring experience Solid understanding of...SeniorFull timePart timeImmediate startWorldwide- IQVIA Argentina in Gilbert, United States, is looking for passionate Clinical Research Associates (CRA 2 and Sr. CRA 1) with onsite monitoring experience in oncology to join our team. You'll ensure high-quality clinical trials by building relationships with investigative...Senior
- IQVIA in Gilbert, AZ is seeking a Clinical Research Associate (CRA) to partner with investigative sites and cross-functional teams to deliver... ...bachelor’s degree in life sciences or related field and at least 1.5 years of on-site monitoring experience, with strong...Senior
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$90.2k - $175.1k
IQVIA is seeking a Clinical Research Associate (CRA) with experience in oncology for an onsite role in Gilbert, Arizona. The successful candidate will monitor clinical trials, ensuring compliance and high-quality execution, while collaborating with investigative sites....Senior- Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CRA) for CNS/Psychiatry with a West Coast remote work setup. You will manage sites across studies, perform initiation visits, and ensure regulatory compliance while coordinating with teams. A 4-year...SeniorRemote jobWorldwide
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$97k - $193k
Worldwide Clinical Trials Holdings, Inc. is looking for an experienced Clinical Research Associate (CRA) to manage research activities across various therapeutic areas. This role requires a minimum of 5 years of CRA experience and a relevant university or Nursing degree...SeniorWorldwide- Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Research Associate (CRA) to oversee research activities at clinical sites. The CRA will manage all stages of clinical studies, from identifying potential sites to closing down research activities when studies...SeniorRemote jobWork at officeWorldwide
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$130k - $133k
...South Dakota, North Dakota, Minnesota, Wisconsin, Iowa, Missouri, Arkansas, Louisiana, Illinois, Michigan, Indiana Job Overview The Senior CRA II is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or...SeniorWork at officeLocal areaWork from homeNight shift- ICON Strategic Solutions is seeking a Senior Clinical Research Associate focusing on Cardio (Smartpulse A-fib) to support studies in the cardiovascular/ electrophysiology space. This role requires 3 years of monitoring experience and a bachelor’s degree in life sciences...Senior
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$70k - $75k
...performance, and assist with volume by sweeping Tier 1 for aging and complex tickets.... ...Collaborate with the Support Desk Manager and Tier 2 Lead to uphold SLAs Document fixes and... ...within a forward-thinking IT team Seniority level Seniority level Mid-Senior level Employment...SeniorFull timeRemote work$168k - $240k
...evolution of Slalom.The Role: M&A Principal/Senior PrincipalWhat You’ll Do:* Delivery areas... ...information in this posting, please contact us at: [1] ****@*****.***. EEO and... ...advise the talent acquisition team or contact [2] ****@*****.*** if you require...SeniorTemporary workWork at officeLocal areaImmediate start- IQVIA Argentina is seeking a Clinical Research Associate (CRA) in Phoenix, USA. In this role, you'll lead site monitoring visits and ensure... ...candidates have a Bachelor's degree in life sciences and at least 1 year of monitoring experience. Join a team making a direct impact...Senior
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