Clinical Research Associate, Sponsor Dedicated
$64k - $189kIQVIA
Clinical Research Associate, Sponsor Dedicated
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. Position requires 65-70% nationwide travel.
Essential functions include performing site monitoring visits, working with sites to drive subject recruitment, administering protocol and related study training, evaluating the quality and integrity of study site practices, managing the progress of assigned studies, creating and maintaining appropriate documentation, collaborating with study team members, and supporting development of project subject recruitment plan.
Minimum recruitment standards include 2.5 years of clinical research coordination experience at site level, nursing or university degree in one of the life sciences, knowledge of electronic data capture preferred, and equivalent combination of education, training and experience.
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.
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.
The potential base pay range for this role, when annualized, is $64,000.00 - $189,000.00. 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$64k - $189k
...IQVIA seeks an experienced Clinical Research Associate for sponsor-dedicated monitoring and site management across multiple U.S. regions. The role involves conducting site visits, managing study progress, ensuring regulatory compliance, and supporting recruitment and enrollment...Suggested- ...Clinical Research Associate, Sponsor Dedicated 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...SuggestedLocal area
$64k - $189k
...applicable regulations and guidelines, and sponsor requirements. Position requires 65-70%... ...and regulatory requirements, i.e., Good Clinical Practice (GCP) and International... ...RECRUITMENT STANDARDS:2.5 years of clinical research coordination experience at site level Nursing...SuggestedFull timePart timeLocal areaImmediate startWorldwide$90.2k - $190k
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...IQVIA seeks a Clinical Research Associate II to conduct on-site monitoring for clinical trials in therapeutic areas including CNS, cardiovascular, obesity, and NASH/MASH. The role involves site management, regulatory compliance, protocol training, and cross-functional...Work at office- ...Senior Clinical Research Associate for oncology studies at a global CRO. Manages research activities across participating clinical trial sites, from initiation through closeout, with a focus on regulatory compliance and safety reporting. Requires 5+ years CRA experience...Contract workWork at office
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