Clinical Research Associate
5 months ago
Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone - you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.
- Award winning and innovative, we’ll give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You’ll be building a smart and flexible career with no limits.
- While projects vary, your typical responsibilities might include:
- Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
- Establishing regular lines of communication plus administering protocol and related study training to assigned sites
- Evaluating the quality and integrity of site practices - escalating quality issues as appropriate
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.
- You should have:
- A Bachelor's degree in a health care or other scientific discipline or educational equivalent
- Successful completion of a CRA Trainee Program or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred.
- Alternatively, you should have an equivalent combination of education, training and experience
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
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Associate Clinical Research Associate
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Clinical Research Associate
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Clinical Research Associate
2 months ago
Kirkland, Quebec, Canada IQVIA Full timeJob DescriptionOverviewIQVIA is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for conducting clinical trials, monitoring site progress, and ensuring compliance with clinical best practices.Key ResponsibilitiesParticipate in investigator recruitment and on-site evaluation...
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Clinical Research Associate II
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Clinical Research Associate II
4 weeks ago
Kirkland, Quebec, Canada IQVIA Full timeJob Title: Clinical Research Associate IIIQVIA is seeking a highly skilled Clinical Research Associate II to join our team in Eastern Canada. As a key member of our clinical research team, you will be responsible for monitoring and managing clinical trials in the oncology field.Key Responsibilities:Conduct site evaluation visits to assess the capability of...
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Clinical Research Associate II
2 weeks ago
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Clinical Research Associate II
2 weeks ago
Kirkland, Quebec, Canada IQVIA Full timeJob Title: Clinical Research Associate IIIQVIA is seeking a highly skilled Clinical Research Associate II to join our team in Eastern Canada. As a key member of our clinical research team, you will be responsible for monitoring and managing clinical trials in the oncology field.Key Responsibilities:Conduct site evaluations, initiation, and interim close-out...
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Kirkland, Quebec, Canada IQVIA Full timeJob Title: Clinical Research Associate II Oncology MonitoringAbout the Role:IQVIA is seeking a highly skilled Clinical Research Associate II to join our team in Eastern Canada. As a Clinical Research Associate II, you will be responsible for monitoring and managing clinical trials in the oncology field.Key Responsibilities:Conduct site evaluation visits to...
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Clinical Research Associate II
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Clinical Research Associate II
4 weeks ago
Kirkland, Quebec, Canada IQVIA Full timeJob Title: Clinical Research Associate II - Oncology MonitoringIQVIA Biotech is seeking a highly skilled Clinical Research Associate II with oncology monitoring experience based in Eastern Canada. The ideal candidate will be bilingual in French and English and possess a strong understanding of Good Clinical Practices (GCP) and clinical trial management.Key...
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Clinical Research Associate II
2 months ago
Kirkland, Quebec, Canada IQVIA Full timeJob SummaryIQVIA is seeking a highly skilled Clinical Research Associate II to join our team in Eastern Canada. As a Clinical Research Associate II, you will be responsible for monitoring and managing clinical trials in the oncology field. This is an exciting opportunity to work with a leading global provider of advanced analytics, technology solutions, and...
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Clinical Research Associate II
1 week ago
Kirkland, Quebec, Canada IQVIA Full timeJob DescriptionIQVIA Biotech is seeking a highly skilled Clinical Research Associate II to join our team in Eastern Canada. As a Clinical Research Associate II, you will be responsible for monitoring and managing clinical trials, ensuring compliance with Good Clinical Practices and regulatory requirements.Key ResponsibilitiesConduct site evaluation visits to...
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Clinical Research Associate
1 month ago
Kirkland, Quebec, Canada IQVIA Full timeJob DescriptionAs a Clinical Research Associate at IQVIA, you will play a critical role in the preparation and execution of Phase I to IV clinical trials. Your responsibilities will include overseeing the progress of clinical investigations, conducting interim site assessment, initiation, and closure visits, and monitoring clinical trials in accordance with...
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Clinical Research Associate
1 month ago
Kirkland, Quebec, Canada IQVIA Full timeJob DescriptionAs a Clinical Research Associate at IQVIA, you will play a critical role in the preparation and execution of Phase I to IV clinical trials. Your responsibilities will include overseeing the progress of clinical investigations, conducting interim site assessment, initiation, and closure visits, and monitoring clinical trials in accordance with...
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