Clinical Research Associate, Sponsor Dedicated
Location: Canada; Remote
R1358062
When you join IQVIA as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development.
With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
- Full Time
- Level: Entry-level, Mid-level, Senior-level
- Travel: Yes
Success profile
What makes sponsor-dedicated CRAs at IQVIA successful? Check out the top traits we’re looking for and see if you have the right mix.
- COLLABORATIVE
- DETAIL-ORIENTED
- COMMUNICATOR
- INDEPENDENT
- CURIOUS
- PROBLEM-SOLVER
Explore this
career path
As you grow your CRA career at IQVIA, you’ll play an important role in helping our customers drive healthcare forward and impact the lives of patients around the world.
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CRA 1
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CRA 2
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Senior
CRA 1 -
Senior
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Senior
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What you
can expect
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Professional Development
Resources that promote your career growth
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Work-Life Balance
Leaders that support flexible work schedules
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Growth Potential
Clear pathways to success
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Collaboration
Teams that work together to achieve common goals
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Variety
Dynamic work environments that expose you to new experiences
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Best-in-class Training
Programs to help you build knowledge and gain skills
Clinical Research Associate, Sponsor Dedicated
Job description
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
- Supporting the development of a subject recruitment plan
- 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 and at least six 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
- Ability to speak English and French fluently
If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team.
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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 https://jobs.iqvia.com
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