Clinical Research Associate
Location: Parsippany, New Jersey
R1251414
Take your therapeutic expertise to the next level and help drive the evolution of clinical development for a variety of sponsors.
As a Clinical Research Associate within our full-service model, you’ll have the opportunity to embrace your passion for a specific therapeutic
area and work with cutting-edge technology developed specifically for CRAs by CRAs. With access to world-class training and professional
development, we’ll give you the tools you need to create the career you want.
- Full Time
- Level: Entry-level, Mid-level, Senior-level
- Travel: Yes
Success profile
What makes CRAs aligned to our full-service model successful? Check out the top traits we're looking for and see if you have the right mix.
- ANALYTICAL
- ORGANIZED
- COMMUNICATOR
- PROBLEM-SOLVER
- FACILITATOR
- VERSATILE
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
CRA 2 -
Senior
CRA 3
Quote
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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Best-in-class Training
Programs to help you build your therapeutic knowledge
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Variety
Dynamic work environments that expose you to new experiences
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Growth Potential
Clear pathways to success
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Therapeutically Aligned
Protocols aligned to your expertise
Clinical Research Associate
Job description
Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
Candidates must reside in {Maine, Massachusetts, Maryland, New Hampshire, New Jersey, New York, Pennsylvania, Rhoda Island, Vermont, Washington D.C and Ohio}
As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™ , we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. 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 will 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 will 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.
Additional Description:
You should have:
- A Bachelor's degree in a health care or other scientific discipline or educational equivalent
- At least two years of on-site monitoring experience
- Alternatively, you should have an equivalent combination of education, training and experience
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 toapply now and join our team.
IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled'
We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™
#C1920
#CRAFSAJD
At IQVIA, 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. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.
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, Inc. provides reasonable accommodations for applicants with disabilities. Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at workday_recruiting@iqvia.com to arrange for such an accommodation.
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