Clinical Research Associate, Sponsor Dedicated
Location: Durham, North Carolina; Overland Park, Kansas; Parsippany, New Jersey; San Diego, California
R1358053
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
• Provide site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
• Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Build awareness of features and opportunities of study to site.
• Collaborate and liaise with study team members for project execution support as appropriate.
#CRASDAJD
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
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
As the COVID-19 virus continues to evolve, IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status
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