Clinical Research Associate, Single Sponsor dedicated in POLAND
Location: Warsaw, Poland; Poland; Remote
R1416180
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
CRA 2 -
Senior
CRA 3
Quote
“IQVIA empowers you to drive your own path within the organization. As no person’s route is the same and the clinical research landscape is forever changing, you are encouraged to continually seek career growth opportunities and to align your interests with your career goals.”
Lauren, Senior Clinical Research Associate 2
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, Single Sponsor dedicated in POLAND
Job description
IQVIA is hiring Clinical Research Associates!
Join IQVIA today and make an impact on patients’ outcome!
Job Overview
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.
Responsibilities
- 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
Qualifications
- A Bachelor's degree in a health care or other scientific discipline or educational equivalent
- Experience in on-site monitoring of clinical trials
- Alternatively, you should have an equivalent combination of education, training and experience
- Written and verbal communication skills including good command of Polish and English language
Connect to great opportunity™
IQVIA™ is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.
#weareIQVIA #projectpatientfocus #LI-Remote #CRASDAJD #CRA
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. Learn more at https://jobs.iqvia.com
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