Offer summary

Qualifications:

MSc and/or BSc in Health Sciences or related field., Proficient in Czech and English languages., Minimum of 1 year experience as a Clinical Research Associate (CRA)., Familiarity with ICH-GCP guidelines and experience with CTMS, eTMF, and EDC systems..

Key responsabilities:

Conduct site visits including selection, initiation, monitoring, and close-out according to ICH-GCP guidelines.

Support patient recruitment efforts at the site(s).

Manage RCA and CAPA processes, and report on study progress.

Document findings in Monitoring Visit Reports and manage study documents in eTMF.

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures. To learn more, visit www.iqvia.com.

Job description

CRA - Czech Republic - One Sponsor- Homebased

Would you like to be one of us? Are you eager to change and achieve new steps in your professional career?

IQVIA is looking for a Clinical Research Associate to provide service to one of our sponsors.

You would be responsible for:

Performing visits (such as selection, initiation, monitoring and close-out) according to ICH-GCP guidelines.
Support of the site(s) i.v.m. patient recruitment.
RCA and CAPA management.
Reporting of visits and progress of the studies.
Management and archiving of study documents in eTMF.
Collaboration with the project/study team.
Documentation in Monitoring Visit Reports and follow-up letters.

We are looking for:

MSc and/or BSc education level. Preferable in Health Sciences.
Proficient level of Czech and English.
Good knowledge and application of ICH-GCP.
Minimum of 1 year of experience as a CRA.
Experience in using CTMS, eTMF and EDC systems.
Experience in different studies, phases, visits and therapeutic indications.
Passion for science, helping patients and collaborating with the sites.
Availability to travel across the country, driving license.

#CRASDAJD #LI-ANAHDEZCIP

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.

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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