Senior CRA, Sponsor Dedicated

IQVIA is a leading global provider of contract research services, advanced analytics and technology solutions to the life sciences industry formed through the merger of IMS Health and Quintiles.

On behalf of our local Clinical FSP department we are currently looking to further strengthen our team by hiring a Senior CRA that will exclusively take care one sponsor, a major global player with extensive pipeline within Oncology and Diabetes, among other therapeutic areas.

The role can be home-based or office based, with an average of 5/8 visits per month (both on-site and remote).

Why should you apply?

• You'd join a global team of 75.000+ brave minds

• In 2019 we completed almost 4.000 recruitment processes internally; once you join us, not even the sky is the limit

• We've been nominated a top 500 company every year since our inception in 2016

• FLEXJOBS awarded us the 9th spot in the top 100 Companies for Remote Jobs in 2021

• Forbes sees us as one of the dominant companies for the years to come - https://www.forbes.com/sites/jonmarkman/2020/10/30/iqvia-killing-it-in-the-drug-trials-business/?sh=5ca8f1963d21

Essential Functions of a Clinical Research Associate

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• 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.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• 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.
• Collaborate and liaise with study team members for project execution support as appropriate.

Qualifications

• Bachelor's Degree Degree in scientific discipline or health care, ideally
• At least 3 years of independent on-site monitoring experience
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of English language and Hungarian language.

#CRASDAJD

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 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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.