IQVIA

CRA 2, Sponsor Dedicated

Company
IQVIA
Location
Reading
Posted
09 Jun 2021
Closes
09 Jul 2021
Ref
R1214266
Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

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 one of our biggest and strongest partnerships at global level we are currently looking to further strengthen the monitoring team with a Clinical Research Associate that will work home-based (mainly) on Oncology, Diabetes and CNS trials.

Why should you apply and become part of our #bravemindset?

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

• In 2020 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

Essential Functions of a Clinical Research Associate (CRA)

• 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.
• 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) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH 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.

Qualifications

• Bachelor's Degree or Master's Degree, ideally in scientific discipline or healthcare
• 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)

• Minimum of 12/18 months of independent monitoring experience
• Written and verbal communication skills including good command of English language

 

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.

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