This job posting may have expired!
Use our `search` to find similar offers.
Similar jobs

Contract and Regulatory Specialist - Single sponsor!

IQVIA Holdings Inc.

Tel Aviv, Israel

Essential Functions

  • Ensurethe successful negotiation and ongoing management of clinical trial agreements with investigative sites and vendor agreements and associated budgetmanagement.

  • Maintainaccurate records, metrics and reports; identify gaps and report to management; make recommendations for process improvement andefficiencies

  • accountabilityfor processes or groups of trials; operates with limitedoversight

  • Achievessuccessful delivery of site start-up, in-house site management and closeout activities meeting internal and external clientrequirements.

  • Responsibleforend to endprocess withincountry

Qualifications

  • Bachelor Degree in Economics or equivalent, preferebly.

  • At least 2 years of experience in Regulatory submissions.

  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.

  • Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.

  • Effective written and verbal communication skills including good command of English language.

  • Effective time management and organizational skills.

  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

  • Permanent position

  • Homebased

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.

Job posted: 2021-04-08

3