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IQVIA fournit des données, des technologies, du conseil et des services de recherche clinique aux acteurs de la santé et des sciences de la vie.

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Description de l’offre

The Senior Clinical Data Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met. Summary of the Essential Functions of the Job

  • Perform ongoing data review, including reconciliation of third party data streams and serious adverse event reconciliation with the safety database.
  • Perform User Acceptance Testing (UAT) of clinical databases.
  • Perform Quality Control (QC) of clinical databases.
  • Perform ongoing updates of Data Management-related documentation, as needed. Minimum

Requirements

Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution (i.e. RN, MT, PA, RT) is preferred, but individuals with commensurate experience will be considered. - Minimum of 3 years of data management experience is required. - Experience with Electronic Data Capture (EDC) system(s) is required- Oracle Inc.'s Inform™ EDC system is preferred. - Oncology and/or inflammatory therapeutic area experience This role is not eligible for UK visa sponsorship 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 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete.

Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Prérequis

  • ICH
  • Good Clinical Practices (GCP)
  • Oncology and/or inflammatory therapeutic area experience