Clinical Research Associate

1 week ago

Luton, Luton, United Kingdom Pharmiweb Full time
Key Responsibilities

We are seeking a skilled Clinical Research Associate to join our team. The successful candidate will be responsible for:

  • Assisting Clinical Research Associates and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems.
  • Collaborating with CRAs and RSU on the preparation, handling, and distribution of Clinical Trial Supplies.
  • Coordinating the tracking and management of Case Report Forms, queries, and clinical data flow.
  • Acting as a central contact for the clinical team for designated project communications and correspondence.
  • Providing mentorship and training to less experienced Clinical Trial Assistants.
Requirements

To be successful in this role, you will need:

  • Knowledge of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH).
  • Minimum 6 months clinical research experience, preferably in a similar role.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.
  • Effective written and verbal communication skills, with a good command of the English language.
About Us

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, improving patient outcomes and population health worldwide.

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