Clinical Research Associate

1 week ago

Reading, Reading, United Kingdom IQVIA Argentina Full time

At IQVIA, we are seeking a highly skilled Clinical Research Associate to join our team. As a key member of our Clinical Research team, you will play a critical role in ensuring the successful delivery of clinical trials.

Key Responsibilities:

  1. Assist Clinical Research Associates and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems, ensuring accurate tracking of site compliance and performance within project timelines.
  2. Collaborate with Clinical Research Associates and Regulatory and Start-Up teams on the preparation, handling, and distribution of Clinical Trial Supplies and maintenance of tracking information.
  3. Coordinate the tracking and management of Case Report Forms, queries, and clinical data flow.
  4. Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
  5. Provide mentorship and training to less experienced Clinical Trial Assistants.
  6. Assist with the onboarding of new Clinical Trial Assistants.
  7. May accompany Clinical Research Associates on site visits to assist with clinical monitoring duties upon completion of required training.
  8. May participate in departmental quality or process improvement initiatives.

Requirements:

  1. Knowledge of applicable clinical research regulatory requirements.
  2. Minimum 6 months clinical research experience preferred.
  3. Proficiency in Microsoft Word, Excel, and PowerPoint.
  4. Effective written and verbal communication skills, including a good command of the English language.

We are a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. Our mission is to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.

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