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Clinical Study Manager , Medical Devices (Scotland) - NCR (R1056141) in Glasgow, UK at IQVIA™

Date Posted: 1/11/2019

Job Snapshot

  • Employee Type:
  • Location:
    Glasgow, UK
  • Experience:
    Not Specified
  • Date Posted:
  • Job ID:

Job Description

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Position Description

Our Client requires an experienced individual to manage clinical studies and prepare and submit medical device clinical study documentation in line with relevant regulations.
Key responsibilities and duties will include;

• Manage medical device clinical studies in line with GCP and other relevant regulations
• Prepare and submit medical device clinical study documentation
• Communicate with all relevant parties (internal and external)
• Mentor and train department personnel

Required Experience

The ideal candidate will have excellent communication skills and the ability to manage multiple projects. They must have clear written and oral communication skills and be able to work to tight deadlines. The successful applicant will be a flexible team player with strong prioritisation skills and the ability to work with minimal supervision. They will also have a proven ability in clinical study set-up and management.

It is essential that the successful candidate is qualified to degree level in a relevant application, for example nursing or biology, and that they can use Microsoft Word, Excel and PowerPoint. They should be able to demonstrate knowledge of GCP and ISO 14155, and of the relevant regulations and country-specific clinical study requirements.

The following attributes are also essential;
• Previous experience in medical device clinical studies
• Experience of writing clinical study reports and submission documentation
• Experience of dealing with regulatory bodies and ethics committees for clinical studies
• Experience in a quality system environment

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™

Job ID: R1056141