Associate Lab Project Set Up Manager
IQVIA Holdings Inc.
Livingston, United Kingdom
5d ago

Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions.

With a relentless focus on quality and innovation, Q2 Solutions uses its global experience and scientific expertise to transform science and data into actionable medical insights that help customers improve human health.

A joint venture of IQVIA (formerly QuintilesIMS) and Quest Diagnostics, Q2 Solutions combines the best of each parent organization’s clinical trials laboratory services capabilities to fulfill its mission of treating each sample as if a life depends on it.

Q2 Solutions is one of the world's leading Central Laboratories. Through the breadth and depth of our services along with extensive therapeutic, scientific and analytics expertise, we help our customers navigate an increasingly complex healthcare environment.

The result is that we have helped develop or commercialize all of the top 50 best selling drugs.

The aim of Q2 Solutions is to provide full support for a vast variety of analytical techniques for samples collected from patients participating in clinical trials throughout the world.

Our Project Services Department, within our Central Laboratory, acts as the primary interface between the Central Lab and the client, to effectively manage expectations and provide a quality service in relation to clinical laboratory testing.

We currently have a vacancy for a Project Set-up Manager, a pivotal role within the Project Services Department.

The key duties and responsibilities of this role includes : -

  • Review of clinical study protocols to determine lab testing requirements as part of initial discussions with both the client and laboratory team
  • Management of client expectations during the initial, set-up phase to communicate progress, clarify outstanding actions and highlight potential risks
  • Maintain productive communications and collaborations with key internal departments (e.g. laboratory; kit building and sample receipt teams) to identify key areas for consideration during study set-up to enable smooth progression and timely shipment of clinical trial kits on both a regional and global level.
  • Working with the Laboratory and Scientific teams to define the analytical and technical aspects required to provide lab services for each protocol
  • Review of laboratory database design to ensure adherence to clinical study protocol requirements
  • Lead update of laboratory databases in line with protocol amendments submitted by sponsor teams during active phases of clinical trials
  • Applicants are expected to meet the following criteria :

  • Degree or equivalent in a scientific discipline. Advanced degree an advantage
  • Strong problem solving, communication, influencing and leadership skills
  • Excellent organisational, planning and prioritising skills
  • An ability to multitask on a daily basis is essential in addition to being proficient in standard IT software packages including Microsoft Office
  • Previous experience in an external customer serving environment is essential with previous Project Management experience desirable
  • Previous Pharmaceutical, central laboratory or related industry experience would be an advantage
  • 2020-07-16 00 : 00 : 00

    Report this job
    checkmark

    Thank you for reporting this job!

    Your feedback will help us improve the quality of our services.

    Apply
    My Email
    By clicking on "Continue", I give neuvoo consent to process my data and to send me email alerts, as detailed in neuvoo's Privacy Policy . I may withdraw my consent or unsubscribe at any time.
    Continue
    Application form