Ref No.

QUO01068

Location

UK ~ Nottingham

Project Manager

Company Overview

Our growing and successful business comprises of over 850 talented individuals globally, in an environment where everybody counts and is instrumental to our success.  With state-of-the-art manufacturing and clinical facilities in the UK and USA, we deliver a full range of drug development solutions around the globe saving our clients both time and money.

People join Quotient Sciences because we are a respected member of the drug development world, specialising in delivering innovative solutions that integrate formulation development, real time GMP manufacturing and clinical testing and data sciences. We pride ourselves on the quality of our services and our engaged culture. We are passionate about helping our customers get new medicines to market.

The Role

Quotient Sciences has a fantastic career opportunity for an experienced Project Manager.  This role will be based in the Project Management department at our site in Nottingham.

Reporting to a Director Project Management, you will be responsible for day to day management and completion of complex customer projects encompassing all aspects of Quotient’s service offerings including pharmaceutical sciences, clinical conduct (healthy volunteer trials) and data sciences.

As the Project Manager, you will be expected to deliver service excellence for our customers across the globe. You will develop a project plan and lead a multifunctional project team to deliver that plan to time, cost and quality.

You will comply & adhere to GXP guidelines and regulations as required of this role, being the primary contact with the Sponsor from project initiation to operational close out for allocated projects.

Main tasks and responsibilities include:

  • Leading external and internal communications to ensure adherence to the project plan and ensure the project team has a depth of understanding of customer requirements 
  • Generating and/or reviewing key study documentation from project initiation to reporting
  • Monitoring and control of allocated project progress to time/quality/cost.
  • Ensuring any third party contracts needed to support are in place and ensuring appropriate oversight processes are adhered to
  • Supporting account management working with commercial colleagues to develop proposals that support our customers with the development of their drug development programmes
  • Management of study execution to ensure regulatory approvals, pharmaceutical development work, recruitment and screening of volunteers, clinical manufacturing, clinical operations and data sciences activities are delivered for customers
  • Participate in Sponsor monitoring visits and site visits as required
  • Oversight of the Investigator Site File and Trial Master File as required
  • Tracking of allocated projects in MS Project on a real time basis
  • Management of close out studies to ensure data queries, post-study reporting to the regulatory authorities, scientific review meetings and archiving are completed in a timely manner for allocated studies

The Candidate

The successful candidate will be a driven and talented individual who thrives in a fast paced, delivery driven environment. You will be qualified to at least degree level in a science subject and a have at least 2 years project management experience in a Clinical Research Organisation (CRO) or Contract Development Manufacturing Organisation (CDMO).  A good understanding of the drug development process is essential for this role.

Other skills and experience required:

  • Excellent project management, customer service, communication and financial management skills
  • Excellent time management and organization skills
  • Ability to effectively prioritise your own workload
  • Self-sufficient and capable of working within an environment where deadlines are critical
  • Energetic personality with strong personal presence and lots of enthusiasm

You must have the right to work in the UK at the time of being offered employment.

Company benefits

In return you will receive a competitive salary, a generous benefits package, excellent training and development, as well as an exciting career within a fast paced and dynamic business.

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