Company Overview: Quotient Clinical
Our growing and successful business comprises over 350 talented individuals in an environment where everybody counts and is instrumental to our success.
People join Quotient Clinical 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. 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.
Learning and development is at the heart of our culture at Quotient and you will be given every opportunity to reach your potential with us. You’ll be recognised for your contribution and rewarded with genuine career development, a competitive salary & a whole host of benefits.
Due to our continued growth and success we have an excellent opportunity for a driven individual to join our Project Management team. This role will be responsible for our Pharmaceutical Development and Supply service line.
This on demand flexible manufacture capability sets us apart from our competitors and enables us to supply drug products to other clinical centres of excellence worldwide. This is an area of significant opportunity and we have already celebrated a number of successes working within paediatrics and oncology for patient/POC studies.
In this role you will be responsible for the day-to-day management and completion of allocated projects. In this role you will be expected to deliver service excellence for our customers across the globe and over a range of therapeutic areas. You will develop a project plan and lead a multifunctional project team to deliver that plan to time, cost and quality.
You will be responsible for generation and/or review of key study documentation and will lead external and internal communications to ensure adherence to the project plan and ensure the project team has a depth of understanding of customer requirements. You will be responsible for ensuring any third party contracts needed to support are in place and ensuring appropriate oversight processes are adhered to.
You will also be required to support account management working with commercial colleagues to develop proposals that support our customers with the development of their drug development programmes.
To succeed in this fast-paced, delivery-driven environment you will need to be qualified to at least degree level in a life science subject, and have a minimum of 2 years’ pharmaceutical sciences experience with a good understanding of the drug development process and cGMP procedures. Phase 1 experience and working in the service sector would be advantageous but not essential.
You will need excellent project management, customer service and financial management skills, as delivery will be your main focus. You will need to demonstrate excellent time management skills, be organised and be effective at prioritising workloads.
In this role you will be working with multifunctional teams and therefore you will be required to work and communicate effectively across different areas of the business. Being able to build strong working relationships and to collaborate and influence colleagues and stakeholders is key.
You will need to be self-sufficient and capable of working within an environment where deadlines are critical. You will have an energetic personality with strong personal presence and lots of enthusiasm.
Applicants must have the right to work in the UK upon being offered employment.
As well as offering ongoing training, we offer flexible working, private healthcare and life assurance, 33 days holiday (inclusive of bank holidays) & group pension plan.
We have various recognition and appreciation schemes in place to say ‘Thank you’ to our staff for all their hard work e.g. employee of the quarter, food treats and staff parties. We provide a subsidised restaurant and have free parking at our site in our leafy surroundings just outside Nottingham.