James Hume is seeking a Project Manager to join a clinical stage T cell therapy company in a strategic role with responsibility for the management of R&D programmes from development to commercialisation. They are continuing to expand as they have a number of products they are developing and then transfer to the clinic, manufacture and commercialise. With some already in the clinic they have others at the earlier stages of R&D that they are seeking to take to the clinic as well as other concepts behind this. The Project Manager is a strategic role where you will be coordinating all the different aspects to bring therapies to the clinic and ultimately launch.
A pioneering and ambitious Biopharmaceutical company who develop next-generation, programmed T-cell therapies to treat haematological cancers and solid tumours. The organisation has existed for 4 years and is very well funded, with a clear strategy and expansion plan for the next 3 years and beyond. Scientifically, the company has extremely exciting technologies, using a broad suite of proprietary and modular T-cell programming to engineer precisely targeted, controlled and highly active T cells. Commercially, they have a pipeline of product candidates in development (for the treatment of haematological malignancies and solid tumours) and is increasing its GMP production capacity. Based in a state-of-the-art facility in Stevenage, Hertfordshire, you will join a team that is doing something genuinely meaningful.
The role of Project Manager is to be responsible for a number of projects, taking them through the latter stages of R&D, to the clinic, through trials to commercial launch. Meeting the compressed timelines they have by coordinating across different departments and activities where detailed planning is crucial to success in this critical role.
You will be working cross functionally within the Product Delivery team and others such as regulatory for example. The Product Delivery team are responsible for the development of CAR – T manufacturing processes, their manufacture for clinical trials and setting up commercial manufacture in the future. You will ensuring each step of the process is achieved and progressing as schedule. With involvement in decision making and playing a key role in the identification of bottlenecks, conflicts and scenario planning and how to resolve these. This role also includes activities related to CMC input into development programmes and other programme such as new technology introduction or new facility set up.
This is a higher-level role where you will be visible with excellent long-term career progression opportunities. As well as having a direct impact on the progression of life changing therapeutics through the commercialisation process to become available to patients with critical illnesses.
Desired Skills and Competencies:
For this role, you will need to have demonstrable experience of project management with CMC experience in a similar environment e.g. T Cells and Viral Vectors. For example, gaining experience in any of the following sectors: biotech / biopharma / CMO / CRO / clinical trial / clinical supply chain sectors. You will be educated to a level higher than degree or equivalent in a relevant scientific field. With the ability to work with multi-disciplinary teams as well as external clients to plan, manage and deliver R&D projects.
Salary and Benefits:
- Salary – Competitive
- 25 Days Holiday
- Pension – 5% matched contributions
- Life Assurance – 4 times base salary
- Group Income Protection
- Private Medical Insurance
- Dental Cover