What do we do? Phlexglobal is your complete solution for resourcing needs, whether you are looking for a new role or need someone to join your team. We are a specialist CRO who have been delivering clinical study support solutions for more than 10 years. Our unique blend of core services together with our industry knowledge and expertise means we are ideally placed to help you with any resourcing needs you may have.
We are exceptional in the market place and in this time of financial uncertainty we are breaking the trend and expanding our core teams.
Phlexglobal's Task Force is a unique approach within the industry; they are the industry's 'hit-squad', supporting all aspects of clinical research, working with large and small pharmaceutical companies to NHS Trusts. Projects are short term focused, assisting our clients with resource shortfalls.
Our Task Force is growing rapidly and we are looking for a number of talented individuals to join the Task Force team. Are you motivated, flexible, highly organised and a team player looking for a new challenge? You will be an Ambassador of Phlexglobal and will work with the Task Force team to drive and develop the Task Force.
• Clinical Project Associates (CPA) - Recent life science graduates who are looking to start their career within clinical trial administration. Full training and support is provided.
• Clinical Trial Administrators – We are looking for both Career CTAs and CTAs looking to become CRAs. We are able to offer you the training and support required, through our Training and Personal Development department, in order to progress your career either as a CTA or there is the potential to join our Development CRA programme.
• Study Support Specialists (Senior CTAs) - We are always looking for career CTAs and offer continued personal and career development, such as exposure to coaching and mentoring, project co-ordination and training.
• Clinical Research Associates - Work within the Task Force providing monitoring support to client’s across the UK within the non-commercial and commercial trial arena.
We have extensive experience in the management of Trial Master File (TMF) documentation and are leading the field in electronic TMF management. As a result we are building our eTMF and Document Solutions team and looking for the following to join the team:
• Document Administrators - Providing logistical support to in-house eTMF and document solution projects.
• Document Managers – To provide both quality and logistical support to in-house projects including document preparation. This role will include client liaison and query resolution.
• Team Leaders - Ensuring all client projects are consistently delivered to the highest level within budget and to agreed targets. Manage a team at the front end of the eTMF process and provide training and knowledge of clinical study processes and documentation.
Phlexglobal offers a flexible and adaptive support solution to managing clinical studies for both the commercial and non-commercial sectors, in Europe and the US. If you would like to find out more about our services, please contact Toni Lakin on 01494 720287 or if you would like to join our team please contact the Resourcing Department on 01494 720439.
What do our employees think?
"I enjoy working within the Task Force for the huge variety of work that we undertake. There is no time to get bored or stale as you are constantly moving from one project to another." – Study Support Specialist
"The Task Force is a unique department that allows a graduate fresh in the industry to gain exposure within the commercial and non-commercial environments. The potential to work in different phases or a clinical trial coupled with the ability to make a considerable network of contacts is the most rewarding prospect for working within Task Force." – Clinical Project Associate
"Working in the Task Force has been thoroughly enjoyable as it offers such a diverse range of work within clinical research. The exposure to different clients meant that you are able to acquire proficient skills in such a short amount of time as well as meet wonderful people along the way." – Development Clinical Research Associate
"The opportunity to work at the cutting edge of clinical document management with regards to systems and process is really exciting and rewarding." – Document Administrator
"Having worked as a CTA, working for an organisation that really understands the value and importance of the TMF to its clients is a great place to be. I have been given the opportunity to show and deliver my managerial and leadership skills." – Team Leader