The Phlexglobal Task Force is a team of trained and experienced industry professionals who are available to provide interim and short term project based support to clients across the industry both commercially and non-commercially within the UK and Europe.

Phlexglobal’s Task Force offers an independent and flexible approach to ensuring projects are appropriately resourced and managed whether on a global or local level. We respond to immediate interim needs for experienced clinical research professionals. Clients can call on the services of our trained clinical professionals to support projects at any stage, working either at the client offices or based at the Phlexglobal office. 

The team has a wealth of experience within clinical research gained from working on a range of commercial projects within large and small pharmaceutical, medical device, CRO and biotechnology companies. We have successfully supported a number of non-commercial projects working with investigator sites, Research and Development departments and within Research Governance.

Supported by their Freelance Register, the Task Force have additional flexibility for resourcing projects, ensuring that all projects are allocated to appropriately trained and experienced staff to ensure project deliverables are met. If you are interested in joining the Freelance Register, please click here.

Phlexglobal's Task Force model is a unique approach within the industry, providing interim and flexible support services to clients. Working closely with clients to understand their specific business needs, the Task Force will assign appropriate individuals to complete the project from three core service teams:

-    Clinical Project Associates (Task Force 1). General project administration tasks, such as TMF set-up, quality checks, collation, tracking and archiving of essential study documentation.

-    Clinical Trial Administrators (Task Force 2). Experienced CTA support to 'hit the ground running' for traditional CTA activities or to focus on specialist areas such as TMF review, study start-up or close-down activities and Research Governance.

-    Specialist support (Task Force 3). Support in the development and implementation of SOPs, working practices, quality assurance activities, project and line management activities. Providing specialist resource from our internal staff or through our Freelance Register of experienced Project Managers, Auditors and other clinical research professionals.

All of the Task Force staff are CRB cleared (UK) and are fully trained in clinical research guidelines including GCP and the EU Directives.

Project support can be provided to clients from as little as one day up to six months. Depending on individual project and client needs, this support can be delivered at client premises; in-house at Phlexglobal's offices in Buckinghamshire, UK; or by flexible home-working. Phlexglobal have operational workstations manned by experienced Task Force personnel and these are capable of interfacing with client servers through secure connections. 

Phlexglobal's Task Force offers clients an independent, impartial, quality service that is both process driven and works in collaboration with the client at all times.