FAQ

Not sure what type of company Phlexglobal is or what services we offer?

The following questions should help answer these questions. However, if you can't find what you are looking for, please contact us for further information.

 

Q - Do Phlexglobal manage full-service clinical trials?

A - Yes, through our in-house expertise and qualified external vendors.

 

Q -  Do Phlexglobal only recruit for Clinical Trial Administration roles?

A - No, we have a broad range of roles working with a variety of clients from large and small scale pharmaceutical and medical device companies, biotechnology organisations, the healthcare sector and other CRO's, both in the UK and abroad. Phlexglobal is delighted to be a preferred supplier to many companies running clinical trials and have roles ranging from CTA, CRA, Project Manager, Data Manager, Regulatory Affairs Specialist, SAS Programmers and more. Our vacancies change daily, search for current vacancies or contact our resourcing team for further help and advice on +44 (0) 1494 720439.

 

Q - I have an inspection / audit coming up shortly and need some help getting ready for it, can you help?

A - Yes, the Phlexglobal Task Force is ideally placed to respond to short term projects such as audit and inspection readiness. In addition, our training department have courses that deal with preparing for inspection which can be tailored for specific client needs.

 

Q - I am considering moving my paper based Trial Master File (TMF) onto an electronic system but I don't know where to start.

A - Phlexglobal is at the forefront in the move from paper to electronic TMF management and storage. We have trained, experienced document administrators, document managers, scanning operatives, project managers and IT change management consultants to facilitate the process. We can provide trained and experienced resource to perform the necessary migration and ongoing support either based at our offices in the UK; or we can work from a client's site.

 

Q - Can Phlexglobal support other TMF systems or do you only support your own system?

A - Phlexglobal's eTMF and Document Solutions team are experienced in using a range of systems, working through remote access to client systems.

 

Q - I am looking for some advice on how I can gain efficiencies in running clinical trials using outsourcing or other flexible resourcing models. Can Phlexglobal help?

A - Yes, we can provide advice and consultancy services to clients looking to use a variety of resourcing or service provision models to gain efficiencies in running their clinical trials.