Phlexglobal supports clients where enhanced IT systems and processes often require more focused specialist support and expertise to ensure accuracy, integrity and quality of collected data. Our trained and qualified professionals can perform individual or groups of tasks. We support research departments and other groups, such as marketing, based either at Phlexglobal (using remote working methods) or from the clients’ own offices.

We offer clients ongoing and long term project support with central project management and line management from Phlexglobal. Our experienced Clinical Trial Administrators can support activities related to study documentation; Investigational Medicinal Products and study supplies tracking; clinical trial management systems and tracking tools; electronic Case Report Forms (eCRF).

Clinical Support Services can also offer complete or partial project outsourcing developed around a ‘pick list' system, working with the Phlexglobal Task Force and other external vendors.

• Clinical Trial Administration and Specialist Support
• Project Management
• Project Outsourcing

Monitoring Services

Meeting the challenge of continually changing regulations, we support clients in efficient monitoring of clinical studies from Phase I to Phase IV and across a range of therapeutic areas on an interim or long term basis. We have established a ‘pool of excellence’ with trained and experienced Clinical Research Associates (CRAs) who can conduct, record and report clinical studies in accordance with the protocol, relevant Standard Operating Procedures and applicable regulatory requirements.

Phlexglobal offers a flexible solution enabling clients to choose from a full monitoring service or selection of one or several areas for support. Our CRAs are experienced in a range of site management activities including: study feasibility, site selection, Ethics Committee applications, site initiation, monitoring and study close-down.