Job Details 
Phlexglobal
Our database has identified the following jobs as matching your search criteria. If you cannot see a job you are interested in, please search again refining your criteria or email us for further help and support.| Title | Project Support Specialist | ||
|---|---|---|---|
| Role | Clinical Trial Administrator | Reference | CH10669 |
| Location | Buckinghamshire | Working hours | Full-time |
| Salary | On application | Employment type | Contract / Interim |
| Summary | Are you an experienced Clinical Trial Administrator? Our Clinical Support Services Group offer complete or partial project outsourcing, working with the Phlexglobal Task Force and other external vendors. You will be flexible, with the ability to provide full clinical and logistical project support to client companies. You will gain a huge range of exposure through working with pharmaceutical, CRO, biotech clients and the NHS. | ||
| Description | As a PSS you will need to be an organised, logical, enthusiastic and methodical worker with proven ability to coach, mentor, listen and inspire others. You will ensure that all client projects are consistently delivered to the highest level within budget to agreed targets. Lead a team allocated to specific projects, ensuring compliance to applicable global regulation and company policies and procedures. Provide training and knowledge of clinical study processes and documentation. Carry out document processing and Quality Control checks (QC). Responsibilities include: • Leading a team responsible for the quality control of several aspects of eTMF workflow including performing quality checks on work completed by other Project Team Members. • Become a Super-user within a Client Project team, to be experienced and practised in all elements of delegated projects. • Work with Project Manager(s) to define process/workflow procedures and exception handling per project. • Perform Quality Control (QC) of trial documents filed in a clients eTMF or Phlexglobal’s eTMF (PhlexEview) in accordance with Phlexglobal or the client company SOPs. • Work with Project Manager(s) to analyse project data and various matrices to ensure quality-related productivity remains high, error rates are low and targets are achieved. • To provide daily, weekly and/or monthly reports to Project Manager(s) and/or Senior Operations Manager. • Trouble shooting, resolving equipment problems/failures and rectifying processing issues immediately for delegated Project Team. • Responsibility for ensuring compliance with client and Phlexglobal SOPs (Standard Operating Procedures). • To work with the Senior Operations Manager and Project Managers to review processes and recommend efficiency changes to existing processes. • Provide support to other CSS staff as required. Candidates must live within a commutable distance from our offices in Amersham, Buckinghamshire and be eligible to work in the UK. Phlexglobal is a leading quality driven Contract Research Organisation who only select the best. Ours is a people culture and we are committed to nurturing and training self-motivated, exceptional Clinical Research Professionals. | ||
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