Ref #: 21588

Employment type: Permanent - Full-Time

Location: Buckinghamshire

Posted: 13-Nov-2020

Description

Key CTS Responsibilities include:
• Supporting the management and oversight of global clinical trials
• Essential document management
• Maintaining study level storyboard for critical timeline oversight
• Compiling IRB/EC submission documentation
• To coordinate, author and manage preparation of clinical trial documentation and training materials (including investigator meetings, site evaluation and initiation training)
• Facilitate development of Investigational Product Information Manual and study specific Important Protocol Deviation list
• Managing processes for planning, procuring and oversight of ancillary clinical supplies
• Creation and management of study specific tools, including:
o Global/country level recruitment and retention materials
o Authoring and distribution of study newsletters
• Vendor management (including set up, tracking and issue resolution over the life of the study)
• Tracking and collation of study data and metrics utilizing multiple clinical systems
• Preparing clinical study team meeting agendas and minutes, facilitating cross-functional meetings
• Managing global versioning and distribution of documents (e.g. informed consent forms)

What is offered
• Permanent full time contract of employment with DOCS seconded to the client
• Structured 4-week on-boarding
• Office-based in Marlow (Bucks) or in Eastleigh near Southampton (Hampshire) with the flexibility of up to 2 days’ home-working per week.
• Salary depending on level of skills and experience plus company benefits (23 days’ annual leave, pension, healthcare cover, etc.)

For more information and full job details, please contact me with your CV today to Elisabeth.Knighton@docsglobal.com or ring +33 964 25 67 65.

*Applicants who have not had a response within two weeks should assume their application has been unsuccessful.