Job Title

CTA / Study Coordinator, Oxfordshire

Salary

<£30,000

Job Type

Clinical Study Administration

Location

Oxfordshire

Employment Type

Permanent Job

Employer Type

PM Biotech

Seniority

Assistant/Associate

Duration

 

FTE Hours

Full Time 35 - 40hrs Per Wk

Vacancy Status

Open For Applications

Date Posted

Thu 9th Oct 2008, 01:35pm

Our client is a leader in the discovery and development of novel small molecule drugs. The Company has established a powerful platform that is applicable to targets across all therapeutic areas and has specific expertise in the area of Central Nervous System (CNS) related diseases. They are currently looking for a super CTA to join them on a temp to perm basis in Oxfordshire, offering excellent benefits!

The purpose of the role is to organise, maintain and manage filing systems for clinicaltrial documentation.
Provide administrative and logistical support.
Maintain systems for the control, tracking and storage of documents for the Clinical Development Department including both electronic and hard copy documents, operating in accordance with SOPs and GCP.
Liaise with Project Teams to set up and maintain Trial Master Files/ Study Files including checking that trial documentation before, during and after trial completion are in accordance with SOPs and GCP.
Act as the named Archivist for Clinical Development documentation.
Organise quarterly Clinical Development Department Meetings including organisation/ preparation of agendas and minutes of meetings.
Super CTA also manages SOP control, trackers and budgets
Act as the named Archivist for Clinical Development documentation.
Organise quarterly Clinical Development Department Meetings including organisation/ preparation of agendas and minutes of meetings.
Assist in monitoring/management of clinical sites, as required.

Qualifications and skills required:

Good communication skills, Good pc skills - Microsoft Excel, Microsoft Powerpoint, Microsoft Word. Also required are excellent organisational skills and an ability to deal with and track numerous documents^operating in accordance with SOPs and GCP