Job Title

Experienced CTA wanted, Warrington, NW

Salary

<£30,000

Job Type

Clinical Study Administration

Location

Cheshire

Employment Type

Permanent Job

Employer Type

PM Pharmaceutical R&D HQ (Global Or EU)

Seniority

Assistant/Associate

Duration

 

FTE Hours

Full Time 35 - 40hrs Per Wk

Vacancy Status

Open For Applications

Date Posted

Thu 17th July 2008, 05:23pm

CTA role in new exciting and growing healthcare company based in the North West!

Introduction

Our client is seeking an experienced Clinical Trial Administrator to join their company in the North West. Previous CTA experience is essential as this is a small team, and the CTA is a key member of the team. Our client are a rapidly expanding company with a commitment to providing novel drugs into the Renal Disease and GI Disease areas.

Summary of duties
To provide comprehensive supportto the clinical team forthe set up and administration of clinical trials ensuring adherence to protocols and quality of information received, in line with UK & EU regulations, GCP guidelines and company SOPs
Facilitating submissions of NHS R&D/PCT and ethics committee applications ( e.g. copying and filing regulatory documents and providing administrative support)
The efficient and accurate administrative processing of forms concerning data collection, paymentsand other materials with regard to^clinical trials. Activities are based on the guidelines as described in company SOPs
Set up and maintenance of the trial documentation files, study records and tracking systems including electronic documents in accordance with ICH GCP and the company SOPs in such a way that any relevant information can be presented promptly during internal or external audits.
Be an internal focal point for Clinical Team, ensuring appropriate dissemination of information to team members

Qualifications needed
Previous CTA experience or similar administrative experience
Good Word, Excel and internet skills
Well organised with the ability to multi-task
Some knowledge of ICH-GCP preferred