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Fforde Management
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Clinical Project Assistant - 12 Months Contract



Business Type: Clinical Research Organisation
Job Type: Clinical Research, Clinical Study- Trials, Project Management
Job Level: Not Specified
Position: Contract
Salary: Competitive & Benefits
Location: UK - South East
Reference: 17677/001
Closing Date: 17/05/12
Background:
Our client, a specialist global pharmaceutical company and innovative leader in pharmaceutical and health care research and development, is mainly concerned with development activities. They are seeking a Clinical Project Assistant for a 12 month contract at their Buckinghamshire location.

JOB ROLE:
The Clinical Project Assistant will provide administrative assistance in documentation preparation, tracking, and filing of key information for the conduct of clinical research studies/projects.

PRINCIPAL RESPONSIBILITIES include:
Ensuring tasks associated with the set up, implementation, and completion of all studies in accordance with appropriate Pharmaceutical Legislation and Directives, including confirming that all materials have been received by the site and all documents have been appropriately archived
Assist in the creation and distribution of Site Feasibility Surveys
Update Study Timelines In Electronic Clinical Trial Tool (e.g. CTMS)
Assist with drafting a Site List by compiling a preliminary Site List and entering it into CTMS along with site metrics from previous studies etc
Assist in generation, compilation and distribution of essential regulatory documents
Coordinates the critical documentation process and tracks information received in-house
Assist in Preparation for Site Initiation by sending materials to site
Compiles and distributes all site initiation packages
Assist in the Processing of the Initial Drug Approval Package
Maintains patient recruitment logs across sites to ensure timely drug supplies at sites; distributes patient enrollment logs as defined in the monitoring plan; ensures patient enrollment graphs are current.
Assist with archival and storage of TMF Documents including assisting with a quarterly review; files documentation of clinical study related communication in TMF

QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
Strong experience from a similar background as CTA, CPA, from either a Pharma or CRO
Has worked across multiple studies
European experience would be preferred
Strong word and excel skills
Ability to multi task and priorities
Strong attention to details
Strong communication skills

PERSONAL SKILLS & ATTRIBUTES:
Strong word and excel skills
Ability to multi task and priorities
Strong attention to details
Strong communication skills


BENEFITS OF THE ROLE: This leading pharmaceutical company is committed to fostering a friendly work place with no discrimination. They offer competitive annual salaries together with excellent benefits that include Pension Plan, Life Assurance, Private Medical Insurance, Disability & Accident Insurance, good Annual Leave, Performance related Bonus, Free Car Parking, Subsidised Restaurant, Sports & Social and more.

Fforde is acting as a recruitment agency/business.

KEY WORDS: Clinical Research, Clinical Project, Project Management, Administration, Administrative, Clinical Studies, Clinical Trial, Pharmaceutical, CRO, Buckinghamshire, UK

Posted: 10/05/2012 | NPJ Ref: 81840
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