Clinical Trial Administrator

Recruiter
Hays Specialist Recruitment Limited
Location
Uxbridge
Posted
12 Apr 2018
Closes
20 Apr 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
An experienced Clinical Trial Administrator

Your new company
An independent biopharmaceutical company pioneering immunotherapy treatments, in particular for cancer.

Your new role

To ensure that trial master files are organised, maintained and complete, clinical operations project managers are supported on day-to-day study management activities and clinical operations functions are supported in order to assist in the delivery of Clinical Development objectives and achieve clinical excellence.

* Organise, maintain and complete the paper and electronic trial master files, including collation of study documents from monitors or CROs and appropriate filing of documents.
* Identify, request and ensure delivery of outstanding and outdated documents.
* Periodically, and at the end of the study, review study files / folders for organization and completeness.
* Assist in setting up clinical study files / folders at study sites and assist in quality review of the study site files / folders throughout the study.
* Conduct in-house clinical operations functions, including clinical supplies coordination, , Assist the COPM in investigator meeting preparation and coordination, document processing and study status tracking.
* Arranging and minuting Study Team Meetings (as required) and completing actions as necessary.
* Assist in the project management and monitoring of clinical studies, including liaison with study sites, monitors, CROs, drug vendors, central laboratories and other vendors for study related tasks.

What you'll need to succeed

* Substantial administrative experience or qualified to degree level. Scientific background is essential.
* Experience or knowledge of regulatory documents or medical terminology.
* Experience in clinical operations area related work.
* Working knowledge of computer applications including Microsoft project.
* Able to produce work of high quality in a timely manner.
* Up-to-date GCP training.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
This job was originally posted as www.emedcareers.com/job/960519137

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