Job Details
Job Reference
J661451
Company
Job Title
Senior Clinical Research Associate
Contract Type
Contract
Sector
Country
Town / City
South, South East
Salary
Description
Senior Clinical Research Associate
Our client is one of the largest and most widely respected pharmaceutical companies in the world. With a very strong product portfolio and successfully enhancing the quality of life of millions, you would not want to miss an opportunity to work for them! They are now looking for an experienced Clinical Research Associate to work fully field-based in the South East area. The position is a 12 month rolling contract, where you would be a permanent employee of Clinical Professionals and receive our very competitive benefits package! This is a fantastic opportunity for current CRA/SCRAs to gain further responsibilities such as budget management.
Major Accountabilities of the role are to:
-Participate in site nomination process; perform evaluation of site capability and make recommendation for inclusion in clinical trial.
-Assume ambassadorial role to facilitate communication between sites and Key companies line functions to increase value proposition to investigators.
-Facilitate preparation and collection of site level documents.
-Execute site initiation and training activities.
-Perform monitoring visits according to monitoring plan.
Main requirements for the role are:
A degree in a scientific or healthcare discipline preferred
Basic medical and business knowledge
Understands and can apply knowledge of clinical trial designs to trial execution
knowledge and experience in international standards, international and local regulations
Expertise in communication, managing multiple priorities and computer literacy.
Keywords: CRA Clinical Research Associate Clinical Research Scientist Field-based Contract senior clinical research associate SCRA CRA JPM uk wide south south eastPosted
2009-01-09 10:20:04 +0000
Ideal Candidate
Main requirements for the role are:
A degree in a scientific or healthcare discipline preferred
Basic medical and business knowledge
Understands and can apply knowledge of clinical trial designs to trial execution
knowledge and experience in international standards, international and local regulations
Expertise in communication, managing multiple priorities and computer literacy.
An EU passport or work permit is required for this position. Applicants without one of these will be rejected automatically.


