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Section:  Other   Vacancy 1197

Post:CLINICAL TRIALS ASSISTANT Salary contractual
Requirements and conditions
Age: Has no value
Gender Has no value
Education: no
Work schedule: Has no value
Work place: London
The announcement text:
Support members of the study team to implement and manage study activities from initiation to close-out.



PRIMARY JOB RESPONSIBILITIES:



1. Collect and review study related regulatory and financial documents. Distribute copies to appropriate departments.

2. Organize and maintain project working files and track critical documents.

Submit documents to IRB



3. Track and process site and vendor payments.

4. Collect trial enrollment information and update study management reports under the guidance of the Clinical Scientist (CS)/Clinical Trial Manager (CTM).



5. Support and correspond with investigative sites as necessary, including ordering study drug and other trial related supplies.



6. Assist with the preparation of clinical team meeting agendas and minutes, and monthly site newsletters.

7. Communicate and support field monitors, IRBs and outside vendors as to study issues and updates.

8. Participate in the planning, preparation and on-site support of investigator?s meetings. Will occasionally make brief presentations at an investigator?s meeting.

ADDITIONAL JOB RESPONSIBILITIES:



1. Attend clinical team meetings.

2. Contribute to process improvement efforts including task forces and committees

POSITION QUALIFICATIONS:



EXPERIENCE A MUST NO EXCEPTIONS.



SEND RESUMES TO CPROUDLOCK@EDCPHARMA.COM









Compensation: TBD

Principals only. Recruiters, please don`t contact this job poster.

Please, no phone calls about this job!

Please do not contact job poster about other services, products or commercial interests.



Contact information
Employer: Виктория
Email: CPROUDLOCK@EDCPHARMA.COM
Phone: тел. 5021138, 8066-852-87-40
Publication date: 2009-09-26 12:25:37

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