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Sr. Clinical Project Administrator (22104BR)


Save this Job ID: 298142
Company Name: View All Covance Jobs Approximate Salary: Not Specified  
Location: , Any Country: Germany
Industry: Clinical Research Position type:Full Time
Experience level: Typically required : Preferably two (2) years administrative experience in a corporate environment or, minimum of one (1) year Clinical Project Administrator experience Good oral and written communication skills Ability to set priorities and handle multip Education level: Typically required: Diploma Secondary Education or equivalent Thorough knowledge of the contents of investigator documents and the applicable regulations and Covance Standard Operating Procedures for their use.
Clinical Research
Covance is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries.Due to our continuous growth, we are looking for an enthusiastic and experienced Senior Clinical Project Administrator office-based in Munich Duties and Responsibilities:
The handling of multiple sites and a close co-operation with inhouse and external CRAs as well as the project manager
Provide clerical support for clinical projects to project team (e.g. word processing, proofreading and editing correspondence, mailings, shipment of study files, fax and photocopy documents, assemble study documents, and arrange meetings, etc.)
Completion and control of tracking sheets
Set up and maintain clinical investigator files and documentation
Prepare study-related documents and other materials for delivery to archives
Prepare investigator budget payments and tracking systems; generate tracking reports, SUSAR reporting to sites and ethic committees
Data entry and maintenance of selected study tracking data
Assist/prepare for client or internal audits
Provide telephone coverage and related support duties

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