Senior Clinical Research Associate, home or office based

Munich, Bavaria, Germany

Description

The Senior Clinical Research Associate (SrCRA) is part of Clinical Monitoring within TFS Develop and will function operationally as a member of a Project Team and is responsible for the initiation, on-site and remote monitoring and termination of investigative sites during study conduct, according to company policies, SOPs and regulatory requirements.

The Sr CRA may assist the Project Manager in certain aspects of project activities which may include project tracking, monitoring plans, review of monitoring reports and CRA resources management.

The Sr CRA may also conduct all stages of site monitoring (feasibility, pre-study, initiation, interim, and close-out). Ability to travel as needed; may involve overnight and international travel.


Essential job functions:

Requirements

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