Study Start- up Specialist (Temporary)

Roche A.Ş.

• University degree or equivalent in a medical/science-related field
• Advanced level of English in written and spoken English
• Project Management experience
• Excellent communication skills
• Excellent planning & organization skills
• Multi-tasking
• Problem Solver
• Team Player
• Knowledge of MS Office software, web-based systems and databases
• Ability to travel domestically and internationally if required

The candidates with the following qualifications will be prioritized:

• Prior work experience demonstrating knowledge and understanding of clinical trials and project management
• Good knowledge of ICH-GCP, the regulatory, ethics and contractual requirements for starting clinical trials

İŞ TANIMI

The function of the Study Start-up is to start the clinical studies compliant with the timelines
and in compliance with all quality process and the legislation. To achieve these functions,
communication with all related internal and external stakeholders is necessary. To maintain
the compliance at the start up and during the conduct of clinical studies, Ministery of Health
and Ethic Committee submissions must be performed in a quality oriented and timely manner as per the job description.