Bachelor's degree required, preferably within Life Sciences or equivalent

• 3+ years of industry related experience, including handling of trial start-up activities coordination of trial start-up activities and Health Authority / Ethic Committee submissions and contract negotiation

Must Have
• Minimum qualifications posted above;
• Thorough understanding of GCP, ICH Guidelines and Country regulatory environment;
• In depth knowledge and understanding of clinical research processes, regulations and methodology;
• Demonstrated organizational and planning skills and independent decision-making ability;
• Experience in leading or participating as an active member of cross functional teams, task forces, or local and global initiatives;
• Strong organization and time management skills and ability to effectively manage multiple competing priorities;
• Ability of critical thinking and risk analysis.

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