Key Responsibilities:
* Lead the team responsible for initial Intake of adverse event data and subsequent reporting of Individual Case Safety Reports to health authorities, partners and internal destinations in compliance with global regulations.
* Develop and implement processes and systems to enable timely reporting and accurate safety information sharing.
Skill Requirements:
* Proven expertise in clinical research process and global pharmacovigilance regulations, systems and processes.
* Strong knowledge of advanced data validation and analytics tools.
* Effective leadership and people management skills.
The ideal candidate should have a Bachelor's Degree in one of the life sciences or clinical research, as well as 12 years of experience in safety and safety reporting.
Key Qualifications:
* Certified healthcare professional required.