Our Regulatory Affairs team holds extensive industry experience shaping project plans to meet diverse regulatory requirements
Job Summary
Our Regulatory Affairs team holds extensive industry experience shaping project plans to meet diverse regulatory requirements.
Liaise with SAR colleagues to drive plan, organize, compile, progress, track, and submit regulatory submissions on a timely basis and with a consistently high level of quality.
We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.
Matching Summary
Our Regulatory Affairs team holds extensive industry experience shaping project plans to meet diverse regulatory requirements.
Skills & Requirements
Must-have
Regulatory submissions
ICH GCP compliance
Country-specific requirements
Clinical research experience
MS Office proficiency
Nice-to-have
Multilingualism preferred
Cultural norms understanding
Relationship development
Key Requirements
Minimum four-year college degree
Minimum three years clinical research experience
Experience in regulatory submissions in Australia and Singapore preferred
Thorough knowledge of ICH GCP and EU Clinical Trials Directive