Spécialiste Soumissions Règlementaires - Sponsor Dédié - Home Based Canada
Syneos Health
Canada
Remote
Clinical trial submission management
Regulatory authority liaison
Quality control of submission documents
Join a company that is reinventing how therapies are developed and marketed, bringing biopharmaceutical therapies to patients faster
Job Summary
Join a company that is reinventing how therapies are developed and marketed, bringing biopharmaceutical therapies to patients faster.
You will be responsible for preparing, submitting, and tracking clinical trial applications with competent authorities and ensuring quality control of documents submitted to ethics committees.
Syneos Health is committed to developing its people through career progression, training, and a supportive 'Total Self' culture where diversity is celebrated.
Matching Summary
Join a company that is reinventing how therapies are developed and marketed, bringing biopharmaceutical therapies to patients faster.
Skills & Requirements
Must-have
Clinical trial submission management
Regulatory authority liaison
Quality control of submission documents
Clinical research experience
Nice-to-have
Agile and driven team
Passionate problem solvers
Collaborative environment
Focus on patient well-being
Key Requirements
Experience in clinical research within a CRO or pharmaceutical company
Experience managing regulatory submissions to ethics authorities