Base: $170,000 to $187,000; bonus/equity: eligible...
Onsite (summit, nj)
Clinical regulatory strategy development
Regulatory submissions in ectd format
Strong knowledge of health authority guidance
ImmunityBio, Inc. is seeking a Principal Specialist for Health Authorities to contribute to the development of global clinical regulatory strategies and manage regulatory submissions. The role requires extensive experience in clinical data evaluation and regulatory documentation in a biotechnology setting
Job Summary
ImmunityBio is developing cutting-edge technology to transform the lives of patients with cancer.
The Principal Specialist will assist in the preparation and review of regulatory submission packages.
Employees are offered a competitive benefits package and opportunities for professional development.
Matching Summary
Match Score: 85
ImmunityBio, Inc. is seeking a Principal Specialist for Health Authorities to contribute to the development of global clinical regulatory strategies and manage regulatory submissions. The role requires extensive experience in clinical data evaluation and regulatory documentation in a biotechnology setting.
Salary
Base: $170,000 to $187,000; Bonus/Equity: Eligible; Benefits: Comprehensive benefits package
Skills & Requirements
Must-have
Clinical regulatory strategy development
Regulatory submissions in eCTD format
Strong knowledge of Health Authority guidance
Nice-to-have
Experience with international regulatory submissions
Ability to manage multiple deadlines
Strong organizational and communication skills
Key Requirements
Bachelor’s degree in life sciences or technical discipline
10+ years of relevant experience
Expert knowledge of clinical research and regulatory guidelines