- Gaithersburg, Maryland, United States
- Hybrid
- Full-time · Director
- $132K–$199K per year
1–10 jobs· newest first
$132K–$199KHybrid · Full-time · Director

$132K–$199KHybrid · Full-time · Manager
$132K–$199KFull-time · Manager
$203K–$305KFull-time · Director
Manager
$205K–$342KHybrid · Full-time · Director


Full-time · Senior
+10K new in the last hour
The role leads defined safety science activities for assigned cell therapy assets, integrating safety data, supporting benefit-risk decisions, and managing patient risks across the product lifecycle.
The annual base pay for this position ranges from $132K to $199K. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.
Lead safety science activities for cell therapy assets within the Global Patient Safety Unit, integrating data, managing risk, and supporting regulatory submissions.
The annual base pay for this position ranges from $132K to $199K. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.
Lead safety science activities for cell therapy assets within the Global Patient Safety Unit, integrating data, managing risks, and supporting regulatory submissions.
The annual base pay for this position ranges from $132K to $199K. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.
A senior scientific leader within the Cell Therapy Patient Safety Unit leading safety science strategy and delivery for complex cell therapy assets, integrating clinical, nonclinical, epidemiologic, and real-world evidence to shape safety profiles.
The annual base pay for this position ranges from $203K to $305K.
Lead the drug safety and pharmacovigilance function in Japan, ensuring compliance with local regulations and driving safety processes.
The Director serves as the first point of contact for all Rare Disease operations including safety data processing, submission creation, and documentation to ensure completeness, accuracy, and timeliness.
$205,000.00 - $341,600.00
Lead review of safety data and related documents for potential safety issues in collaboration with Global Safety Physician and PV Scientist, author and lead PV input to safety documents and regulatory reports.
Lead review of safety data and related documents for potential safety issues in collaboration with Global Safety Physician and PV scientists.
A broad role that combines strategic oversight with hands-on pharmacovigilance operations, offering exposure to the full PV system and the opportunity to influence how we continue to develop our safety processes.