Associate Director - Patient Safety Risk Management

December 14

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Description

• Contribute to long-term benefit-risk assessment of cell therapy products. • Design and conduct long-term follow-up clinical trials and post-authorization safety studies. • Collaborate with internal and external partners. • Manage complex timelines and provide mentorship.

Requirements

• PharmD/PhD in life sciences or related field with 5+ years’ experience or MA/MS/MBA with 8+ years’ experience or BA/BS with 10+ years’ experience. • Significant drug safety experience preferred. • Knowledge of worldwide PV regulations. • Understanding of observational studies in pharmacoepidemiology.

Benefits

• Company-sponsored medical, dental, vision, and life insurance plans. • Discretionary annual bonus. • Discretionary stock-based long-term incentives. • Paid time off.

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🇺🇸 United States – Remote

💵 $140k - $170k / year

💰 $110M Series D on 2021-07

⏰ Full Time

🟠 Senior

🎲 Risk

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