Associate Medical Director, Global Drug Safety (Cambridge)

Responsibilities

• Global pharmacovigilance for investigational and/or marketed products
• Review and analyze safety data
• Design clinical trials
• Identify and investigate safety signals
• Manage the benefit-risk profile for assigned compounds and products

Qualifications

• Proven leader in safety & pharmacovigilance; develops and advances successful programs across multiple development phases
• Experience working/leading high-performing teams with guidance and mentoring

Required Skills

• MD or MD/PhD required
• 3+ years of experience in the pharmaceutical industry or clinical care setting (ideally pharmacovigilance)

Preferred Skills

• Prior experience in clinical trials (academic and/or industry)
• Knowledge of pre- and post-marketing US and EU regulations

Benefits

• Base compensation range: $194,000.00-$267,000.00
• Medical, Dental, Vision, and Life insurances
• Fitness & Wellness programs including fitness reimbursement
• Short- and Long-Term Disability insurance
• Paid vacation (minimum 15 days) and end-of-year shutdown time off (Dec 26–Dec 31)
• Up to 12 company paid holidays + 3 paid days off for Personal Significance
• 80 hours of sick time per calendar year
• Paid Maternity and Parental Leave
• 401(k) with company matched contributions
• Employee stock purchase plan
• Tuition reimbursement up to $10,000 per calendar year
• Employee Resource Groups participation