Director of Clinical Safety & Pharmacovigilance

Eli Lilly and Company

Indianapolis (IN)

In loco

USD 201.000 - 361.000

Tempo pieno

3 giorni fa
Candidati tra i primi

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Company bonus
401(k) plan
Medical, dental, vision benefits
Life insurance
Well-being benefits

Descrizione del lavoro

Lilly in Indianapolis is seeking a Clinical Research Physician (CRP) within GPS Medical to lead safety assessments across product life cycles. You will collaborate with cross-functional teams to ensure proactive pharmacovigilance and high-quality medical evaluation of safety data.

This role requires MD/DO, board certification in Infectious Disease, 3+ years in pharma or clinical care, and fluent English. You will interact with regulators, discuss risk management, and guide safety surveillance

Competenze

  • MD/DO with board-eligible or board-certified qualifications.
  • US-trained physicians must have board eligibility or certification.
  • Minimum 3+ years in pharma industry or clinical care setting.
  • Board certification in Infectious Disease.

Mansioni

  • Provide GPS Medical leadership and proactive pharmacovigilance for assigned product(s).
  • Oversee safety surveillance activities and risk management actions.
  • Review regulatory queries on safety topics and communicate with stakeholders.
  • Synthesize complex data into actionable safety insights for product teams.
  • Represent GPS Medical in internal and external interactions.

Formazione

MD/DO

Descrizione del lavoro

Lilly in Indianapolis is seeking a Clinical Research Physician (CRP) within GPS Medical to lead safety assessments across product life cycles. You will collaborate with cross-functional teams to ensure proactive pharmacovigilance and high-quality medical evaluation of safety data.

This role requires MD/DO, board certification in Infectious Disease, 3+ years in pharma or clinical care, and fluent English. You will interact with regulators, discuss risk management, and guide safety surveillance

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