Clinical Research Physician - Global Patient Safety Leader

Regulatory Jobs

Indianapolis (IN)

Vor Ort

USD 246.000 - 361.000

Vollzeit

Vor 7 Tagen
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

401(k)
Pension
Vacation benefits
Medical benefits
Flexible benefits
Life insurance
Time off
Well-being programs

Zusammenfassung

Lilly, headquartered in Indianapolis, Indiana, seeks a Clinical Research Physician for GPS Medical to lead pharmacovigilance and safety oversight across product lifecycles. The role interfaces with product teams, regulators, and external experts to ensure robust safety evaluations and risk management.

Expect strong leadership, deep clinical pharmacovigilance expertise, and the ability to guide cross-functional teams in a fast-paced environment.

Qualifikationen

  • MD or DO; board eligible or certified in relevant specialty.
  • US-trained physicians must have board eligibility or certification; foreign medical graduates may be hired at the discretion of the CMO.
  • Minimum 3+ years' experience in the pharmaceutical industry or clinical care setting.
  • Fluent in English with highly effective written and verbal communication skills.

Aufgaben

  • Provide GPS Medical leadership and ensures proactive pharmacovigilance for assigned product(s).
  • Provide medical oversight of surveillance activities and risk management actions; liaise with stakeholders.
  • Perform medical review of AE/SAE data and support PSA/HHE processes with cross-functional teams.
  • Represent GPS Medical to internal/external stakeholders and regulatory bodies; participate in safety advisory activities.

Kenntnisse

Fluent English
Clinical pharmacovigilance

Ausbildung

MD/DO
Board eligible/certified (US)

Jobbeschreibung

Lilly, headquartered in Indianapolis, Indiana, seeks a Clinical Research Physician for GPS Medical to lead pharmacovigilance and safety oversight across product lifecycles. The role interfaces with product teams, regulators, and external experts to ensure robust safety evaluations and risk management.

Expect strong leadership, deep clinical pharmacovigilance expertise, and the ability to guide cross-functional teams in a fast-paced environment.

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