Global Safety Physician & Strategy Lead

TalentAlly

Boston (MA)

Vor Ort

USD 184.000 - 253.000

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Medical/Dental/Vision Insurance
Fitness & Wellness reimbursement
Paid vacation & holidays
401(k) with company match
Stock purchase plan
Tuition reimbursement

Zusammenfassung

Biogen is seeking a Global Safety Physician based in Cambridge, MA, to oversee global pharmacovigilance for investigational and marketed products. You will review safety data, design trials, and manage benefit-risk profiles while representing Safety in internal and external meetings.

The role requires MD with 3+ years in pharma or clinical care, plus pharmacovigilance experience. Competitive compensation and a broad benefits package are offered.

Qualifikationen

  • MD required; subspecialty focus in neuroscience, psychiatry, immunology, rare diseases preferred.
  • Minimum 3+ years' experience in the pharmaceutical industry or clinical care setting; ideally 1+ years of overall experience specific to pharmacovigilance.
  • Prior experience in clinical trials; academic and/or industry.
  • Knowledge of pre- and post- marketing US and EU regulations.

Aufgaben

  • Manage safety surveillance for assigned products and collaborate with PV scientists.
  • Conduct analyses of safety trial data and adverse events handling.
  • Decide on seriousness, expectedness, and causality for safety reports.
  • Provide safety leadership for clinical development programs and regulatory interactions.

Kenntnisse

Leadership
Global collaboration
Clinical development

Ausbildung

MD degree
Neuroscience subspecialty
Psychiatry subspecialty
Rare diseases

Jobbeschreibung

Biogen is seeking a Global Safety Physician based in Cambridge, MA, to oversee global pharmacovigilance for investigational and marketed products. You will review safety data, design trials, and manage benefit-risk profiles while representing Safety in internal and external meetings.

The role requires MD with 3+ years in pharma or clinical care, plus pharmacovigilance experience. Competitive compensation and a broad benefits package are offered.

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