(Senior) Patient Safety Physician, Medical Safety Physician - Oncology
$280,000–$280,000 year
Remote
Job Summary
Develop or support proactive risk management strategies for marketed and investigational compounds globally. Chair or support the BI-internal Asset Benefit Risk Team and lead medical-scientifically directed teams of risk management physicians, including project-specific training and coaching. Provide updates of the assigned drug's safety profile to senior management and recommend pharmacovigilance activities to BI decision-making bodies and the EU QPPV. Represent PSPV in internal, external, and global health authority committees while contributing to strategic projects on future software solutions and regulatory developments. This Director-level role requires over five years of total experience, including two years in the pharmaceutical industry, with a strong emphasis on people leadership and influencing teams. The position offers a base salary between $280,000 and $441,000 and includes eligibility for a variable or performance-based bonus.
Required Qualifications
- US MD or DO degree or international equivalent from an accredited institution
- Completion of a US residency or ex-US equivalent
- Active or inactive US license to practice medicine, or international equivalent
- Board certification / experience in a medicine subspecialty
- People leadership potential
- Total applicable experience (incl. clinical practice, plus research or relevant industry) of greater than three (3) years
- Total applicable experience (incl. clinical practice, research or relevant industry) of greater than five (5) years
- Minimum of two (2) years of experience in the pharmaceutical industry or equivalent (preferably pharmacovigilance)
- One to three (1-3) years of leadership experience (e.g. projects, teams, initiative) and influencing teams
- Excellent interpersonal and communication skills (both written and oral)
- Ability to attend key meetings in person
- Highly ethical personality putting patient safety first
- Self-starter and driving personality, willingness to take on responsibilities
- Sound medical-scientific and clinical knowledge and judgement
- Ability to synthesize large amounts of medical data, draw medical conclusions, and clearly communicate the conclusions
- Good understanding (based on experience) of Pharmacovigilance and Risk Management in a major pharmaceutical company on a global / corporate level, including safety in clinical development and post-marketing safety
- Understanding of pharmacovigilance regulation in major markets and respective need for compliance
Desired Qualifications
- Completion of a US residency or ex-US equivalent
- Active or inactive US license to practice medicine, or international equivalent
- Board certification / experience in a medicine subspecialty would be an asset
- Total applicable experience (incl. clinical practice, plus research or relevant industry) of greater than three (3) years
- Total applicable experience (incl. clinical practice, research or relevant industry) of greater than five (5) years, and a minimum of two (2) years of experience in the pharmaceutical industry or equivalent (preferably pharmacovigilance)
- One to three (1-3) years of leadership experience (e.g. projects, teams, initiative) and influencing teams
- Good understanding (based on experience) of Pharmacovigilance and Risk Management in a major pharmaceutical company on a global / corporate level, including safety in clinical development and post-marketing safety
- Understanding of pharmacovigilance regulation in major markets and respective need for compliance
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.