Pharmacovigilance Physician - Oncology
REMOTE
Competitive Compensation Package Based on Experience
SciPro Global is exclusively partnered with an Oncology biotech with promising science that is growing their Safety group as their pipeline progresses. This is the second hire for this group, reporting directly into the Vice President of Safety, and individual who is a calm leader with strong abilitiy to train their team.
Responsibilities include (but not limited to):
- Safety analysis of both clinical trials & post marketed products.
- Leading clinical safety aggregate reports such PADERs.
- Leading risk mitigation and risk minimization measures for global studies, specifically working with RMPs.
- Responding to health authority queries regarding safety & risk sections of regulatory documents.
- Perform signal management & lead signal strategy measures.
- Safety surveillance of all assigned products.
- Cross functionally act as Safety SME for assigned products & liaise with other Clinical counterparts across the organization.
- Communicate safety updates with external & internal stakeholders.
- Provide safety input for clinical study design activities.
- Identify ways of improvement for team & safety group.
Requirements include (but not limited to):
- Medical Director or Foreign Equivalent.
- Minimum 3 years of Pharmacovigilance & Safety experience at a Biotech or Pharma.
- Oncology Experience required.
- Management experience.
- Solution Oriented mindset & motivated!
Are you looking to join a brand name company to grow your career?
Apply now to begin the process!
Need more help? Reach out<br></br> to one of our team.
We are a trusted partner for every step from Discovery through to Development. So, no matter where you are in your journey, we're here to help you make a difference. We are a trusted partner for every step from Discovery through to Development. So, no matter where you are in your journey, we're here to help you make a difference.
