Global Safety Director (Multiple Openings)
Competitive Compensation Package Based on Experience
$290,000 - $350,000 + Annual Bonus + Pension
SciPro Global is exclusively partnered with a Stable & quickly growing company that is doing incredible work with a pipeline across Therapeutic Areas from Oncology to Immunology to CNS to Cardiometabolic. As they expand their pipeline, there are over 30 programs in Phase 1 & 2 right now leading to multiple positions opening up in their Safety group. This group is solution oriented and full of team players, while being led by a direct, passionate, and impressive leader in the US. This position will report directly into the Therapeutic Area Safety Head of the aligning Therapeutic Area and provides unlimited career growth & stability with the technology that they are working on.
Responsibilities include (but not limited to):
Safety analysis of both clinical trials & post marketed products.
Leading clinical safety aggregate reports such as 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 10 years Pharmacovigilance and Safety experience.
Either board certification with patient facing experience or 2 years of Pharmacovigilance & Safety experience at a Biotech or Pharma,.
Solution Oriented mindset & motivated!
Are you looking to join a brand name company to grow your career?
Apply now to begin the process!