Global Safety Medical Director - Clinical Program
Hybrid - Cambridge, MA or one of other East Coast Locations
Competitive Compensation Package Based on Experience
$250,000 - $280,000 + Annual Bonus + Equity
SciPro Global is partnered with a Stable & quickly growing Leading life sciences company that is doing incredible work with a pipeline across Therapeutic Areas from Oncology to Infectious Disease to Rare Disease. As they expand their pipeline, there are a few programs in Phase 2 & 3 that require additional Clinical Safety support. This group is ambitious, driven, and motivated to continue being a leader with their successful platform. This position will report directly into the Vice President of Pharmacovigilance and provides unlimited career growth & stability with the technology that they are working on.
Responsibilities include (but not limited to):
Leading clinical safety aggregate reports such as CSR's, DSURs.
Leading risk mitigation and risk minimization measures for global studies.
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.
Clinical Safety experience at a Biotech or Pharmaceutical company.
Aggregate reporting experience on a Global scale, not just individual case review.
Detail Oriented mindset & motivated!
Are you looking to join a brand name company to grow your career?
Apply now to begin the process!