Medical Director Safety & Pharmacovigilance
Hybrid - Massachusetts
Competitive Compensation Package Based on Experience
$245,000 - $290,000 + Annual Bonus + Stocks
SciPro Global is currently partnered with an exciting Solid Tumor company that has both marketed products and cutting edge clinical trials going on. With a collaborative Safety group that is focused on honesty and making groundbreaking strides in science, they are looking to bring in a Medical Director Pharmacovigilance to their team. You'll be focused on their early phase solid tumor trial and reporting directly to the Senior Medical Director Pharmacovigilance. Having a hiring manager with impressive tenure in the space, you'll receive superb mentorship while in this role too.
Responsibilities include (but not limited to):
Leading on aggregate reports for early phase programs
Provide Safety expertise for assigned products in the pipeline
Safety analysis of both clinical trials & post marketed products
Leading benefit risk assessment activities
Leading on Safety Signaling and Signal Management
Lead signal managements & safety surveillance alongside team members directly working on these
Cross functional collaboration with Clinical Development team for plans and protocol design
Represent safety team with senior leadership within company
Present to external stakeholders on safety data
Leading Safety Management Team meetings & driving strategy within program
Provide labeling input
Responding to health authority queries regarding safety & risk sections of regulatory documents
Requirements include (but not limited to):
Medical Director or Foreign Equivalent
Minimum 3 years in Safety or Pharmacovigilance within a Biotech or Pharma
Oncology or Rare Disease experience preferred
Are you looking to joining a cutting edge company?
Apply now to begin the process!