Medical Director Pharmacovigilance
$245,000 - 290,000 + Annual Bonus + Stocks
Massachusetts, USA

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!

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