Pharmacovigilance Physician
$280k - 320k per year
Clinical
United States
Permanent
Remote

 

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!

(Hier) Bewerben
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Global Safety Medical Director
United States

 Global Safety Medical Director REMOTECompetitive Compensation Package Based on Experience SciPro Global is exclusively partnered with a Stable & quickly growing Pharmaceutical company that is doing incredible work with a pipeline across Therapeutic Areas from Oncology to Cardiovascular to Immunology to CNS to Respiratory. As they expand their pipeline, there are over 30 programs in Phase 1 & 2 right now which has led to massive growth in their Safety group. This team 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 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 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 7 years of Pharmacovigilance & Safety experience at a Biotech or Pharma.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!

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