Senior Manager Pharmacovigilance

 Posted 6 days ago
  
 Brazil
  
5-10 years experience
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AI Summary

Oversee pharmacovigilance and drug safety operations to ensure the safety and efficacy of clinical trials. Manage the safety team to ensure accurate reporting of adverse events and implement policies to enhance risk management.
CDMX - People Lead

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Senior Manager, Pharmacovigilance at ICON, you will be responsible for overseeing pharmacovigilance activities to ensure the safety and efficacy of our clinical trials.

What You Will Do:

You will oversee pharmacovigilance and drug safety operations, balancing quality, timelines, and stakeholder expectations.

Key responsibilities include:

  • Managing the pharmacovigilance team to ensure timely and accurate reporting of adverse events and safety data in compliance with regulatory standards.
  • Developing and implementing pharmacovigilance policies and procedures to enhance safety monitoring and risk management practices.
  • Collaborating with cross-functional teams, including clinical operations and regulatory affairs, to ensure integration of safety data into clinical development plans.
  • Monitoring and analyzing safety data trends to identify potential risks and inform decision-making for ongoing clinical trials.
  • Staying updated on industry regulations and best practices in pharmacovigilance to drive continuous improvement initiatives.

Your Profile:

You will have a strong background in pharmacovigilance and drug safety, with proven management experience and a commitment to quality delivery.

Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Significant experience in pharmacovigilance or drug safety, ideally within the clinical research or pharmaceutical industries.
  • Strong understanding of regulatory requirements related to drug safety and reporting.
  • Excellent analytical and problem-solving skills, with a focus on data-driven decision-making.
  • Strong communication and interpersonal skills, capable of engaging and influencing diverse stakeholders.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

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