Pharmacovigilance Associate (Brazil, Hybrid Mode)

Nextrials, Inc.; São Paulo; Presencial; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

Nextrials, Inc. is seeking a dedicated Pharmacovigilance Associate to join their dynamic team. The role includes monitoring pharmaceutical safety, collecting and analyzing adverse event reports, and ensuring compliance with regulatory guidelines. This is an entry-level position offering competitive salary and benefits in a supportive environment.

Serviços

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Employee Assistance Programme

Flexible optional benefits

Qualificações

• Experience in pharmacovigilance (case processing), drug safety, or related area is preferred.
• Commitment to high standards of quality and compliance.

Responsabilidades

• Collect and review adverse event reports.
• Conduct signal detection and risk assessment activities.
• Assist in the preparation of safety reports and regulatory submissions.

Conhecimentos

Analytical skills

Attention to detail

Communication

Interpersonal skills

Formação académica

Bachelor's degree in life sciences, pharmacy, or a related field

Advanced degree preferred

Descrição da oferta de emprego

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ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. Your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance.

What You Will Be Doing

• Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines.
• Conducting signal detection and risk assessment activities to identify potential safety issues.
• Collaborating with cross-functional teams to support safety-related inquiries and investigations.
• Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices.
• Assisting in the preparation of safety reports and regulatory submissions.
  
  

Your Profile

• Bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred.
• Experience in pharmacovigilance (case processing), drug safety, or a related area, preferably within a clinical or pharmaceutical environment.
• Strong analytical skills with attention to detail in data collection and reporting.
• Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders.
• A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities.
  
  

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
  
  

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Software Development

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