Pharmacovigilance Reporting Associate (Brazil, Hybrid Mode)

ICON; São Paulo; Híbrido; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

ICON, a leading healthcare intelligence and clinical research organization, is seeking a Pharmacovigilance Reporting Associate. This role involves monitoring the safety of pharmaceutical products, preparing comprehensive safety reports, and collaborating with cross-functional teams. The ideal candidate will have a bachelor's degree in life sciences or pharmacy and experience in pharmacovigilance, bringing strong analytical and communication skills to ensure patient safety and compliance with regulatory standards.

Serviços

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible country-specific optional benefits

Qualificações

• Experience in pharmacovigilance or drug safety with knowledge of regulatory requirements.
• Strong understanding of safety reporting processes and attention to detail.

Responsabilidades

• Preparing and reviewing safety reports for accuracy and compliance.
• Collecting and analyzing adverse event data from clinical trials.
• Ensuring timely submission of safety reports to regulatory authorities.

Conhecimentos

Attention to Detail

Organizational Skills

Analytical Skills

Communication

Collaboration

Formação académica

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

Advanced degree preferred

Descrição da oferta de emprego

Pharmacovigilance Associate (Brazil, Hybrid Mode)

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 Reporting 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:

• Preparing and reviewing safety reports, including periodic safety updates and individual case safety reports, ensuring accuracy and compliance with regulatory standards.
• Collecting and analyzing adverse event data from clinical trials and post-marketing sources to support the preparation of comprehensive safety reports.
• Maintaining up-to-date knowledge of regulatory requirements and industry best practices related to pharmacovigilance reporting.
• Collaborating with cross-functional teams, including clinical, regulatory, and data management, to gather necessary information and resolve any reporting issues.
• Ensuring the timely submission of safety reports to regulatory authorities and sponsors, adhering to established deadlines and guidelines.

Your Profile to be Associate:

• Bachelor’s degree in life sciences, pharmacy, or a related field.
• Experience in pharmacovigilance or drug safety, with a strong understanding of safety reporting processes and regulatory requirements.
• Excellent attention to detail and organizational skills, with the ability to prepare and review complex safety reports accurately.
• Strong communication and collaboration skills, with experience working effectively within a multidisciplinary team.
• Ability to manage multiple tasks and prioritize effectively in a fast-paced, regulated environment.

Your Profile:

• Bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred.
• Experience in pharmacovigilance (reporting/submissions), 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.

#LI-FP1

#LI-Hybrid

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