Pharmacovigilance Coordinator - Post Marketing (FSP - Sponsor Dedicated)

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

Resumo da oferta

A leading clinical research organization in São Paulo is seeking a Pharmacovigilance Coordinator to oversee safety monitoring and report adverse events related to clinical trials and marketed products. The ideal candidate will have a Bachelor's degree in life sciences or pharmacy, experience in pharmacovigilance, and strong leadership skills. Responsibilities include supervising operations, ensuring compliance with regulations, and training the team. This role offers competitive compensation and a range of benefits focused on employee well-being and work-life balance.

Serviços

Health insurance offerings

Competitive retirement planning

Flexible optional benefits

Global Employee Assistance Programme

Annual leave entitlements

Qualificações

• Bachelor’s degree in life sciences, pharmacy, or a related field.
• Experience in pharmacovigilance or drug safety, preferably in clinical trials.
• Strong knowledge of global pharmacovigilance regulations.
• Detail-oriented with the ability to manage multiple tasks.

Responsabilidades

• Supervise pharmacovigilance operations and report adverse events.
• Collaborate with cross-functional teams for process optimization.
• Ensure compliance with regulatory requirements.
• Manage safety data collection and submission.
• Provide leadership and training to the pharmacovigilance team.

Conhecimentos

Leadership

Team management

Attention to detail

Strong communication skills

Pharmacovigilance knowledge

Regulatory compliance

Fluent English

Formação académica

Bachelor’s degree in life sciences or pharmacy

Descrição da oferta de emprego

Pharmacovigilance Coordinator - Post Marketing (FSP - Sponsor Dedicated)

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 Supervisor, Pharmacovigilance to join our diverse and dynamic team. As a Supervisor, Pharmacovigilance at ICON, you will play a pivotal role in overseeing the safety monitoring and reporting of adverse events related to clinical trials and marketed products. You will contribute to ensuring patient safety and regulatory compliance through effective management of pharmacovigilance activities, coordination with cross‑functional teams, and maintaining the highest standards of safety reporting.

What You Will Be Doing:

• Supervising the day‑to‑day pharmacovigilance operations, ensuring timely and accurate reporting of adverse events.
• Collaborating with cross‑functional teams, including clinical operations and regulatory affairs, to optimize pharmacovigilance processes.
• Ensuring compliance with global regulatory requirements and internal standard operating procedures for safety reporting.
• Managing safety data collection, analysis, and submission to regulatory authorities.
• Providing leadership and training to the pharmacovigilance team, ensuring adherence to best practices in safety monitoring.

Your Profile:

• Bachelor’s degree in life sciences, pharmacy, or a related field.
• Experience in pharmacovigilance or drug safety, with a focus on clinical trials or post‑marketing surveillance.
• Experience leading teams or projects.
• Strong knowledge of global pharmacovigilance regulations and guidelines.
• Excellent communication, leadership, and organizational skills, with the ability to manage a team effectively.
• Detail‑oriented with the ability to manage multiple tasks and ensure accuracy in safety reporting.
• Fluent English (conversation, reading and writing).

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, subsidised 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.