Pharmacovigilance Supervisor

ICON; A distancia; MXN 200,000 - 400,000; Jornada completa

Descripción de la vacante

A global healthcare organization in Mexico City seeks a Supervisor, Pharmacovigilance to oversee safety monitoring for clinical trials. The role involves managing day-to-day pharmacovigilance operations, ensuring compliance with regulatory standards, and leading a team in effective safety reporting. The ideal candidate will hold a Bachelor’s degree in life sciences or pharmacy, possess experience in drug safety, and demonstrate strong leadership and communication skills. This position offers competitive salary and diverse benefits focused on well-being and work-life balance.

Servicios

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Formación

• Experience in pharmacovigilance or drug safety, focusing on clinical trials or post-marketing surveillance.
• Strong knowledge of global pharmacovigilance regulations and guidelines.
• Ability to manage multiple tasks and ensure accuracy in safety reporting.

Responsabilidades

• Supervise the day-to-day pharmacovigilance operations.
• Collaborate with cross-functional teams to optimize pharmacovigilance processes.
• Ensure compliance with global regulatory requirements.

Conocimientos

Leadership

Attention to detail

Communication skills

Educación

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

Descripción del empleo

Home Based - CDMX

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.
• 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.

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.