Pharmacovigilance Reporting Associate (Intelligence)

ICON Clinical Research; Ciudad de México; Híbrido; MXN 360.000 - 540.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance

Retirement planning

Global Employee Assistance Programme

Life assurance

Descripción de la vacante

ICON Clinical Research is seeking a Pharmacovigilance Reporting Associate (Intelligence) to prepare safety reports for clinical trials and post‑marketing activities. You will operate as a safety reporting intelligence processor or lead, ensuring timely submissions and compliance while aligning with ICON values of people, clients and performance.

The role emphasizes collaboration within multidisciplinary teams, adherence to SOPs, and a focus on process improvement to streamline workflows and add

Formación

• Experience in pharmacovigilance or drug safety with an understanding of safety reporting processes and regulatory requirements.
• Excellent attention to detail and organizational skills.
• Strong communication and collaboration abilities in a multidisciplinary team.
• Ability to manage multiple tasks in a fast-paced, regulated environment.

Responsabilidades

• Serve as safety reporting intelligence processor and lead on multiple projects.
• Adhere to ICON values centering on People, Clients and Performance.
• Contribute to process improvements to streamline workflows and add value.
• Complete departmental project activities accurately per ICON SOPs and procedures.
• Handle safety reporting activities with a customer-focused mindset and audit readiness.
• Demonstrate skills in client management, safety reporting, project scope, submission compliance, quality and budgeting.

Conocimientos

Pharmacovigilance

Attention to detail

Communication

Multitasking

Team collaboration

Educación

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

Descripción del empleo

Pharmacovigilance Reporting Associate (Intelligence)

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 Pharmacovigilance Reporting Associate at ICON, you will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities.

What You Will Do:

• Serve as safety reporting intelligence processor and/or lead for multiple safety reporting or safety reporting intelligence stand‑alone projects, providing management support as designated.
• Recognize, exemplify, and adhere to ICON's values, which center around our commitment to People, Clients, and Performance.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
• Complete all departmental project activities accurately in accordance with ICON SOPs, Study Specific Procedures, regulatory requirements, and client processes.
• Responsible for safety reporting or safety reporting intelligence activities on assigned projects, working in a customer focused approach and an audit and inspection ready mindset.
• Demonstrate skills pertaining to client management, safety reporting, project scope, submission compliance, quality, and budget.

Your Profile

• Bachelor's degree in life sciences, pharmacy, or a related field.
• Experience in pharmacovigilance or drug safety, with an understanding of safety reporting processes and regulatory requirements preferred.
• 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.

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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 (https://careers.iconplc.com/benefits) 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 (https://careers.iconplc.com/reasonable-accommodations)