20 publicaciones de empleo destacadas de total safety en ciudad de méxico, dif (¡Están contratando!)

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Senior Pharmacovigilance Associate
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- Tiempo completo
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Waters Corporation —San Pedro de los Pinos, CDMX
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Schneider Electric —Ciudad de México
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ICON Plc —Ciudad de México, CDMX
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- Administración de personal
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Checkout.com —Ciudad de México, CDMX
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ICON Plc —Ciudad de México, CDMX
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Dover Corporation —Ciudad de México, CDMX
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Distribution Operations
McMaster-Carr —Los Ángeles, CDMX
- Licenciatura
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- Seguro dental
- Vacaciones adicionales o permisos con goce de sueldo
Mexico Major AE
Samsara —Ciudad de México, CDMX
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Medical Affairs Specialist
ICON Plc —Ciudad de México, CDMX
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- Seguro de la vista
Intern Crédito y Cobranza (Polanco, CDMX)
Schneider Electric —Ciudad de México
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- Inglés
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Samsara —Ciudad de México, CDMX
- Home Office (Desde casa)
- Microsoft Excel
- Experiencia en ventas
- Salesforce
- Permiso de maternidad y paternidad

Quiero recibir la alerta de empleo más reciente para total safety en ciudad de méxico, dif

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Senior Pharmacovigilance Associate (Lead)

ICON Plc -
Ciudad de México, CDMX

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Información del empleo

Tiempo completo

Beneficios

Seguro dental
Seguro de la vista

Cualificaciones

Enfermería
Administración de personal
Inglés
Microsoft Office
Experiencia en bases de datos
Licenciatura
Farmacia

Descripción completa del empleo

Pharmacovigilance Associate / Senior Associate

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.

We are currently seeking a Senior Pharmacovigilance Associate to join our diverse and dynamic team. As a Senior Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and efficacy of pharmaceutical products by managing and overseeing pharmacovigilance activities. You will collaborate with cross-functional teams to ensure compliance with regulatory requirements and to maintain the highest standards of patient safety.

Location: Mexico City
Contract type: Hybrid (office-based with flexibility)
Requirement: CVs and assessments must be submitted in English

What You Will Be Doing:

Leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting in accordance with regulatory guidelines and company policies.
Conducting thorough data analysis and interpretation of safety data, identifying trends and potential safety signals that require further investigation.
Preparing and submitting comprehensive periodic safety update reports (PSURs) and other regulatory documents, ensuring compliance with international regulations.
Collaborating with medical and clinical teams to assess the clinical relevance of reported adverse events and contribute to risk management activities.
Overseeing the maintenance and integrity of pharmacovigilance databases, ensuring accurate documentation and compliance with data management standards.
Providing training and mentorship to junior team members on pharmacovigilance processes, regulatory requirements, and best practices.
Engaging in audits and inspections conducted by regulatory authorities, ensuring readiness and compliance with all relevant pharmacovigilance requirements.
Staying informed on evolving regulatory guidelines and industry best practices to continually enhance the pharmacovigilance processes within the organization.

Your Profile:

Bachelor’s degree in life sciences, pharmacy, nursing, or a related field. An advanced degree is preferred.
Experience in leading PV studies or projects (REQUIRED)
Extensive experience in pharmacovigilance or drug safety, with a strong understanding of relevant regulations and industry standards.
Proven ability to manage the pharmacovigilance process effectively, including adverse event reporting and signal detection.
Strong analytical and critical thinking skills, with the ability to interpret complex data and make informed recommendations.
Excellent communication and interpersonal skills, with the ability to work collaboratively across cross-functional teams.
Proficiency in pharmacovigilance databases and data management systems, as well as Microsoft Office Suite.
Ability to work independently and manage multiple priorities in a fast-paced environment.
Commitment to maintaining confidentiality and handling sensitive patient information with discretion.

#LI-FP1

#LI-Hybrid

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

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

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

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