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Senior Pharmacovigilance Associate

0-2 years
Not Disclosed
10 Oct. 27, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior Pharmacovigilance Associate

Employer: ICON Strategic Solutions
Location: Mexico (CDMX, Remote / Homeworking)
Salary: Competitive
Start Date: 21 October 2025
Closing Date: 20 November 2025
Contract Type: Full-Time, Permanent
Experience Level: Senior / Experienced


About the Company

ICON plc is a global leader in healthcare intelligence and clinical research. The organization is committed to fostering an inclusive and innovative environment that empowers professionals to shape the future of clinical development and patient safety worldwide.


Role Overview

As a Senior Pharmacovigilance Associate, you will play a key role in ensuring the safety and efficacy of pharmaceutical products. This position involves overseeing pharmacovigilance operations, ensuring compliance with global regulatory requirements, and maintaining the highest standards of data quality and patient safety.
You will also mentor junior staff, lead safety report management, and collaborate with multidisciplinary teams on complex safety evaluations.


Key Responsibilities

  • Lead the collection, evaluation, and processing of adverse event (AE) reports in compliance with regulatory timelines and company SOPs.

  • Perform detailed data analysis and signal detection to identify trends and potential safety issues.

  • Prepare and submit Periodic Safety Update Reports (PSURs) and other safety-related regulatory documents.

  • Collaborate with medical, clinical, and regulatory teams to evaluate the clinical significance of adverse events.

  • Ensure the accuracy and integrity of pharmacovigilance databases and documentation systems.

  • Provide training, guidance, and mentorship to junior PV associates and team members.

  • Participate in audits, inspections, and regulatory reviews, ensuring compliance readiness.

  • Stay informed about emerging pharmacovigilance regulations, international guidelines, and industry best practices.


Candidate Profile

  • Education: Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field (advanced degree preferred).

  • Experience:

    • Substantial experience in pharmacovigilance or drug safety, including case processing, aggregate reporting, and signal management.

    • Deep understanding of regulatory frameworks (ICH, EMA, FDA, etc.).

  • Skills:

    • Strong analytical and problem-solving skills for interpreting safety data.

    • Proficient in pharmacovigilance databases and data management systems.

    • Advanced Microsoft Office Suite proficiency.

    • Excellent communication, documentation, and team collaboration abilities.

    • Proven ability to work independently and manage multiple priorities.

  • Values: High commitment to confidentiality, data accuracy, and patient protection.


What ICON Offers

ICON values its employees as the driving force of innovation and success. The organization promotes high performance, career development, and work-life balance through a competitive and inclusive benefits program.

Example Benefits Include:

  • Generous annual leave entitlements.

  • Comprehensive health insurance coverage for employees and families.

  • Competitive retirement and savings plans for long-term financial security.

  • Access to the Global Employee Assistance Programme (LifeWorks) — 24/7 professional mental health and well-being support.

  • Life assurance coverage.

  • Flexible, country-specific optional benefits such as:

    • Gym membership discounts

    • Bike purchase schemes

    • Subsidized travel passes

    • Health and wellness assessments

    • Childcare vouchers


Commitment to Inclusion

At ICON, inclusion and belonging are core values.
The company is dedicated to building a workplace free from discrimination or harassment, ensuring equal opportunity for all qualified candidates regardless of race, religion, gender, nationality, or disability.


Accommodation Support

Applicants requiring reasonable accommodation due to medical conditions or disabilities may submit a request via ICON’s accessibility portal to ensure equal access during recruitment and employment.


How to Apply

If you’re passionate about advancing patient safety and meet most of the listed requirements, ICON encourages you to apply directly — your unique background may be exactly what the team needs.

  • Current ICON Employees: Please apply via the internal careers portal.

  • External Applicants: Visit the official ICON Careers Website for more opportunities and application details.


Country: Mexico 🇲🇽
Work Type: Remote (CDMX-Based)
Department: Pharmacovigilance / Drug Safety