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Graduate Pharmacovigilance Associate

0-2 years
Not Disclosed
10 Oct. 31, 2025
Job Description
Job Type: Full Time 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

Graduate Pharmacovigilance Associate

📍 Location: Mexico (Home-based, CDMX)
🏢 Employer: ICON Strategic Solutions
💼 Job Type: Full-time
💰 Salary: Competitive
🗓️ Start Date: 28 October 2025
Closing Date: 27 November 2025


About ICON

ICON plc is a world-leading healthcare intelligence and clinical research organization. We are dedicated to advancing clinical development through innovation, data-driven insights, and operational excellence.
At ICON, we foster an inclusive and collaborative environment where every individual contributes to shaping the future of global healthcare.


About the Role

The Graduate Pharmacovigilance Associate will play a vital role in supporting the safety monitoring and reporting of pharmaceutical products.
This entry-level role provides an excellent opportunity for recent graduates in life sciences or pharmacy to begin a rewarding career in Pharmacovigilance (PV) — the science of monitoring, assessing, and preventing adverse effects of drugs.

You will assist in the collection, analysis, and communication of safety data in compliance with global regulatory requirements and company procedures.


Key Responsibilities

  • Support the collection, review, and processing of adverse event (AE) data in accordance with pharmacovigilance regulations and company SOPs.

  • Assist in the preparation and submission of safety reports to regulatory authorities and stakeholders.

  • Collaborate with cross-functional teams (e.g., clinical, regulatory, and safety operations) to ensure timely and accurate communication of safety information.

  • Contribute to the development and maintenance of pharmacovigilance documentation, including SOPs and Safety Management Plans.

  • Participate in training and professional development programs to deepen knowledge of pharmacovigilance practices, global safety standards, and regulatory frameworks.


Candidate Profile

  • Education: Bachelor’s degree in Pharmacy, Life Sciences, or a related discipline.

  • Skills & Attributes:

    • Strong attention to detail and organizational ability.

    • Capable of managing multiple priorities effectively.

    • Excellent communication and interpersonal skills.

    • Proficiency in Microsoft Office (Word, Excel, PowerPoint).

    • Good analytical and problem-solving abilities.

  • Knowledge (Preferred but not required):

    • Basic understanding of pharmacovigilance principles and regulatory guidelines.

    • Relevant training will be provided for fresh graduates.


What ICON Offers

At ICON, we believe that our success depends on our people. We provide a supportive environment that encourages career growth, well-being, and work-life balance.

Benefits include (varies by country):

  • Competitive salary and annual leave entitlements

  • Comprehensive health insurance options for employees and families

  • Retirement and savings plans for long-term financial security

  • Access to LifeWorks Global Employee Assistance Programme (EAP) — 24/7 confidential support for employees and families

  • Life assurance and optional country-specific benefits, such as:

    • Childcare vouchers

    • Bike purchase schemes

    • Discounted gym memberships

    • Subsidized travel passes

    • Health assessments and wellness programs


Diversity, Inclusion & Accessibility

ICON is committed to equality, inclusion, and belonging.
We provide a discrimination-free workplace where all qualified applicants are considered regardless of race, gender, sexual orientation, gender identity, religion, national origin, disability, or veteran status.

If you require reasonable accommodation due to a disability or medical condition during the application process, please let us know via the official ICON support channel.


💬 Why Join ICON?

  • Global exposure in a top-tier CRO

  • Structured training and mentoring for graduates

  • Opportunities for career growth in Pharmacovigilance and Drug Safety

  • A culture of collaboration, learning, and inclusivity


Application Information

  • Interested but not sure if you meet all requirements? Apply anyway! ICON encourages applications from individuals with potential — we value passion and curiosity as much as experience.

  • Current ICON employees should apply via the internal career portal.

📢 Apply Now to start your journey as a Graduate Pharmacovigilance Associate and make an impact on global patient safety.