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Pharmacovigilance Scientist

1-2 years
Not Disclosed
10 Dec. 12, 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

Pharmacovigilance Scientist – Home-Based (Mexico)

Employer: ICON Strategic Solutions
Location: Mexico (Remote)
Job Type: Full-Time | Permanent
Discipline: Clinical Research, Pharmacovigilance
Experience Level: Experienced (Non-Manager)
Start Date: 4 December 2025
Closing Date: 3 January 2026


About the Role

ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Pharmacovigilance Scientist to join its expanding safety team. This role supports the safety monitoring of pharmaceutical products by analyzing adverse event data, interpreting safety signals, and ensuring regulatory compliance. The position is fully remote and open to candidates located in Mexico.

This opportunity is ideal for professionals with strong analytical capabilities, pharmacovigilance experience, and a commitment to advancing drug safety in clinical development and post-marketing environments.


Key Responsibilities

  • Perform collection, triage, review, and assessment of adverse event reports in accordance with global regulatory requirements.

  • Conduct signal detection activities and risk assessments to identify emerging safety concerns.

  • Support cross-functional teams by responding to safety-related questions and participating in investigations.

  • Prepare, contribute to, and submit safety reports, regulatory documents, and periodic updates within required timelines.

  • Maintain up-to-date knowledge of global pharmacovigilance regulations, compliance standards, and industry best practices.


Required Qualifications

Education

  • Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Biotechnology, or a related field.

  • Advanced degree (Master’s or higher) preferred.

Experience

  • Minimum 1–2 years of experience in Pharmacovigilance, Drug Safety, Clinical Research, or related functions.

  • Experience with case processing, safety data analysis, or regulatory reporting preferred.

  • Familiarity with global safety databases and pharmacovigilance workflows beneficial.

Skills

  • Strong analytical and problem-solving abilities for safety data evaluation.

  • High attention to detail and accuracy in documentation and reporting.

  • Excellent written and verbal communication skills for effective collaboration with global teams.

  • Ability to work in a regulated environment with strict deadlines and compliance requirements.


What ICON Offers

ICON provides a performance-driven environment designed to support career growth, innovation, and work-life balance. Benefits may include:

  • Competitive compensation tailored to the country of employment

  • Comprehensive annual leave options

  • Health insurance packages for you and your family

  • Retirement planning programs

  • Global Employee Assistance Programme (LifeWorks)

  • Life assurance

  • Optional country-specific benefits such as childcare support, wellness programs, gym discounts, subsidized travel, and more

Visit ICON’s careers portal for additional details on country-specific benefits.


Inclusive Workplace Commitment

ICON promotes a diverse, inclusive, and accessible work environment. All qualified applicants are considered without discrimination. Reasonable accommodations are available for candidates with disabilities throughout the hiring process.