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Pharmacovigilance Scientist

2+ years
Not Disclosed
10 Dec. 5, 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

Pharmacovigilance Scientist

Location: Mexico (Home-Based) | Experience Required: 2+ Years
Apply by: 3 January 2026 | Start Date: 4 December 2025**

Employer: ICON Strategic Solutions
Employment Type: Full-Time
Work Model: Remote (Mexico)
Industry: Clinical Research / Drug Safety
Compensation: Competitive


About the Company

ICON Strategic Solutions, part of ICON plc, is a global leader in healthcare intelligence and clinical research. The organization is committed to advancing innovation, maintaining the highest standards of scientific integrity, and creating an inclusive work culture that supports professional growth. As a key contributor to ICON’s mission, you will help shape the future of global clinical development and patient safety.


Position Overview

ICON is seeking an experienced Pharmacovigilance Scientist to join its global team. The role focuses on monitoring the safety profile of pharmaceutical products by evaluating, interpreting, and reporting adverse event data in accordance with global regulatory expectations.

This job post is optimized for worldwide search visibility, SEO performance, and GPT-based discoverability to help experienced pharmacovigilance professionals find relevant global opportunities.


Key Responsibilities

  • Collect, review, and evaluate adverse event reports to ensure accurate and timely regulatory submissions.

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

  • Provide scientific input to cross-functional teams on safety inquiries, regulatory questions, and ongoing investigations.

  • Prepare high-quality safety documentation including periodic reports, expedited submissions, and regulatory filings.

  • Maintain thorough understanding of evolving global pharmacovigilance guidelines and industry standards.

  • Support the continuous improvement of pharmacovigilance systems, documentation, and operational frameworks.


Required Qualifications and Experience

Education:

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

  • Advanced degree (Master’s or higher) preferred but not mandatory.

Experience Required:

  • Minimum 2 years of experience in pharmacovigilance, drug safety, clinical research, or a related discipline.

  • Prior experience in case processing, safety surveillance, or regulatory reporting is strongly preferred.

Skills:

  • Strong analytical and scientific evaluation capabilities.

  • High attention to detail in data assessment and documentation.

  • Excellent communication and interpersonal skills to collaborate with cross-functional teams.

  • Ability to work independently in a structured, compliance-driven environment.


What ICON Offers

ICON’s employee benefits are designed to promote well-being, professional growth, and work–life balance. Benefits may vary by country but typically include:

  • Competitive compensation packages

  • Generous annual leave entitlements

  • Comprehensive health insurance options

  • Retirement planning benefits

  • Global Employee Assistance Program (LifeWorks)

  • Life assurance coverage

  • Flexible optional benefits, such as gym memberships, childcare support programs, travel schemes, wellness assessments, and more

For detailed country-specific benefits, candidates may visit ICON’s official careers portal.


Commitment to Inclusion and Equal Opportunity

ICON is dedicated to creating an inclusive, accessible, and harassment-free workplace. All qualified applicants will be considered without regard to gender, ethnicity, nationality, disability, or veteran status. Candidates requiring accommodation during the application process may request appropriate support.

If you believe you meet most, but not all, of the listed requirements, you are encouraged to apply. ICON values diverse experience and transferable skills.


Application Deadline

Apply by: 3 January 2026