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Graduate Pharmacovigilance Associate

0-2 years
$300,000 – $420,000 per year
10 May 23, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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: Graduate Pharmacovigilance Associate
Employer: ICON Strategic Solutions
Location: Mexico, Homeworking
Salary: Competitive

Job Summary:
As a Graduate Pharmacovigilance Associate, you will join the world’s largest and most comprehensive clinical research organization. Powered by healthcare intelligence, you will support pharmacovigilance activities including safety data processing, literature review, and safety reporting for pharmaceutical and medical device products. This is an excellent opportunity for recent graduates to gain experience in a global drug safety environment.

Key Responsibilities:

  • Review and process safety events for pre- and post-marketing products including medical devices and drugs

  • Analyze abstracts and full articles for safety information from literature sources

  • Generate data listings from safety databases and ensure data accuracy

  • Conduct adverse event follow-ups via written correspondence or phone

  • Maintain accuracy of safety tracking systems and assist with project documentation

  • Review clinical and diagnostic data for safety concerns during case processing

  • Liaise with investigators, reporters, and sponsors regarding safety issues

  • Participate in team meetings and teleconferences as needed

  • Respond to medical information inquiries, including adverse events and product complaints

  • Handle safety and quality complaints in accordance with client-specific instructions

  • Submit expedited SAE reports, periodic reports, and safety data to clients and regulatory bodies as required

  • Support filing activities in the electronic Trial Master File (eTMF)

  • Ensure readiness for audits or inspections on assigned projects

Qualifications:

  • Bachelor’s degree in health sciences, life sciences, or a related field

  • Some experience in the pharmaceutical industry, preferably in pharmacovigilance or drug safety

  • Knowledge of medical terminology and coding systems

  • Proficiency in English and the language of the host country

What ICON Offers:

  • Competitive salary and country-specific benefits

  • Annual leave entitlement

  • Health insurance options for employees and families

  • Retirement planning options

  • Global Employee Assistance Programme (TELUS Health)

  • Life assurance

  • Optional benefits: childcare vouchers, gym memberships, travel passes, and more

Inclusion & Accessibility:
ICON is committed to fostering an inclusive, accessible, and diverse work environment. Reasonable accommodations are available throughout the hiring process and employment.

Estimated Salary:
Based on similar entry-level pharmacovigilance roles in Mexico: MXN $300,000 – $420,000 per year