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Graduate Pharmacovigilance Associate

Icon Plc
ICON PLC
0-2 years
Not Disclosed
10 Jan. 12, 2026
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

Job Title: Graduate Pharmacovigilance Associate
Company: ICON Strategic Solutions
Location: Poland (Remote / Homeworking)
Salary: Competitive
Start Date: 9 Jan 2026
Closing Date: 8 Feb 2026

Company Overview:
ICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to improving global health through innovative clinical development solutions. We foster an inclusive environment that drives excellence and innovation, providing a dynamic platform for professional growth and impact in the pharmaceutical and biotechnology sectors.

Position Overview:
We are seeking a Graduate Pharmacovigilance Associate to join our global safety team. The successful candidate will support the monitoring and reporting of adverse events, contributing to the safety and efficacy of pharmaceutical products. This role is ideal for recent graduates with a pharmacy, life sciences, or related background seeking to build a career in pharmacovigilance.

Key Responsibilities:

  • Process adverse event (AE) information in global pharmacovigilance databases using medical knowledge.

  • Conduct quality control of entered data to ensure consistency, accuracy, and regulatory compliance.

  • Collaborate with international teams to maintain high-quality reporting standards and optimize work efficiency.

  • Support projects aimed at enhancing pharmacovigilance and clinical data management processes.

  • Participate in training programs to gain in-depth understanding of pharmacovigilance practices and regulatory guidelines.

Qualifications and Skills:

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

  • Strong attention to detail, organizational skills, and ability to manage multiple tasks.

  • Excellent written and verbal communication skills in English; proficiency in Polish required.

  • Knowledge of medical terminology and clinical/pharmacovigilance concepts is desirable but not mandatory.

  • Proficiency in Microsoft Office and analytical problem-solving skills.

  • French language proficiency is an advantage.

Experience:

  • Entry-level / Graduate. Relevant internships or exposure to clinical research/pharmacovigilance is a plus.

Why Join ICON:

  • Opportunity to work with a globally recognized CRO on international pharmacovigilance projects.

  • Inclusive and supportive work environment that values diversity and employee development.

  • Comprehensive benefits package, including health insurance, retirement plans, flexible work options, employee assistance programs, and life assurance.

  • Professional growth opportunities with training and mentoring in global pharmacovigilance and clinical safety.