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Mex - Pharmacovigilance Reporting (Associate & Senior Associate)

0-2 years
Not Disclosed
10 April 29, 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

MEX - Pharmacovigilance Reporting (Associate & Senior Associate)
Employer: ICON Plc
Location: Mexico, Homeworking (Mexico City office-based average 3 days/week)
Salary: Competitive
Start Date: 23 April 2025
Closing Date: 23 May 2025


About ICON Plc:

ICON plc is a global leader in healthcare intelligence and clinical research. We are committed to driving innovation, fostering inclusivity, and delivering excellence in clinical development. Join us in shaping the future of healthcare.


Position Overview:

ICON is hiring for Pharmacovigilance Reporting Associates and Senior Associates to join our Pharmacovigilance team in Mexico. The role involves accurate and timely preparation of safety reports for clinical trials and post-marketing activities, ensuring strict compliance with global regulatory requirements.


Key Responsibilities:

  • Prepare and review safety reports (e.g., periodic safety updates, individual case safety reports) ensuring regulatory compliance.

  • Analyze adverse event data from clinical trials and post-marketing sources to produce comprehensive safety documentation.

  • Stay current with global regulatory requirements and pharmacovigilance best practices.

  • Collaborate with clinical, regulatory, and data management teams to resolve reporting issues.

  • Submit safety reports to regulatory bodies and sponsors in accordance with deadlines and procedures.


Qualifications for Associate Role:

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

  • Experience in pharmacovigilance or drug safety.

  • Strong knowledge of safety reporting procedures and regulations.

  • High attention to detail and excellent organizational skills.

  • Effective communication and teamwork abilities.

  • Ability to multitask in a fast-paced, regulated environment.


Qualifications for Senior Associate Role:

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

  • Extensive experience in pharmacovigilance or drug safety.

  • Demonstrated experience in leading projects or studies.

  • Strong knowledge of regulatory requirements and safety processes.

  • High level of accuracy in reviewing complex safety reports.

  • Proven leadership and collaboration skills across cross-functional teams.

  • Ability to prioritize tasks and manage workload independently.


What ICON Offers:

  • Competitive salary and comprehensive benefits.

  • Health insurance options for individuals and families.

  • Retirement planning and financial support services.

  • Global Employee Assistance Programme (LifeWorks).

  • Life assurance and flexible country-specific benefits.

  • Work-life balance programs and wellness support.

  • A diverse and inclusive work culture.


ICON is an Equal Opportunity Employer committed to creating an inclusive and accessible environment. Applicants with disabilities may request reasonable accommodations during the application process.