IQVIA, a premier global provider of clinical research services and healthcare intelligence, is seeking a Pharmacovigilance Specialist fluent in English, Spanish, and French for a full-time, home-based position in Mexico City, Mexico (Job ID: R1479248). This trilingual role offers an exciting opportunity to contribute to patient safety by processing and analyzing safety data for innovative medical treatments, supporting IQVIA’s mission to improve health outcomes worldwide.
Job Details
- Position: Pharmacovigilance Specialist
- Location: Mexico City, Mexico (100% home-based; additional locations may be available)
- Employment Type: Full-time
- Job ID: R1479248
- Application Deadline: Not specified; apply promptly
- Application Method: Apply online at https://jobs.iqvia.com or email CV to recruitment@iqvia.com
Role Overview
As a Pharmacovigilance Specialist, you will review, assess, and process safety data from various sources under the guidance of senior team members. This role involves ensuring compliance with global regulations, Standard Operating Procedures (SOPs), and project-specific guidelines while collaborating with internal teams and healthcare professionals.
Main Responsibilities
Safety Data Processing:
- Collect, track, and process Adverse Events (AEs) and endpoint information per applicable regulations and SOPs.
- Determine initial/update status of incoming events, perform database entry, and code AEs and products.
- Write case narratives and conduct literature-related pharmacovigilance activities.
Medical Review (if required):
- Perform medical review of non-serious AEs and Adverse Drug Reactions (ADRs), including coding, causality assessment, and expectedness/listedness evaluation.
- Ensure completeness and accuracy of medical data and maintain documentation for all communications.
Compliance and Quality:
- Adhere to quality, productivity, and delivery standards per project requirements.
- Read, acknowledge, and comply with IQVIA and client SOPs.
- Complete assigned trainings on time and maintain an updated training transcript.
Collaboration:
- Liaise with functional teams (e.g., project management, clinical, data management) and healthcare professionals (e.g., investigators, medical monitors) to address project issues.
- Mentor new team members as assigned by the manager.
Additional Duties:
- Support client interactions for day-to-day case processing activities.
- Lead or contribute to departmental initiatives as needed.
Qualifications
- Education: Bachelor’s degree in Life Sciences or a related field (mandatory)
- Language Skills: Fluency in English, Spanish, and French (mandatory)
Experience:
- 1 year of pharmacovigilance experience is highly valued but not mandatory.
- Familiarity with safety data processing or clinical research is an advantage.
Technical Skills:
- Good working knowledge of Microsoft Office (Word, Excel, Outlook) and web-based applications.
- Intermediate proficiency in database systems or pharmacovigilance software is preferred.
Soft Skills:
- Strong attention to detail, organizational skills, and ability to work remotely.
- Effective communication and collaboration skills in a multicultural environment.
Documents to Prepare
When applying, ensure you have:
- Updated CV (mention Job ID: R1479248 and “Pharmacovigilance Specialist” in the email subject if applying via email)
- Copies of educational certificates (Bachelor’s degree in Life Sciences or related field)
- Language proficiency certificates or proof (if available, for English, Spanish, and French)
- Experience certificates (if applicable, especially for pharmacovigilance roles)
- Aadhar Card, PAN Card, or equivalent ID copies (as per local requirements)
Why Join IQVIA?
- Global Impact: Contribute to a company accelerating the development of innovative medical treatments, impacting patient outcomes in 100+ countries.
- Flexible Work: Enjoy a 100% home-based role, offering work-life balance with a 4.3/5 employee rating for flexibility (Glassdoor data).
- Career Growth: Access continuous learning through IQVIA’s training programs, with 78% of employees recommending it for professional development.
- Industry Leadership: Work with a Fortune 500 company partnering with top pharmaceutical and biotech firms, leveraging advanced analytics and AI-driven solutions.
How to Apply
Interested candidates fluent in English, Spanish, and French are encouraged to:
- Apply directly at https://jobs.iqvia.com using Job ID: R1479248.
- Alternatively, email their CV and supporting documents to recruitment@iqvia.com with the subject “Pharmacovigilance Specialist – R1479248”.
Verified by Trusted HRs
The post is released by the IQVIA LinkedIn page. Click here to visit the post
Join IQVIA and advance your career in pharmacovigilance while contributing to global healthcare innovation! We look forward to welcoming you to our team in Mexico City or other eligible locations.