Job Description

Support the processing, assessment, and distribution of Safety data across multiple service lines. Handle information received from various sources and ensure timely reporting to internal and external stakeholders, following regulations, SOPs, and internal guidelines under the supervision of senior team members.

Essential Functions

• Complete assigned training requirements within established timelines.
• Process Safety data in accordance with regulations, guidelines, SOPs, and project specifications.
• Perform Pharmacovigilance activities, including collecting and tracking Adverse Events (AEs) and endpoint information.
• Determine initial and follow‑up status of reported events.
• Enter data into Safety databases, code AEs and products, and prepare narratives.
• Support literature‑related activities as required by project timelines.
• Meet project‑specific quality, productivity, and delivery standards.
• Maintain compliance with all project processes and documentation requirements.
• Create, update, and track case information according to project plans.
• Identify and escalate quality issues to senior team members.
• Demonstrate problem‑solving skills and support new team members when assigned.
• Participate in project meetings and provide feedback on challenges or successes.
• Maintain 100% compliance with people processes and organizational practices.
• Perform additional duties as assigned.

Qualifications

• Bachelor’s degree in life sciences and 1–2 years of relevant experience required.
• Good knowledge of medical terminology
• Basic working knowledge of Safety databases and global/regional regulatory requirements.
• Strong attention to detail and accuracy.
• Proficiency with Microsoft Office and web‑based applications.
• Strong organizational and time‑management skills.
• Effective verbal and written communication skills.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.