IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services to the life sciences and healthcare industries. With a mission to drive healthcare forward, IQVIA creates intelligent connections between data, technology, and expertise. As part of its global operations, IQVIA accelerates the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
Job Responsibilities
As an Operations Specialist 1 in Lifecycle Safety at IQVIA, your primary role will be to review, assess, and process safety data and reports across various service lines. Working under the guidance of senior team members, your responsibilities will include:
- Prioritizing Training: Complete all assigned training modules on time.
- Safety Data Management: Process safety data and adverse event reports following regulations, guidelines, and standard operating procedures (SOPs).
- Pharmacovigilance Activities: Collect, track, and assess adverse event (AE) or endpoint information, determine status updates, code AEs and products, and write case narratives.
- Database Management: Enter and maintain data within the applicable safety database.
- Quality Compliance: Meet productivity, quality, and delivery standards in line with project requirements.
- Collaboration: Work with cross-functional teams, including project management, clinical data management, and healthcare professionals, to address project-related issues.
- Mentorship: Mentor new team members and support department initiatives when assigned.
In addition, you may perform medical reviews of non-serious adverse events (AEs) and adverse drug reactions (ADRs) based on project requirements. You will also need to attend project team meetings and provide feedback to the operations manager.
Qualifications
To be considered for the Operations Specialist 1 role at IQVIA, you need the following qualifications:
- Bachelor’s degree in Life Sciences or a related field.
- 3-5 years of experience in Pharmacovigilance.
- Knowledge of medical terminology and Pharmacovigilance (PV) concepts.
- Familiarity with safety databases and client applications.
- Awareness of global, regional, and local clinical research regulations.
- Strong organizational and time management skills.
- Proficiency in Microsoft Office and web-based applications.
Skills Required
The role requires strong attention to detail, accuracy, and the ability to maintain high-quality standards. Additionally, candidates should demonstrate:
- Communication: Strong verbal and written communication skills.
- Multitasking: Ability to manage multiple tasks, meet deadlines, and prioritize work in a dynamic environment.
- Teamwork: Ability to work effectively within a team and foster productive working relationships with coworkers, clients, and managers.
- Flexibility: Willingness to learn new skills, adapt to changing processes, and work shifts as needed.
