For over 85 years, Baxter has been at the forefront of medical innovation, impacting millions of lives worldwide. From life-saving products in hospitals to essential homecare solutions, Baxter’s mission is to save and sustain lives. As part of the organization, employees experience a meaningful purpose in their work and contribute to groundbreaking healthcare advancements. Baxter’s commitment to people goes beyond patients—it’s a place where professionals thrive, find purpose, and inspire one another to deliver the best outcomes.
Responsibilities in the Pharmacovigilance Job
As a member of Baxter’s Global Patient Safety (GPS) team, the Pharmacovigilance Specialist plays a critical role in ensuring the accuracy and timeliness of adverse event (AE) reporting. Key responsibilities include:
- Adverse Event Reporting: Processing adverse event reports from various sources and entering them accurately in the safety system.
- Data Management & Coding: Using medical knowledge to ensure correct drug selection and coding medical terms using standardized dictionaries like MedDRA.
- Causality Assessment: Determining seriousness, expectedness, and causality of adverse events reported by healthcare providers.
- Case Investigations: Collaborating with local affiliates to request additional information and generate follow-ups.
- Quality Assurance: Performing quality checks to ensure accuracy, consistency, and completeness of data for aggregate reports.
- Compliance with Deadlines: Handling tasks with efficiency under strict deadlines and managing changing priorities effectively.
Qualifications for Pharmacovigilance Specialist Role
To succeed in this role, you will need a combination of technical knowledge, communication skills, and the ability to adapt to a fast-paced work environment. The essential qualifications include:
- Medical and Clinical Knowledge: Understanding of medical terminology and patient safety principles.
- Communication Skills: Strong verbal and written communication abilities.
- Attention to Detail: Ability to accurately document and code complex medical data.
- Teamwork and Collaboration: Ability to work effectively in a team-based setting.
- Deadline Management: Comfort with multitasking, prioritizing, and working under strict timelines with minimal supervision.
Skills Required for Success
- Expertise in Pharmacovigilance Safety Systems
- Proficiency with MedDRA Coding
- Problem-solving abilities for case investigations and adverse event tracking
- Adaptability to shifting priorities and new challenges
- High level of organization and time management
