IQVIA is at the forefront of the healthcare and life sciences industries, providing cutting-edge solutions that accelerate the development and commercialization of medical treatments. With a global presence, IQVIA leverages data, technology, and advanced analytics to improve patient outcomes and transform healthcare worldwide.
Job Responsibilities
As a Safety Associate at IQVIA, you will:
- Case Processing
- Manage safety cases in the Japanese language.
- Ensure timely and accurate data entry into safety databases.
- Compliance
- Adhere to regulatory guidelines, standard operating procedures (SOPs), and client requirements.
- Collaboration
- Work closely with cross-functional teams to ensure smooth workflow and compliance with safety protocols.
- Quality Assurance
- Perform quality checks to ensure the accuracy and completeness of processed cases.
- Reporting
- Generate and review safety reports, ensuring all necessary details are included.
Qualifications
To qualify for this role, you must have:
- A degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Proficiency in the Japanese language (reading, writing, and speaking).
- Prior experience in pharmacovigilance or a similar role (preferred but not mandatory).
Required Skills
- Language Proficiency: Fluency in Japanese is a must.
- Attention to Detail: Ability to manage and review case data accurately.
- Communication Skills: Strong verbal and written communication skills.
- Time Management: Capable of prioritizing tasks to meet tight deadlines.
- Technical Knowledge: Familiarity with safety databases and pharmacovigilance processes is an advantage.
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