Clinical Data Reviewer
hace 4 días
We are looking for a highly motivated and organized Pharmacovigilance Specialist to join our team at IQVIA Argentina. As a critical member of our team, you will be responsible for managing safety data and information, working closely with senior team members to ensure compliance with regulatory requirements.
Key Responsibilities:
- Managing safety data according to regulatory requirements and project specifications.
- Performing pharmacovigilance activities, including data collection, tracking, and analysis.
- Collaborating with cross-functional teams and external partners to achieve project goals.
- Mentoring junior colleagues and contributing to departmental initiatives.
Requirements:
- Bachelor's degree in life sciences or a related field.
- Up to 3 years of relevant experience, including up to 1 year of pharmacovigilance experience.
- Fluency in English, Spanish, and French.
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