We are looking for a Pharmacovigilance Technician to join our team and play a key role in ensuring the safety of marketed and investigational medicinal products. This position will provide pharmacovigilance services to one of our pharmaceutical clients, offering the opportunity to work in a highly specialized and international environment.
Key Responsibilities
• Manage adverse event reports from collection to evaluation, data entry, review, distribution, and archiving.
• Ensure timely reporting of safety cases to health authorities in accordance with company procedures and regulatory requirements.
• Conduct literature searches to identify potential adverse drug reactions.
• Prepare, review, and distribute safety reports, including IPS and DSUR submissions.
• Deliver pharmacovigilance training to internal stakeholders.
• Maintain and ensure the quality of the pharmacovigilance database.
• Manage SAE and SUSAR cases related to clinical trials, including database entry and causality assessment.
• Support additional pharmacovigilance activities and new project initiatives as required.
Essential Requirements
• Degree in Pharmacy, Biology, Life Sciences, or a related Healthcare discipline.
• Minimum 1 year of experience in Pharmacovigilance.
• Master's Degree or Postgraduate qualification in the Pharmaceutical Industry will be considered an advantage.
• High level of English.
• Dynamic, proactive, and organized professional with strong communication and leadership skills.
• Ability to work effectively in a collaborative and fast-paced environment.
What we offer
• Attractive compensation package.
• Adaptable working hours.
• Hybrid working model with teleworking options.
• Professional development and continuous learning opportunities.
• A collaborative environment where innovation, growth, and talent are highly valued.
Location & Working Model
Barcelona, Spain | Hybrid
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