Hybrid Pharmacovigilance Trainee — Drug Safety

Esteve; Barcelona; Hybrid; EUR 42,000 - 60,000; Full time

Job summary

Grifols seeks a Technical Drug Safety Officer to join our international team. You will participate in safety data collection, review and compilation, and manage adverse event reports within regulatory timelines.

You will provide pharmacovigilance oversight for clinical studies and contribute to safety plans and reporting, ensuring compliance across departments. The role requires a health sciences degree and at least 1 year in a CRO or pharmaceutical setting, with fluency in Spanish and English.

Qualifications

• Bachelor's degree in health sciences (pharmacy, nursing, medicine, veterinary) or bioscience or similar.
• 1 year's experience in a similar position in a CRO or a pharmaceutical company.
• Fluent in Spanish and English.

Responsibilities

• Participate in safety data collection, review, processing, evaluation and compilation.
• Process adverse event case reports (mainly Serious Adverse Events) and ensure regulatory timelines.
• Provide pharmacovigilance oversight for clinical studies and act as Subject Matter Expert for clinical study documents.
• Contribute to safety management plans, SAE design, training and data reconciliation.
• Prepare DSURs, PSURs and Risk Management Plans and support inspections and audits.

Skills

Attention to detail

Excellent communication

Team player

Education

Bachelor's degree in health sciences or bioscience

Job description

Grifols seeks a Technical Drug Safety Officer to join our international team. You will participate in safety data collection, review and compilation, and manage adverse event reports within regulatory timelines.

You will provide pharmacovigilance oversight for clinical studies and contribute to safety plans and reporting, ensuring compliance across departments. The role requires a health sciences degree and at least 1 year in a CRO or pharmaceutical setting, with fluency in Spanish and English.