Global Safety Scientist

BioTalent; Brussel; On-site; EUR 60,000 - 90,000; Full time

Job summary

BioTalent is collaborating with a leading biopharma company to support Global product safety across clinical and post market assets. We are seeking a Pharmacovigilance professional to contribute to signal detection, risk assessment, and safety governance.

The role involves preparing key PV deliverables, supporting regulatory submissions, and collaborating with cross-functional teams to ensure global PV compliance. A Life Sciences or related degree and 3+ years PV experience are required.

Qualifications

• 3+ years experience in Pharmacovigilance (PV) including clinical and post-marketing settings.
• Strong knowledge of global PV regulations, safety science and benefit-risk assessment.
• Excellent communication and stakeholder management skills.
• Proactive, collaborative and delivery-focused with ability to manage competing priorities.

Responsibilities

• Support signal detection, benefit-risk evaluation, safety surveillance and risk management activities.
• Contribute to multidisciplinary safety governance teams and clinical development programs.
• Prepare and maintain PV deliverables such as PSURs, DSURs and Risk Management Plans.
• Support regulatory submissions, health authority interactions and post-marketing safety activities.
• Collaborate with cross-functional stakeholders to ensure compliance with global PV requirements.

Skills

PV experience

Regulatory knowledge

Stakeholder management

Analytical thinking

Education

Life Sciences/Pharmacy/Healthcare degree

Job description

BioTalent is collaborating with a leading biopharma company to support Global product safety across clinical and post market assets.

Key Responsibilities

• Support signal detection, benefit-risk evaluation, safety surveillance, and risk management activities.
• Contribute to multidisciplinary safety governance teams and clinical development programs.
• Prepare and maintain key pharmacovigilance deliverables including PSURs, DSURs and Risk Management Plans.
• Support regulatory submissions, health authority interactions, post-marketing safety activities and safety-related scientific communications.
• Collaborate with cross-functional stakeholders to ensure compliance with global pharmacovigilance requirements.

Requirements

• Degree in Life Sciences, Pharmacy, Healthcare, or a related discipline.
• 3+ years experience in PV, Drug Safety (in both clinical and post marketing setting)
• Strong knowledge of Global PV regulations, safety science and benefit-risk assessment.
• Strong analytical thinking, communication, stakeholder management and problem-solving skills.
• Proactive, collaborative, and delivery-focused mindset with the ability to manage competing priorities.