Clinical Trial Safety Scientist (Pharmacovigilance)

Location: Madrid, Spain; permanent home-based role

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Review ongoing patient-level clinical and safety data for medical accuracy, completeness, coding consistency, and case closure.
• Generate queries and escalate urgent or critical medical cases to study physicians or medical scientists.
• Prepare aggregated safety-data visualizations and facilitate study-level review meetings.
• Support study start-up activities, including document input and tool setup.
• Work with study physicians, clinical scientists, and project scientists on standardized data review and medical evaluation.
• Contribute to patient-narrative processes, training, continuous improvement, and procedure development.

Requirements

• Degree in Life Science or equivalent directly related experience.
• At least 2 years of experience in pharmacovigilance or drug safety.
• Understanding of clinical studies, drug development, ICH/GCP guidelines, and SAE reporting requirements.
• Strong analytical, prioritization, time-management, and communication skills.
• Ability to summarize complex information and manage multiple conflicting deadlines.
• Ability to work independently and cross-functionally with internal and external partners on global studies.

Nice to have

• Experience using data-review tools.

Culture & Benefits

• Permanent home-based work arrangement.
• Work across different phases of drug development and therapy areas.
• Collaboration with global study teams and external partners.
• Focus on integrity, diversity, inclusion, belonging, and equality.