Senior Safety Lead, Global Clinical Trials (Remote)

Rho; España; Remote; EUR 70,000 - 100,000; Full time

Job summary

Rho is seeking a Senior Safety Specialist for remote work across Poland, the UK, or Spain. You will lead safety strategy, oversee end-to-end safety case processing, and collaborate with sponsors and internal teams to ensure compliance with protocols and SOPs.

Ideal candidates combine clinical safety expertise with strong communication skills and hands-on experience in pharmacovigilance, risk assessment, and regulatory requirements.

Qualifications

• Bachelor’s degree or equivalent with 5+ years of product safety/pharmacovigilance experience.
• 2 years as Product Safety Lead on Clinical Trials; develop Safety Management Plans and training materials.
• Experience with safety data collection, regulatory knowledge, and MedDRA/WHO Drug coding.
• Strong communication and presentation skills in English and local language.

Responsibilities

• Serve as primary Product Safety Lead for studies of moderate to high complexity.
• Lead study-level safety governance, data collection, processing and reporting activities.
• Develop and maintain study-specific Safety Management Plans and related documents.
• Act as primary Product Safety contact for sponsors and teams; manage communications.
• Chair safety meetings, prepare content, track decisions and actions.
• Oversee safety scope, timelines, budgets, and risk escalation.
• Mentor junior safety team members and contribute to training content.

Skills

Project management

Communication

Team collaboration

Detail orientation

Risk assessment

English proficiency

Education

Bachelor’s degree in Health Sciences / RN / PharmD

Tools

Argus

Excel

Word

PowerPoint

Job description

Rho is seeking a Senior Safety Specialist for remote work across Poland, the UK, or Spain. You will lead safety strategy, oversee end-to-end safety case processing, and collaborate with sponsors and internal teams to ensure compliance with protocols and SOPs.

Ideal candidates combine clinical safety expertise with strong communication skills and hands-on experience in pharmacovigilance, risk assessment, and regulatory requirements.