Remote Senior Product Safety Lead – Clinical Trials (Europe)

Rho

Polska

Hybrid

PLN 180,000 - 300,000

Full time

4 days ago
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Job summary

Rho is redefining what it means to work for a CRO. A Senior Safety Specialist role is open to candidates located in Poland, the UK, or Spain, with remote work options.

You will support federally and commercially funded clinical studies, ensuring adherence to protocols and SOPs while managing day-to-day safety activities and end-to-end case processing. The role involves leading study-level safety governance, developing Safety Management Plans, coordinating with sponsors and internal teams, and

Qualifications

  • Bachelor’s degree or equivalent plus 5+ years in product safety/pharmacovigilance.
  • 2 years as Product Safety Lead on Clinical Trials with Safety Management Plans.
  • Knowledge of pharmacovigilance regulatory requirements and safety databases.

Responsibilities

  • Serve as primary Product Safety Lead for studies of moderate to high complexity.
  • Lead safety governance, plan and oversee data collection, processing and reporting.
  • Develop and maintain Safety Management Plans aligned with protocols and sponsor expectations.
  • Act as primary Product Safety contact for sponsors and internal teams.
  • Chair safety meetings, document decisions and track actions to completion.
  • Manage safety scope, timelines and budgets; identify and escalate risks.
  • Provide guidance to Safety Specialists and Assistants; review deliverables.
  • Support study risk assessments and contribute to training of junior members.

Skills

Argus experience
Safety data reporting
Office software (Excel, Word, PowerPt)
Team collaboration
English proficiency

Education

Bachelor's degree in Health Sciences/Pharmacy/Nurse

Tools

Argus
Excel
Word
PowerPoint

Job description

Rho is redefining what it means to work for a CRO. A Senior Safety Specialist role is open to candidates located in Poland, the UK, or Spain, with remote work options.

You will support federally and commercially funded clinical studies, ensuring adherence to protocols and SOPs while managing day-to-day safety activities and end-to-end case processing. The role involves leading study-level safety governance, developing Safety Management Plans, coordinating with sponsors and internal teams, and

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