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1–2 jobs· newest first

Safety Monitor EuropeNew
Emmes Group · Prague, Czech Republic+1 more
Senior Safety Specialist
Rho Inc · Remote, Poland+2 more
Remote · Full-time · Senior

+10K new in the last hour

Safety Monitor Europe

Emmes Group · Posted Nov 10, 2026

Prague, Prague, Czech Republic +1 more
4–6 years

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Responsible for safety monitoring and pharmacovigilance activities across interventional and non‑interventional clinical projects in Europe.

Locations (2)

Prague, Prague, Czech Republic
Slovakia

Responsibilities

Perform safety monitoring activities with project Medical Monitor or Medical Officer
Review safety events and adverse drug reaction cases
Provide first‑line evaluation of serious adverse events
Communicate with site staff regarding reported AEs or SAEs
Prepare summary narratives for DSMB reports and regulatory submissions

Requirements

Bachelor's Degree in Pharmacology, Medicine or Natural Science
Nice to have: 1-3 years experience in clinical practice
Nice to have: Experience in pharmacovigilance

Skills

Pharmacovigilance Medical Monitoring Good Pharmacovigilance Practice GxP MedDRA WHO drug coding

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Senior Safety Specialist

Rho Inc · Posted Nov 6, 2026

Remote, Poland +2 more
Remote
Full-time · Senior
5+ years

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Lead product safety activities for clinical studies, ensuring compliance with protocols and regulatory requirements.

Locations (3)

Poland
United Kingdom
Spain

Responsibilities

Serve as primary Product Safety Lead for assigned studies
Lead study-level safety governance and oversight
Develop and maintain Safety Management Plans
Act as primary contact for sponsors and internal teams
Chair or lead safety meetings

Requirements

Bachelor’s degree (e.g., RN, Health Sciences, PharmD) or equivalent
Nice to have: Experience with Argus

Skills

pharmacovigilance

safety database applications

WHO Drug coding

clinical trials

safety data collection

safety data processing

safety data reporting

global regulatory requirements

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