🕒 3 days ago
Lead IT infrastructure and cloud initiatives, shaping Azure and hybrid-cloud strategy while improving security, cost, reliability, and automation across enterprise systems and Microsoft 365.
Ergomed jobs
ERGOMED Group offers custom-made clinical solutions for every stage of development from proof-of-concept to late-stage programs.
👥 501 - 1000 employees🏢 Biotechnology🎯 Orphan Drugs🌍 United Kingdom🚩 Founded 1997💰 Funding: Post IPO Equity
113 open roles at Ergomed
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🕒 3 days ago
Perform and support pharmacovigilance signal management, from reviewing safety data and evaluating potential signals to drafting reports and supporting regulatory communications.
🕒 3 days ago
Author and quality-check pharmacovigilance and regulatory documents, interpret safety data with cross-functional teams, support client relationships, and mentor junior medical writers.
🕒 3 days ago
Serve as the local Regulatory Affairs and Pharmacovigilance representative, carrying out country-level safety and compliance activities, advising on regulatory requirements, and supporting product compliance throughout its lifecycle.
Trial Master File Specialist (TMFS) II - TMF and ALCOA principles experience required
🕒 4 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 4 days ago
Maintains Trial Master Files for assigned clinical research projects, overseeing document processing, indexing, quality checks, reporting, audit support, and study closeout in line with project guidelines and ALCOA+ principles.
Trial Master File Specialist (TMFS) II - TMF and ALCOA principles experience required
🕒 4 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 4 days ago
Maintains Trial Master Files for assigned clinical research projects, serving as the TMF contact and ensuring documents meet project guidelines, SOPs, quality standards, and ALCOA+ principles.
Trial Master File Specialist (TMFS) II - TMF and ALCOA principles experience required
🕒 4 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 4 days ago
Maintains Trial Master Files for assigned clinical research projects, overseeing document processing, indexing, quality checks, reporting, audit support, and study-closeout reconciliation and archiving.
Clinical Research Associate II / Senior CRA (Spanish, Portuguese & English fluency)
🕒 5 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 5 days ago
Conducts clinical trial monitoring across Spain and Portugal, assessing investigator and site readiness, training site staff, and supporting regulatory submissions for Phase 2/3 studies.
📍 🇵🇹 Portugal - Remote💼 Full-Time🎸 Senior🧫 Clinical Research Specialist📢 🇪🇸 Spanish Required📢 🇧🇷🇵🇹 Portuguese Required
Clinical Research Associate II / Senior CRA (Spanish, Portuguese & English fluency)
🕒 5 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 5 days ago
Conduct pre-study, initiation, interim, and close-out monitoring visits in Spain and Portugal, verifying site and investigator readiness, training staff, and supporting regulatory or ethics committee submissions.
📍 🇪🇸 Spain - Remote💼 Full-Time🎸 Senior🧫 Clinical Research Specialist📢 🇪🇸 Spanish Required📢 🇧🇷🇵🇹 Portuguese Required
Local Contact Person for Pharmacovigilance and Regulatory Affairs (Contractor)
🕒 6 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 6 days ago
Serve as Australia’s local pharmacovigilance and regulatory affairs contact, coordinating safety reporting, regulatory intelligence, compliance activities, and product documentation for the Marketing Authorisation Holder.
Local Contact Person for Pharmacovigilance and Regulatory Affairs (Contractor)
🕒 6 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 6 days ago
The Specialist, Local RA & PV Network ensures compliance with national pharmacovigilance and regulatory requirements, acting as the primary local representative for RA and PV activities.
Local Contact Person for Pharmacovigilance and Regulatory Affairs (Contractor)
🕒 6 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 6 days ago
The Specialist, Local RA & PV Network acts as the primary local representative for Pharmacovigilance and Regulatory Affairs, ensuring compliance with national regulations in Australia.
Local Contact Person for Pharmacovigilance and Regulatory Affairs (Permanent or Contractor)
🕒 6 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 6 days ago
The Specialist, Local RA & PV Network ensures compliance with national pharmacovigilance and regulatory requirements, acting as the primary local representative for RA and PV activities.
Local Contact Person for Pharmacovigilance and Regulatory Affairs (Permanent or Contractor)
🕒 6 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 6 days ago
The Specialist, Local RA & PV Network ensures compliance with national pharmacovigilance and regulatory requirements, acting as the primary local representative for RA and PV activities.
Local Contact Person for Pharmacovigilance and Regulatory Affairs (Contractor position)
🕒 6 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 6 days ago
The Local Contact Person for Pharmacovigilance and Regulatory Affairs will ensure compliance with national pharmacovigilance and regulatory requirements while supporting product lifecycle management.
🕒 7 days ago
Manage individual case safety reports and related pharmacovigilance activities, ensuring regulatory and client-specific compliance while supporting patient safety, reporting, and local safety processes.
🕒 7 days ago
Manage Individual Case Safety Reports (ICSRs) and related pharmacovigilance activities, ensuring regulatory and client requirements are met while supporting patient safety and timely safety-data reporting.
🕒 7 days ago
Provides technical expertise for pharmacovigilance systems, maintaining and configuring Argus Safety databases, supporting data migrations and integrations, and ensuring validated, compliant safety reporting.
🕒 9 days ago
The Data Engineer will design, build, and optimize data integration pipelines to enhance enterprise-wide analytics and ensure compliance with data governance standards.
Site Manager (clinical research, local site coordinator role)
🕒 10 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 10 days ago
The Site Manager facilitates clinical studies by providing patient-related site support, ensuring compliance with protocols, and optimizing site staff performance.
Site Manager (clinical research, local site coordinator role)
🕒 10 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 10 days ago
The Site Manager facilitates clinical studies by providing patient-related site support and ensuring compliance with protocols and regulatory requirements.
📍 🇩🇪 Frankfurt am Main - Remote💼 Full-Time🎹 Mid-level📋 Manager📢 🇬🇧 English Required📢 🇩🇪 German Required
Clinical Research Associate II / Senior CRA (French Speaking)
🕒 10 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 10 days ago
Conducts clinical trial monitoring visits and supports investigational sites through study start-up, ongoing oversight, and close-out, helping maintain site readiness and study quality in complex trials.
📍 🇪🇸 Spain - Remote💼 Full-Time🎸 Senior🧫 Clinical Research Specialist📢 🇫🇷 French Required📢 🇬🇧 English Required
Business Development Director (Clinical Research), UK and Nordics
🕒 10 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 10 days ago
The Business Development Director will lead strategic sales initiatives, develop account strategies, and identify new business opportunities within the clinical research sector.
Director, Clinical Vendor Strategy (North America) - previous clinical research experience required
🕒 10 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 10 days ago
The Director, Clinical Vendor Strategy is responsible for leading clinical outsourcing strategies and vendor governance to ensure successful clinical trial delivery.
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