
1001 - 5000 employees
Founded 1997
💼 Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
🔥 14 minutes ago
Where this job comes from
Posted on ERGOMED's careers page, not through a job board
First seen by Remote Rocketship 14 minutes ago
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1001 - 5000 employees
Founded 1997
💼 Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
• Manage and conduct internal and contracted audits for the Company and its Clients • Provide input into audit strategy and risk-based audit planning • Lead process and complex audits • Provide QA consultancy within area of GxP expertise • Conduct audits of partners, vendors/service providers, internal systems, study files, investigational sites, and third parties • Manage pre-audit activities • Review and approve final CAPA plans within required timelines • Perform client PV/QMS system gap analyses and SOP development • Serve as main QA contact for designated Clients • Plan, conduct, and report on audits requested by Clients • Attend commercial meetings related to Quality as a Service • Support clients with mock inspections, training, gap analysis, and procedure drafting/revision • Support audits and inspections performed by Clients, third parties, and regulatory authorities • Develop and train Auditors and other quality employees • Assist in developing the strategic internal audit program • Maintain current knowledge of international regulatory requirements, guidelines, and best practices • Participate in authoring or quality control of audit strategies, SOPs, guidelines, and other procedures
• Bachelor’s degree in a scientific discipline required; Master’s degree preferred, or equivalent relevant industry experience • Strong previous pharmaceutical and/or biotech pharmacovigilance experience • Strong understanding of GVP and GCP related Quality Management and Assurance • Previous GVP and GCP auditing experience in an Audit Lead role • Analytical, written and oral communication skills • Ability to manage assigned tasks and deliver expected deliverables in an organized and timely manner • Ability to proactively communicate changes in pre-established goals and deadlines • Ability to think strategically and work collaboratively using risk-based, proactive approaches to problem-solving • Strong team player • Fluent in English, written and spoken • Additional/local languages are a plus but not required
• Remote work available • Collaborative team environment • Opportunities for growth and professional development • Knowledge-sharing and learning opportunities • Training opportunities • Diverse and inclusive workplace • Opportunity to make a difference to patients’ lives
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