
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.
🕒 Yesterday
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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.
• Ensure that projects are delivered on time, within budget, and agreed scope, maintaining the appropriate industry, sponsor and Ergomed quality standards • Liaise with project team members, provide training where needed and ensure correct allocation to tasks • Develop, review and edit project plans to assure consistency with goals and milestones • Organization and facilitation of project meetings related to study activities (study organization, initiation, execution, closure) • Serve as primary point of contact with sponsor and Ergomed Senior Management on project status • Represent Ergomed at external meetings, providing liaison with scientific/medical experts in other CRO/Sponsor companies and for committee meetings, (e.g.EC/IRB) • Develop review and edit of relevant SOPs to assure consistency with Regulatory standards and develop study related training programs to support this. • Contribute to bid defense activities
• Experience serving as a Project Manager of international clinical trials in a CRO environment • Knowledge of Oncology and Rare Disease therapeutic areas • Experience in selecting and managing external service providers • Strong analytical, organizational and communication skills • Bachelor’s Degree in a science related discipline.
• flexible work arrangements • professional development
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