Ergomed careers
105 open roles at Ergomed (Pharma & Biotech) in Icsr Management, Clinical Monitoring, Patient Centricity. Read from its own careers site. Search and filter these.
Our products include the Medical Tube Securing line and Ventilator Anti-Disconnect Device. These unique products are used in Anesthesia, Respiratory Therapy, ICU, Emergency, Surgery, and more. ergomed.com
- IT Project Manager
- Senior Clinical Research Associate (West Coast based)
- Senior Clinical Research Associate (West Coast based)
- Senior Clinical Research Associate (West Coast based)
- Senior Auditor, Quality Assurance
- Senior Clinical Research Associate (East Coast based)
- Senior Clinical Research Associate (East Coast based)
- Senior Clinical Research Associate (East Coast based)
- Senior Auditor, Quality Assurance
- Senior Auditor, Quality Assurance
- Senior Clinical Research Associate - contractor (0.5 FTE)
- Senior System/Cloud Engineer
- CRA II
- Senior System/Cloud Engineer (Immediate Joiners preferred)
- Senior Principal Consultant
- Senior System/Cloud Engineer
- Senior System/Cloud Engineer
- Vendor Management Contracts Associate
- Business Development Director (Clinical Research), UK and Nordics
- Business Development Manager
- Business Development Manager
- Business Development Manager
- CRA Line Manager
- Medical Writer III (Pharmacovigilance)
- Medical Writer III (Pharmacovigilance)
- Business Development Director (Clinical Research), UK and Nordics
- Medical Writer III (Pharmacovigilance)
- Vendor Management Administrator - Student role
- Director, Business and Process Optimization (Pharmacovigilance)
- Director, Business and Process Optimization (Pharmacovigilance)
- Director, Business and Process Optimization (Pharmacovigilance)
- Study Start Up and Regulatory Affairs Specialist
- Case Processing Manager, Team Lead (PV Manager)
- Study Start Up and Regulatory Affairs Specialist
- Qualified Person Responsible for Pharmacovigilance (QPPV) in the EU and UK (homebased)
- Study Start Up and Regulatory Affairs Specialist
- Case Processing Manager, Team Lead (PV Manager)
- Qualified Person Responsible for Pharmacovigilance (QPPV) in the EU and UK (homebased)
- Qualified Person Responsible for Pharmacovigilance (QPPV) in the EU and UK (homebased)
- Copy of Qualified Person Responsible for Pharmacovigilance (QPPV) in the EU and UK (homebased)
- Senior Benefit/Risk Associate
- Trial Master File Specialist (TMFS) II - TMF and ALCOA principles experience required
- Trial Master File Specialist (TMFS) II - TMF and ALCOA principles experience required
- Specialist, Local Regulatory and PV network
- Trial Master File Specialist (TMFS) II - TMF and ALCOA principles experience required
- Local Contact Person for Pharmacovigilance and Regulatory Affairs (Contractor)
- Operations Manager (PV Technology)
- Clinical Research Associate II / Senior CRA (Spanish, Portuguese & English fluency)
- Local Contact Person for Pharmacovigilance and Regulatory Affairs (Permanent or Contractor)
- Clinical Research Associate II / Senior CRA (Spanish, Portuguese & English fluency)