Remote Jobs at ERGOMED
Find your next remote opportunity · 16 Open Positions
Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information.
Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology.
• 1,800+ highly qualified professionals
• Global full-service CRO
• 25+ years of experience
• Therapeutic specialization in oncology
• Strong expertise in rare disease trials
• Robust clinical safety system
• Choice of leading drug safety databases
Our key services include:
• Clinical Research Services
• Pharmacovigilance
• Medical Information
• Regulatory
• Medical Writing
• Site Management
• Study Physician Support
• Biostatistics
• Patient Study Support
Clinical Research Associate II
Clinical Research Associate II overseeing monitoring visit activities for clinical studies. Working with investigational sites to ensure qualifications and resources are adequate throughout the trials.
Global Human Resources Business Partner
Global HR Business Partner responsible for driving HR strategies and initiatives. Collaborating with leaders to meet global business objectives.
Benefit/Risk Officer
Benefit/Risk Officer supporting pharmacovigilance activities for PrimeVigilance. Requires life science background with signal detection experience and strong communication skills.
Benefit/Risk Officer
Benefit/Risk Officer supporting pharmacovigilance activities including signal detection and regulatory communication at PrimeVigilance. Requires life science background and experience in signal management tools.
Benefit/Risk Officer
Benefit/Risk Officer at PrimeVigilance contributing to pharmacovigilance activities and learning in a global setting. Engaging in signal detection and collaborating with various company departments.
Senior Pharmacovigilance Manager – PV Systems
PV Manager leading safety database oversight, ensuring data quality and regulatory compliance in pharmacovigilance service. Driving continuous improvement and team mentorship across global teams.
Contact Center Administrator
Contact Center Administrator managing contact center systems for PrimeVigilance, a global pharmacovigilance provider. Responsible for ensuring system performance and providing agent support in a dynamic environment.
Associate Senior Pharmacovigilance Manager – PV Systems
PV Manager in pharmacovigilance ensuring data quality and regulatory compliance. Collaborating across teams to drive continuous improvement and mentor junior members.
Senior Pharmacovigilance Manager – PV Systems
Lead Pharmacovigilance Manager ensuring data quality and system optimization at PrimeVigilance. Oversee database design and validation while mentoring junior team members for excellence in safety systems.
Medical Writer III
Medical Writer at PrimeVigilance responsible for developing regulatory documents related to drug safety. Join a global team enhancing patient safety through quality medical writing.
Senior Medical Writer – Line Management Experience Required
Senior Medical Writer developing various regulatory and clinical documents for drug safety. Joining PrimeVigilance in making a positive impact in patient lives with a focus on professional growth.
No more jobs available.