Remote Jobs at ERGOMED
Find your next remote opportunity · 28 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
Talent Acquisition Specialist
Talent Acquisition Specialist recruiting pharmacovigilance, clinical research, and corporate professionals for Ergomed’s pharmaceutical services. Managing sourcing, screening, interviews, offers, and talent pipelines across Europe.
Senior Specialist, Study Start Up – Regulatory Affairs
Senior study start-up specialist leading regulatory readiness for Ergomed’s rare disease and oncology clinical trials. Coordinating submissions, site agreements and activation across assigned countries.
Senior Benefit/Risk Associate
Senior Benefit/Risk Associate conducting pharmacovigilance signal detection and risk evaluation for PrimeVigilance. Supporting regulatory communications and patient-safety activities within global project teams.
Manager, Regulatory Registration and Compliance
Regulatory compliance manager leading pharmaceutical submissions and complex regulatory projects at PrimeVigilance. Guiding clients and teams across global pharmacovigilance and patient-safety programs.
Local Contact Person – Pharmacovigilance, Regulatory Affairs
Local pharmacovigilance and regulatory affairs specialist supporting pharmaceutical compliance and patient safety. Managing ADR reporting, regulatory submissions, local requirements, and MAH relationships.
Local Contact Person – Pharmacovigilance and Regulatory Affairs
Local pharmacovigilance and regulatory affairs specialist supporting PrimeVigilance’s pharmaceutical clients. Managing ADR reporting, regulatory submissions, compliance, audits, and local safety requirements.
Talent Acquisition Specialist, Full Time Student Position
Talent Acquisition Specialist recruiting clinical and pharmaceutical professionals for Ergomed’s life-science services. Managing sourcing, screening, interviews, offers and talent pipelines across regions.
Project Manager, Oncology Experience
Project Manager leading international oncology and rare disease clinical trials for Ergomed, a specialist clinical research organization. Managing timelines, budgets, sponsors, teams, and regulatory-quality deliverables.
Medical Information Associate, Dutch
Medical Information Associate handling Dutch and English medical inquiries and adverse-event reporting. Supporting PrimeVigilance’s global pharmacovigilance services that protect pharmaceutical patients.
Medical Information Associate, Dutch Language
Medical Information Associate handling Dutch and English medical inquiries for PrimeVigilance, a global pharmacovigilance specialist. Documenting adverse events and supporting regulatory inspections to protect patient safety.
Medical Information Associate – Dutch
Medical Information Associate supporting PrimeVigilance’s global pharmacovigilance services through Dutch and English medical inquiry handling. Documenting adverse events and supporting regulatory inspections.
Senior Site Contracts Specialist
Senior Site Contracts Specialist negotiating clinical trial agreements for Ergomed’s rare disease and oncology clinical research. Supporting biotech sponsors and study teams across U.S. hiring locations.
Global HR Business Partner – CRO, Life Science Experience
Global HR Business Partner shaping workforce, talent, and culture strategy for Ergomed’s global pharmacovigilance operations. Advising senior leaders supporting safer pharmaceutical therapies.
Global HR Business Partner – CRO, Life Science Experience Required
Global HR Business Partner shaping workforce strategy for Ergomed’s global pharmacovigilance teams. Advising senior leaders across countries on talent, culture, change, compensation, and compliance.
Global HR Business Partner – CRO, Life Science Experience Required
Global HR Business Partner shaping workforce, talent, culture, and change strategy for Ergomed’s global pharmacovigilance teams. Supporting pharmaceutical and clinical research operations across countries.
Global HR Business Partner – CRO, Life Science Experience Required
Global HR Business Partner shaping people strategy for Ergomed’s pharmacovigilance teams. Advising senior leaders across countries to build talent, culture, and capability supporting global drug safety.
Proposals Manager – Pharmacovigilance
Proposals Manager leading development of proposals in Pharmacovigilance at PrimeVigilance. Collaborating with stakeholders and ensuring high quality client-focused proposals.
Proposals Manager – Pharmacovigilance
Proposals Manager in Pharmacovigilance handling proposal development and client engagement. Join a collaborative team dedicated to patient safety and regulatory navigation.
Proposals Manager – Pharmacovigilance
Proposals Manager developing and managing proposals for pharmacovigilance at PrimeVigilance. Leading the proposal development process within the Clinical Research Organization industry.
Proposals Manager – Pharmacovigilance
Proposals Manager leading proposal development and ensuring client satisfaction in the CRO environment. Collaborating with stakeholders to create high-quality proposals for new business opportunities.