Remote Jobs at ERGOMED

Senior Specialist, Regulatory & PV Network

Senior Specialist managing regulatory and pharmacovigilance deliverables at PrimeVigilance. Leading strategy development and acting as liaison with regulatory authorities and clients.

Legal Counsel

Legal Counsel at Ergomed Group, drafting and negotiating agreements across global clients in healthcare and regulatory fields. Collaborating on corporate governance and compliance with legal requirements.

Contact Center Administrator

Contact Center Administrator responsible for configuring and optimizing contact center systems at PrimeVigilance. Collaborating across teams to ensure efficient operations and excellent customer service.

Associate Director, Data Intelligence

Associate Director supporting data intelligence strategy focusing on Oncology and Rare Disease for PrimeVigilance. Engaging in global operational strategy and feasibility data analysis.

Associate Director, Data Intelligence

Senior Director/Director, Data Intelligence supporting operational strategy globally with a focus on Oncology and Rare Disease. Managing feasibility studies and data collection for clinical projects.

Associate Director, Data Intelligence

Associate Director of Data Intelligence supporting pre-award study feasibility strategy in Oncology and Rare Disease at PrimeVigilance, a pharmacovigilance service provider.

Senior Director/Director, Data Intelligence

Supports operational strategy globally in key therapeutic areas of Oncology and Rare Disease. Assists with feasibility analysis and proposal development for new business opportunities.

Senior Director/Director, Data Intelligence

Sr. Director/Director, Data Intelligence leading operational strategy through data analysis in pharmacovigilance. Collaborating on proposal development and market research in Oncology and Rare Disease.

Sr. Director/Director, Data Intelligence

Director of Data Intelligence at PrimeVigilance focusing on global operational strategy and data analysis for Rare Disease and Oncology. Assisting RFP processes and developing strategic feasibility packages.

Associate Director, Tax

Associate Director managing global tax strategy and compliance at Ergomed. Lead tax planning, compliance, and advisory functions across jurisdictions with a focus on UK and US tax.

Medical Reviewer I

Medical Reviewer managing pharmacovigilance assessments and safety reports for PrimeVigilance. Collaborating with cross-functional teams to ensure compliance and safety in clinical trials.

Medical Reviewer I

Medical Reviewer in Pharmacovigilance reviewing post-marketing safety reports and ensuring compliance. Collaborating internationally in a supportive work environment.

Proposals Manager

Proposals Manager leading development and strategy of client-focused proposals at Ergomed Clinical Research. Collaborating across departments to ensure high-quality outcomes for clinical trials.

Senior Client Quality Manager

Senior Client Quality Manager overseeing project compliance for pharmacovigilance services. Driving quality improvements and managing client quality activities in a supportive international environment.

Senior Client Quality Manager

Senior Client Quality Manager ensuring compliance and quality oversight for client projects at PrimeVigilance. Driving improvement initiatives and managing client relations within a global team.

Senior Client Quality Manager

Senior Client Quality Manager responsible for implementing quality systems in pharmacovigilance. Managing project quality activities and ensuring compliance with regulations in a global context.

Senior Client Quality Manager

Senior Client Quality Manager

Senior Client Quality Manager overseeing quality activities for client projects at PrimeVigilance. Ensuring compliance with global regulations while providing quality improvement advice and team support.

Medical Reviewer I

Medical Reviewer conducting post-marketing Individual Case Safety Reports for pharmacovigilance. Reviewing safety data and providing insights into clinical trials and adverse event reports.

Medical Reviewer I

Medical Reviewer responsible for reviewing post-marketing lCSRs and SAEs in clinical trials. Role involves literature review, database output review, and input in safety reports.