ergomed

Ergomed Warsaw is seeking a Senior Benefit-Risk Associate to join a project team delivering contracted pharmacovigilance activities for PrimeVigilance. The role focuses on signal detection, risk assessment, and collaboration with regulatory bodies.You will review line listings, draft signal detection reports, evaluate signals, and maintain tracking tools,...

Ergomed Group, a leading CRO, seeks a Director of Clinical Vendor Strategy to drive outsourcing strategy and governance across the clinical development portfolio. You will partner with Clinical Operations, Vendor Management, Therapeutic Strategy, Regulatory, Quality, and Finance to optimize vendor selection and outsourcing models.Serving as a strategic...

Ergomed Group is seeking a Project Manager to lead IT projects from initiation through production, ensuring scope, timelines and budgets are met. You will coordinate stakeholders, manage 3rd parties, and oversee QA, validation, and handover to production environments.The role emphasizes governance, reporting, risk management, and budget oversight across IT...

Medicine moves forward here. So will you.Clinical trials, safety studies, and audits make safe and innovative pharmaceutical-led care possible. As part of Ergomed Group, you help patients benefit so they experience more of life’s meaningful moments. Biopharmaceutical companies are our clients. Patients are our purpose.Ergomed Group brings together Ergomed...

Ergomed is seeking a PV Auditor on a freelance basis to cover audits across Europe. The role involves planning, conducting, reporting and CAPA follow-up for pharmacovigilance audits in line with GVP requirements.Travel will be required in addition to remote audits, with both 0.6 FTE and full-time options being considered. You will apply expert knowledge of...

Ergomed Group is a global CRO focused on rare disease and oncology, seeking an experienced oncology strategy professional to coordinate competitive pre-award activities and drive opportunities across indications.You will lead bids, collaborate with global functions, and strengthen client relationships, contributing to high-quality trial delivery and patient...

Ergomed Group's PrimeVigilance unit is seeking a Senior Benefit-Risk Associate to join a global pharmacovigilance team. You will perform and support contracted PV activities for clients, focusing on signal detection, reporting, and regulatory communications.Ideal candidates will have life sciences background, experience in signal detection, and strong...

Ergomed is a specialist CRO focused on rare disease and oncology, collaborating with biotechs to accelerate early-phase development. The team emphasizes data-driven decision making, feasibility, and operational excellence across global sites.The role involves collecting, validating, and analyzing data from multiple sources to identify trends, generate...

Department: Strategy & Transformation Realization Office Company Description Medicine moves forward here. So will you. Clinical trials, safety studies, and audits make safe and innovative pharmaceutical-led care possible. As part of Ergomed Group, you help patients benefit so they experience more of life's meaningful moments. Biopharmaceutical companies are...

Company Description Medicine moves forward here. So will you. Clinical trials, safety studies, and audits make safe and innovative pharmaceutical-led care possible. As part of Ergomed Group, you help patients benefit so they experience more of life’s meaningful moments. Biopharmaceutical companies are our clients. Patients are our purpose. Ergomed Group...

Ergomed Group in Warszawa is seeking a full-time ICSR Management professional to lead a team and drive KPI-based performance within pharmacovigilance. You will oversee line management, QA, and cross‑functional support for clients and the company.The role requires a life science background, 5–6 years in pharmacovigilance with at least 3 years in a...

Job Description Responsible to coordinate and develop competitive and flexible strategies for potential awards in oncology and oncology-related indications, leveraging expertise, operational capabilities, and technologies to ensure client needs are addressed in the pre-award activities.Serves as the lead oncology strategist as assigned for potential awards...

Medicine moves forward here. So will you. Clinical trials, safety studies, and audits make safe and innovative pharmaceutical-led care possible. As part of Ergomed Group, you help patients benefit so they experience more of life’s meaningful moments. Biopharmaceutical companies are our clients. Patients are our purpose. Ergomed Group brings together...

Ergomed is seeking an EDC Developer to join the Data Management team. You will build EDC applications for complex projects, ensure data standards compliance, and support SDV activities under project leadership.The role focuses on Medidata RAVE and Zelta, CDASH/SDTM data standards, and seamless collaboration with cross-functional teams across Europe. Ideal...

Ergomed, a specialist CRO focusing on rare disease and oncology, is seeking an Oncology Strategy Lead to coordinate and develop competitive strategies for awards in oncology and related indications. You will leverage expertise and global capabilities to address client needs in pre-award activities.You will serve as lead oncology strategist for selected...

Ergomed, a global specialist CRO, is seeking a Specialist, Study Start Up and Regulatory Affairs to lead and coordinate study start-up and regulatory activities. You will ensure regulatory compliance and act as a key liaison among internal teams, clients, and external stakeholders.Responsibilities include delivering regulatory milestones, preparing essential...

Ergomed is seeking a Specialist, Study Start Up and Regulatory Affairs to lead and coordinate all activities related to achieving site initiation readiness. The role provides subject matter expertise, ensures regulatory compliance, and acts as a liaison between internal teams, clients, and external stakeholders.The successful candidate will manage...

Ergomed is seeking a Manager, Regulatory Registration and Compliance to lead regulatory projects and shape strategies across FDA, EMA, and other authorities. You will mentor juniors, manage budgets, and liaise with clients to ensure compliant submissions.The role requires leadership, EU regulatory knowledge, and excellent English communication, with a focus...

Ergomed is seeking a GCP audit professional to plan, conduct, and report complex audits across sponsor and site operations. You will work with a global client base in the pharmaceutical and biotechnology sectors, ensuring compliance with GCP, GVP, GMP, GLP, and related standards.The role emphasizes independent thinking, risk awareness, and collaboration...

Ergomed Group in Poland is seeking a pharmacovigilance professional to lead ICSR activities within our RA & PV network. You will manage ICSR processing, perform 2nd QC of cases, and act as the SME for the team.This role requires a life science or healthcare qualification and 5–6 years in pharmacovigilance, including line management. Strong communication,...