Empregos para ergomed em Lisboa

Ergomed Group in Lisbon seeks a Team Leader for ICSR management to guide a project team and ensure effective distribution of tasks, maintaining strong client collaboration. The role requires life science background with pharmacovigilance experience and proven line management skills, plus excellent communication, organization and planning abilities to drive...

Ergomed is seeking a pharmacovigilance professional to support project activities and manage ICSR processing with quality control. You will contribute to KPI creation and process improvements while collaborating with cross-functional teams.The role includes acting as Local Contact Person for pharmacovigilance and language-specific responsibilities within the...

Ergomed Group is seeking a Medical Information Associate with Italian language to support the Medical Information team in handling initial adverse event and medical information inquiries. The role involves providing approved responses to inquiries in Italian and English, accurately identifying and reporting adverse events, and documenting all inquiries in...

Ergomed invites applications for a role in Medical Information to develop knowledge in pharmacovigilance and expand the medical information function. You will handle inquiries in English and Italian, provide accurate responses, and collaborate with physicians and client teams to ensure high quality information delivery.The role emphasizes customer service,...

Ergomed Group is seeking a Senior Director / Executive Director Medical Writing to lead the PV Medical Writing function and uphold high-quality, compliant deliverables across projects. This role reports to the Senior Leadership Team and drives strategic PV expertise for clients and internal teams. The position also involves developing the PV Medical Writing...

Ergomed Group in Lisbon seeks a Medical Information Associate with Dutch language to support the Medical Information team handling adverse events and information inquiries. You will respond in Dutch and English, document events, and assist in 24/7 support if contracted. A healthcare-related degree and strong communication are essential.Join a global...

Ergomed is seeking a Senior Specialist, Study Start Up and Regulatory Affairs to lead and coordinate initiation activities, ensuring regulatory compliance and timely submissions across sites.You will draft and review essential documents, manage multi-country SSU requirements, and provide strategic input to internal and external stakeholders to support...

Company Description Medicine moves forward here. So will you. Medicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early...

Medicine moves forward here. So willyou. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing surveillance....

Company Description Medicine moves forward here. So will you. Company Description Medicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every...

Medicine moves forward here. So will you.At PrimeVigilance, patient safety is not one part of the job. It is why we exist.We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing surveillance. Increasingly,...

Medical Information Associate Dutch LanguageFull-timeDepartment: PV Medical InformationMedicine moves forward here. So will you.At PrimeVigilance, patient safety is not one part of the job. It is why we exist.We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every...

Medicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post‑marketing surveillance....

Company Description Medicine moves forward here. So will you. Company Description Medicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every...

Company Description Medicine moves forward here. So will you. Company Description Medicine moves forward here. So will you. Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. We focus on the most complex trials, the studies where experience, judgement, and rigorous operational accountability make...

Senior Director / Executive Director Medical Writing Full-time Department: Medical Writing Medicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of...

PrimeVigilance in Lisbon is seeking a Senior Director / Executive Director Medical Writing to lead the PV Medical Writing function, ensuring high-quality, compliant, and timely deliverables.As a senior member of the leadership team, you will oversee the PV Medical Writing group, drive quality, inspection readiness, and contribute to strategic client...

**Company Description** Ergomed Group is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee...

Ergomed Group in Lisbon is seeking a Senior Specialist, Study Start Up and Regulatory Affairs to lead and coordinate activities to achieve site initiation readiness. You will provide regulatory expertise and ensure ICH-GCP compliance while serving as a key liaison between internal teams, clients and external stakeholders.Responsibilities include delivering...

Specialist/Snr Specialist Study Start Up and Regulatory AffairsFull-timeDepartment: Study Start up and Regulatory UnitMedicine moves forward here. So willyou.Ergomedis a specialist clinical research organization focused on rarediseaseand select oncology indications. We focus on the most complextrials,the studies where experience, judgement, and rigorous...