Search the 25 jobs at Ergomed

The Senior Safety Technology Support Specialist is responsible for leading support related to safety databases and technological applications used in pharmacovigilance. Duties include gathering user requirements, liaising with the Safety Systems team, participating in audits and testing, and providing user training. The role also involves maintaining SOPs, assisting with regulatory needs, and mentoring junior staff while supporting the implementation of safety system enhancements and efficiencies.

The Regional People Generalist is responsible for administering HR policies and operations, supporting onboarding and offboarding, managing employee documentation, and providing HR-related advice. They will also facilitate talent management programs and ensure compliance with labor regulations while promoting a conflict-free workplace.

The IT Technical Support Engineer provides technical support to internal and external users, manages support tickets, performs troubleshooting, and maintains company systems including laptops and servers. They are responsible for responding to incidents, documenting resolutions, and training personnel in IT procedures.

The PV Associate/Literature will be responsible for supporting literature monitoring, screening activities, assisting with literature search strategies, reviewing literature articles, tracking data, and ensuring compliance with regulations. The role requires strong communication, organizational skills, and attention to detail while working under supervision and assisting with the development of screening processes.

The PV Associate/Literature assists in literature monitoring ensuring compliance with regulations, contributes to company goals, and participates in literature searches and screenings. They maintain records and track literature, assist in quality checks, and support the team in regulatory inspection preparedness.

The PV Associate role is designed for recent graduates in life sciences or healthcare fields. Responsibilities include processing safety reports, reconciling received reports, and supporting pharmacovigilance activities while working under supervision. The position emphasizes training, teamwork, and a proactive approach to patient safety.

The role involves monitoring local scientific literature and safety web portals for adverse event reports. Responsibilities include formulating search strategies, translating relevant documents, maintaining files according to procedures, and ensuring compliance with data privacy and security standards.

The role involves performing local scientific literature monitoring for adverse event reports, formulating search strategies, providing translations of documentation, and ensuring compliance with data privacy and security procedures.

The PV Associate role involves processing Individual Case Safety Reports and supporting pharmacovigilance activities, ensuring compliance with regulations and high-quality data management. The position is aimed at new graduates looking to start their career in drug safety and includes mentoring from experienced colleagues.

Planning, preparation, conduct, reporting and follow up of various types of GCP audits according to expected quality and timelines. Executing audits based on a comprehensive understanding of all regulatory requirements and Good Clinical Practice (GCP). Performing GCP quality assurance projects on behalf of client companies within the pharmaceutical/biotechnology industry. Assisting with business development activities.

The PV Administrative Assistant will support pharmacovigilance activities, including tracking safety messages, filing Individual Case Safety Reports, submitting reports, and preparing documents. Required skills include good IT proficiency and strong attention to detail. Training will be provided, making prior experience unnecessary.

As a PV Assistant, you'll support pharmacovigilance activities, manage safety messages, track Individual Case Safety Reports (ICSRs), and prepare periodic reports. Training will be provided, focusing on compliance and documentation accuracy.

The PV Assistant will support pharmacovigilance activities by managing safety messages, tracking Individual Case Safety Reports (ICSRs), and maintaining archives. Training will be provided, and the role requires strong organizational and communication skills.

The QA Associate will assist the QA team in managing and conducting internal and external audits in accordance with PrimeVigilance procedures, support audit scheduling and tracking, and maintain documentation related to audits and CAPA activities.

The Benefit/Risk Associate will participate in signal detection activities, review line listings, draft signal detection reports, maintain relevant tracking tools, and collaborate with other departments to ensure compliance with procedures and regulatory requirements.

The Accounting Assistant will provide support to the Finance Department by processing invoices, communicating with vendors regarding payments, ensuring approval, archiving documentation, and collaborating with team members. This role requires attention to detail and effective communication skills.

The PV Associate/Literature is responsible for literature monitoring, assisting with literature searches and screenings, and ensuring compliance with safety services for pharmaceutical companies. The role involves data tracking, peer review quality control, and preparing for regulatory inspections.

The PV Associate will support pharmacovigilance activities, processing Individual Case Safety Reports, and reconciling reports while working under supervision. This entry-level position is designed for recent graduates with life science backgrounds looking to start their careers in drug safety.

The role requires monitoring local scientific literature for adverse event reports, refining search strategies, providing translation or revisions of documents, and maintaining files according to PrimeVigilance procedures. This position is suited for a freelancer with a life sciences background and fluency in both German and English.

The role involves local scientific literature and safety web portal monitoring for adverse event reports, formulating search strategies, translating relevant documentation, and maintaining proper file organization in compliance with PrimeVigilance procedures.