About Ergomed
Ergomeds fast-growing services business includes an industry-leading suite of specialist pharmacovigilance solutions, integrated under the PrimeVigilance brand and a full range of high-quality clinical research and trial management services under the Ergomed Clinical Research brand. The Ergomed group employs over 1,800 people and operates out of 24 offices around the world, providing its services to researchers and patients in around 100 countries globally. Our Ergomed Clinical Research business was founded in 1997 and provides high-quality clinical research and trial management services globally and across all trial phases (I to IV), specialising in oncology and rare disease trials. We use innovative site-support services which focus on enhancing patient recruitment and engagement, with a strong heritage in Europe and the USA. PrimeVigilance is a global leader in pharmacovigilance and specialised multi-lingual medical information services. Since 2008, the PrimeVigilance business has supported pharmaceutical, biotechnology and genetics companies in managing the global safety of their products, all the way from clinical trial to post-marketing. Our pharmacovigilance services include case processing, signal and risk management, pharmacoepidemiology, audits, training, advisory literature services, medical information and QPPV. Website http://www.ergomedcro.com/
525 Job openings in Ergomed
To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and Company causality as well as writing of More...
To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and Company causality as well as writing of More...
To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and Company causality as well as writing of More...
To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and Company causality as well as writing of More...
The Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs and literature review writing signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS PBRERs PADERS). To review and approve post-marketing Individual Case Safety R More...
To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and Company causality as well as writing of More...
To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and Company causality as well as writing of More...
Engaging in everyday tasks working on tickets and maintaining oversight of personal and group tickets to ensure timely resolution.Closing and meticulously documenting resolutions or workarounds in the internal knowledgebase to facilitate knowledge sharing and improve future problem-so More...
Engaging in everyday tasks working on tickets and maintaining oversight of personal and group tickets to ensure timely resolution.Closing and meticulously documenting resolutions or workarounds in the internal knowledgebase to facilitate knowledge sharing and improve future problem-so More...
To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and Company causality as well as writing of More...
To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and Company causality as well as writing of More...
The PV Assistant will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you join More...
To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and Company causality as well as writing of More...
The Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs and literature review writing signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS PBRERs PADERS). To review and approve post-marketing Individual Case Safety R More...
We are looking to hire an experienced Accountant to join our team in our growing office in Zagreb.The Accountant role is a varied one covering various accounting responsibilities:Post supplier invoices expense reports and journals for small entities in accordance with our accounting g More...
The Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs and literature review writing signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS PBRERs PADERS). To review and approve post-marketing Individual Case Safety R More...
Primary responsibility is to ensure that the safety Reporting and Exchange with Client partners activities are managed in a cost-efficient manner of the highest quality and in compliance with global regulations and company policies and in accordance with any PV agreement. Ot More...
Primary responsibility is to ensure that the safety Reporting and Exchange with Client partners activities are managed in a cost-efficient manner of the highest quality and in compliance with global regulations and company policies and in accordance with any PV agreement. Ot More...
We are looking to hire an experienced Accountant to join our team in our growing office in Zagreb.The Accountant role is a varied one covering various accounting responsibilities:Post supplier invoices expense reports and journals for small entities in accordance with our accounting g More...
At PrimeVigilance PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability. If you join PrimeVigilance you can expect to work with teams of different sizes from small clinical trial to More...
