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/
530 Job openings in Ergomed
The Assistant Regulatory and PV Network will support the team with administrative tasks including tracking data retrieval planning document organisation and archiving to ensure smooth daily operation of the PrimeVigilance RA and PV Network department.Candidates will have the oppo More...
The Assistant Regulatory and PV Network will support the team with administrative tasks including tracking data retrieval planning document organisation and archiving to ensure smooth daily operation of the PrimeVigilance RA and PV Network department.Candidates will have the oppo More...
The Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) serves as the primary local representative to ensure compliance with national pharmacovigilance and regulatory requirements. This dual-role position is responsible for executing PV and RA a More...
The Assistant Regulatory and PV Network will support the team with administrative tasks including tracking data retrieval planning document organisation and archiving to ensure smooth daily operation of the PrimeVigilance RA and PV Network department.Candidates will have the oppo 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...
We are seeking a highly skilled Senior FP&A Analyst to join our dynamic finance team in Zagreb Croatia. As a key member of our Financial Planning and Analysis department you will play a crucial role in driving financial decision-making and supporting strategic initiatives across t More...
We are seeking a highly skilled Senior FP&A Analyst to join our dynamic finance team in Zagreb Croatia. As a key member of our Financial Planning and Analysis department you will play a crucial role in driving financial decision-making and supporting strategic initiatives across t More...
Pharmacovigilance Medical Writer Ii (aggregate Report Writing Experience Required)
We are looking for a pharmacovigilance medical writer to join our team. The Medical Writer will be responsible for medical writing including:PSURs/PBRERsPADERsACOsDSURsRMPsQC and review of all written output from the operations team as requiredSupporting the project managers to More...
Pharmacovigilance Medical Writer Ii (aggregate Report Writing Experience Required)
We are looking for a pharmacovigilance medical writer to join our team. The Medical Writer will be responsible for medical writing including:PSURs/PBRERsPADERsACOsDSURsRMPsQC and review of all written output from the operations team as requiredSupporting the project managers to More...
Pharmacovigilance Medical Writer Ii (aggregate Report Writing Experience Required)
We are looking for a pharmacovigilance medical writer to join our team. The Medical Writer will be responsible for medical writing including:PSURs/PBRERsPADERsACOsDSURsRMPsQC and review of all written output from the operations team as requiredSupporting the project managers to More...
Pharmacovigilance Medical Writer Ii (aggregate Report Writing Experience Required)
We are looking for a pharmacovigilance medical writer to join our team. The Medical Writer will be responsible for medical writing including:PSURs/PBRERsPADERsACOsDSURsRMPsQC and review of all written output from the operations team as requiredSupporting the project managers to 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...
PrimeVigilance is looking for a Medical Information Associate to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries in Polish and English. Responsibilities To provide approved responses to med More...
To review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/expectedness an More...
We are recruiting for a contract Project Manager with extensive experience running global trials in one of the following indications:RadiopharmaceuticalsGastrointestinal cancerLung cancerBreast cancerResponsibilities:Ensure that projects are delivered on time within budget and ag More...
We are recruiting for a contract Project Manager with extensive experience running global trials in one of the following indications:RadiopharmaceuticalsGastrointestinal cancerLung cancerBreast cancerResponsibilities:Ensure that projects are delivered on time within budget and ag More...
We are recruiting for a contract Project Manager with extensive experience running global trials in one of the following indications:RadiopharmaceuticalsGastrointestinal cancerLung cancerBreast cancerResponsibilities:Ensure that projects are delivered on time within budget and ag More...
We are recruiting for a contract Project Manager with extensive experience running global trials in one of the following indications:RadiopharmaceuticalsGastrointestinal cancerLung cancerBreast cancerResponsibilities:Ensure that projects are delivered on time within budget and ag More...
We are recruiting for a contract Project Manager with extensive experience running global trials in one of the following indications:RadiopharmaceuticalsGastrointestinal cancerLung cancerBreast cancerResponsibilities:Ensure that projects are delivered on time within budget and ag More...
We are recruiting for a contract Project Manager with extensive experience running global trials in one of the following indications:RadiopharmaceuticalsGastrointestinal cancerLung cancerBreast cancerResponsibilities:Ensure that projects are delivered on time within budget and ag More...
