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/
536 Job openings in Ergomed
Manages and mentors the safety reporting staff in the ICSR Management UnitEnsures adequate distribution of tasks for assigned safety reporting staff and oversees the workflow processOperates as the link between Regulatory Intelligence Department and ICSR Management Unit to ensure accu More...
Manages and mentors the safety reporting staff in the ICSR Management UnitEnsures adequate distribution of tasks for assigned safety reporting staff and oversees the workflow processOperates as the link between Regulatory Intelligence Department and ICSR Management Unit to ensure accu More...
Manages and mentors the safety reporting staff in the ICSR Management UnitEnsures adequate distribution of tasks for assigned safety reporting staff and oversees the workflow processOperates as the link between Regulatory Intelligence Department and ICSR Management Unit to ensure accu More...
Position SummaryThis role requires working as part of the Safety System Administrator Team performing database administration activities; supporting creation and upgrade of database instances; change control and data migration activities; first line user support and troubleshooting; a More...
Manages and mentors the safety reporting staff in the ICSR Management UnitEnsures adequate distribution of tasks for assigned safety reporting staff and oversees the workflow processOperates as the link between Regulatory Intelligence Department and ICSR Management Unit to ensure accu More...
Position SummaryThis role requires working as part of the Safety System Administrator Team performing database administration activities; supporting creation and upgrade of database instances; change control and data migration activities; first line user support and troubleshooting; a More...
Position SummaryThis role requires working as part of the Safety System Administrator Team performing database administration activities; supporting creation and upgrade of database instances; change control and data migration activities; first line user support and troubleshooting; a More...
Manages and mentors the safety reporting staff in the ICSR Management UnitEnsures adequate distribution of tasks for assigned safety reporting staff and oversees the workflow processOperates as the link between Regulatory Intelligence Department and ICSR Management Unit to ensure accu More...
Position SummaryThis role requires working as part of the Safety System Administrator Team performing database administration activities; supporting creation and upgrade of database instances; change control and data migration activities; first line user support and troubleshooting; a More...
Position SummaryThis role requires working as part of the Safety System Administrator Team performing database administration activities; supporting creation and upgrade of database instances; change control and data migration activities; first line user support and troubleshooting; a More...
Manages and mentors the safety reporting staff in the ICSR Management UnitEnsures adequate distribution of tasks for assigned safety reporting staff and oversees the workflow processOperates as the link between Regulatory Intelligence Department and ICSR Management Unit to ensure accu More...
Senior Specialist, Pharmacovigilance (pv Regulatory Experience Required)
The Senior Specialist Regulatory and PV Network is responsible for developing the strategy based on regulatory requirements and for driving regulatory and PV deliverables based on an established PV and regulatory plan. They also serve as a liaison between regulatory and other function More...
The position is primarily responsible for the creation maintenance and review of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clients activities More...
The position is primarily responsible for the creation maintenance and review of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clients activities 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 English & French. Responsibilities To provide approved responses to m 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 English and French. Responsibilities To provide approved responses to med 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 English and French. Responsibilities To provide approved responses to med More...
The position is primarily responsible for the creation maintenance and review of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clients activities More...
We are recruiting for a contract Project Manager or contract Clinical Team Manager wiuth previous experience running global trials in Radiopharmaceuticals Gastrointestinal / Lung / Breast Cancer or Duchenne Muscular Dystrophy. Ensure that projects are delivered on time More...
The PV Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.) This is an opportunity for new graduates to start and develop their career within drug safety. Th More...
