حول 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/
545 فرصة عمل في Ergomed
Pharmacovigilance Officer, Team Leader (line Management Position)
Providing support to other activities undertaken by the project team on behalf of the client and the company Performing activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to): Processing Individual Case Safety Report المزيد...
The Manager Study Start Up and Regulatory is responsible for developing the strategy based on regulatory requirements and for completing study start-up and regulatory deliverables based on an established regulatory SSU RA management plan. They actively assist senior management i المزيد...
Pharmacovigilance Officer, Team Leader (line Management Position)
Providing support to other activities undertaken by the project team on behalf of the client and the company Performing activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to): Processing Individual Case Safety Report المزيد...
Ergomed is looking for a Regulatory Affairs professionals with in-depth experience in managing global complex clinical studies.Opportunities are open to any geographical location; however candidates will be required to possess excellent written and communication skills in English as w المزيد...
Pharmacovigilance Officer, Team Leader (line Management Position)
Providing support to other activities undertaken by the project team on behalf of the client and the company Performing activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to): Processing Individual Case Safety Report المزيد...
The Manager Study Start Up and Regulatory is responsible for developing the strategy based on regulatory requirements and for completing study start-up and regulatory deliverables based on an established regulatory SSU RA management plan. They actively assist senior management i المزيد...
Local Contact Person For Pharmacovigilance And Regulatory Affairs (lcppv/lcpra) - English & German
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 المزيد...
The Manager Study Start Up and Regulatory is responsible for developing the strategy based on regulatory requirements and for completing study start-up and regulatory deliverables based on an established regulatory SSU RA management plan. They actively assist senior management i المزيد...
Pharmacovigilance Officer, Team Leader (line Management Position)
Providing support to other activities undertaken by the project team on behalf of the client and the company Performing activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to): Processing Individual Case Safety Report المزيد...
Pharmacovigilance Officer, Team Leader (line Management Position)
Providing support to other activities undertaken by the project team on behalf of the client and the company Performing activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to): Processing Individual Case Safety Report المزيد...
The Manager Study Start Up and Regulatory is responsible for developing the strategy based on regulatory requirements and for completing study start-up and regulatory deliverables based on an established regulatory SSU RA management plan. They actively assist senior management i المزيد...
The Manager Study Start Up and Regulatory is responsible for developing the strategy based on regulatory requirements and for completing study start-up and regulatory deliverables based on an established regulatory SSU RA management plan. They actively assist senior management i المزيد...
The Manager Study Start Up and Regulatory is responsible for developing the strategy based on regulatory requirements and for completing study start-up and regulatory deliverables based on an established regulatory SSU RA management plan. They actively assist senior management i المزيد...
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 المزيد...
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 المزيد...
Ergomed is looking for a Regulatory Affairs professionals with in-depth experience in managing global complex clinical studies.Opportunities are open to any geographical location; however candidates will be required to possess excellent written and communication skills in English as w المزيد...
Provide intelligence on requirements and contribute to the development of the strategy and set upactivities including Regulatory Management Plan joint operating procedures POAs and coredocuments. Support identification of issues. Perform regular screening of regulatory legislative req المزيد...
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 المزيد...
Local Contact Person For Pharmacovigilance And Regulatory Affairs (lcppv/lcpra)
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 in the United States. This dual-role position is responsible for المزيد...
Local Contact Person For Pharmacovigilance And Regulatory Affairs (lcppv/lcpra)
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 in the United States. This dual-role position is responsible for المزيد...
