Clinical Development Jobs in Deszczno

Main Purpose of RoleTo centrally manage a Lean and compliant Quality Management system for medical devices schemes (Medical includes Notified Body NB1639 UKCA ISO 13485 MDSAP and all other Medical Schemes at SGS)Management of external audits and communication with competent authorityM More...

 We are seeking a highly skilled Regulatory Manager to oversee the clinical and performance evaluation components of our medical device conformity assessment process within Notified Body 1639. This role is vital to ensuring regulatory excellence clinical integrity and t More...

The Senior Pharmacovigilance (PV) Physician I is responsible for medical review of ICSRs writing and/orreviewing signal detection reports writing and or reviewing aggregate reports (DSURS PSURS PBRERs.PADERS) reviewing risk management reports (RMPs) and mentoring junior PV Physicians. More...

For our clientsTo 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 listedness/expectedness and company causal More...

The Medical Director will lead educate mentor and develop the team of PV physicians to ensure their competence and confidence in developing their skills to become subject matter experts in pharmacovigilance. The role requires active monitoring of costs and project deliverables and int More...

This is a remote position.We are looking for a Veeva Vault SME who can provide guidance and expertise services for the clinical part of the Development Cloud solutions of Veeva Vault. The Development Cloud is a suite of applications that helps life sciences companies streamline the More...