Clinical Supervision Jobs in Belgrade

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...

The Senior 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 saf More...

The Specialist/Senior Specialist Study Start Up and Regulatory is responsible for completing study startup and regulatory deliverables based on an established SSU  RA management plan. They also serve as a liaison between SSU/regulatory project team authorities vendors and investi More...

At PSI Designer is responsible for creation and maintenance of specialized graphic materials that are used in the development of clinical trials documents. You will collaborate with global teams and provide guidance on design peculiarities for PSI departments. Hybrid in BelgradeY More...

Ergomed is looking for a Regulatory Affairs professionals with indepth 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 we More...

Key Responsibilities:Oversee endtoend recruitment processes across multiple countries ensuring highquality talent acquisition.Manage onboarding and offboarding processes ensuring compliance with company standards and local regulations.Develop implement and improve HR policies procedur More...

The Medical Reviewer I is responsible for medical review of lCSRs and literature review writing of signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS/PBRERs/PADERS) as required by the Company or Client. Responsibilities include:To revie More...

Job DescriptionThe Medical Reviewer II is responsible for medical review of lCSRs and literature review writing signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS/PBRERs/PADERS) as required by the Company or Client. For the Client:To re More...

This is an opportunity for new graduates to start and develop their career within drug safety. The Medical Writing Assistant will be working as part of a medical writing team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilanceHandling (trackin 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...

Job DescriptionHi there!We are Semrush a global IT company developing our own product a platform for digital marketers. New stars are born here so dont miss your chance. This is our Customer Support Frontline Specialist role for those who can find a common language with anyone in the More...

The Senior Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs writing and reviewing signal detection reports writing and/or reviewing aggregate reports (DSURS PSURS/PBRERs/PADERS ACOs responses to regulatory authority requests) writing and/or reviewing risk More...