Clinical Management Jobs in Belgrade

David Kennedy Recruitment is working with a leadingB2B solution providerwho are looking to recruit aHead of Studio Management fortheir Gaming studios in Belgrade Serbia.Position:Head of Studio ManagementLocation: Belgrade SerbiaEmployment type: Fulltime Remuneration: Base salaryDUTIES More...

In collaboration with a leading B2B solution provider we are seeking a dynamic and experienced professional to join their team in Belgrade as the Head of Studio Management for their Gaming studios. Position: Head of Studio Management Location: Belgrade Serbia Employment Type: Fulltime More...

Position: Workforce Management SpecialistLocation: Belgrade SerbiaEmployment type: FulltimeWork model: onsite DUTIES AND RESPONSIBILITIES:Organize coordinate and supervise working schedules and rotations at gaming tables ensuring smooth operational flow and attendanceWork closely with More...

Exciting Opportunity: SAP Material Master Management Specialist Are you ready to take your expertise in Material Master Management to the next level We are looking for a skilled professional to join our team. What we are looking for Experience: 2 to 3 years in Material Master Manageme 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...

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...

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...

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...

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...

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...

Acting as the primary contact point for projectrelated matters Managing clients expectations to make sure the client is satisfied with services of PrimeVigilance and that the work PrimeVigilance delivers meets or even exceeds the clients expectations. Preparing project scope 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 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...

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...

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 Position: Operations Manager Company: Pro Coffee Gear Location: Remote (Anywhere) Full Time About Us: Pro Coffee Gear is a thriving ecommerce company located on our scenic 20acre ranch in Austin Texas. We specialize in providing toptier espresso machines and related parts to cof More...

POSITION SUMMARYThe Associate Quality Projects and Metrics supports the Quality Projects and Metrics Team inensuring that PrimeVigilances Quality and Compliance Metrics are compiled analyzed and reported incompliance with global regulations legislation and PrimeVigilance requirements. More...

Este es un puesto de trabajo remoto.This company is a dynamic global marketing company and worldwide leader in consumer generated content and marketing programs. We work with leading companies including Rowenta Barilla Huawei Nestle Samsung and others. Our online community of shopp More...

Infrastructure Engineer (Linux) About EXANTE EXANTE is a wealth tech company that provides centralized trading solutions and B2B financial infrastructure that helps create value through technology. Our proprietary trading platform enables market access to 1M financial instruments fr More...