Jobs in Orebić

Job DescriptionAs a Talent Acquisition Partner you will:Work closely with one or multiple scaling companies in Europe.Set up hiring processes scorecards interviews and analytics for each process.Communicate and strengthen relationships on a regular basis with key stakeholders.Be respo 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...

Research for the available options for vendors to find the best prices available within a given market/territoryCooperate with other departments/entities within the group to explore the available options for providing services in houseMaintain the list of available options with detail More...

BwB is one of the lead partners in a consortium of European institutions who have been mandated to work with European cities to implement action and finance their Net Zero Investment Plans to reach carbon neutrality by 2030. This mandate known as NetZeroCities (NZC) is an initiative l More...

The Executive VP Pharmacovigilance (PV) Operations is responsible for leading and overseeing all operational aspects of global pharmacovigilance activities ensuring compliance with regulatory requirements company SOPs and industry standards. This role will manage PV teams optimize ope More...

We are looking to hire an experienced Accountant to join our team in our growing office in Zagreb.The Accountant role is a varied one covering various accounting responsibilities:Post supplier invoices expense reports and journals for small entities in accordance with our accounting g More...

Benefit-Risk AssistantThe Benefit-Risk Assistant will be working as part of Benefit-Risk Management Department performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will recei More...

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 More...

As the ESG & Corporate Officer you will lead the design implementation and governance of Environmental Social and Governance (ESG) initiatives across our global operations. You will work cross-functionally with internal departments and external partners to embed our ESG strategy i More...

We are currently seeking reinforcements for our team working on an award-winning learning platform for one of our American clients which aims to increase the literacy of students and teachers in the US. There are several existing products within the platform each with a different targ More...

The Snr. Project Manager is responsible for the planning management and control projects run by the IT team in the delivery of technology to the Ergomed business and the delivery and hand over of the systems and capabilities into the production systems and business environments within More...

For the Client (May include but is not limited to the following):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 seri 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...

Position Summary - Summary of Key ResponsibilitiesThe Senior Quality Assurance Manager ensures continuous quality improvement through effective management and oversight of Audits and Inspections. Facilitates ongoing quality improvement measures through communication of audit & Ins 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...

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 More...