Clinical Management Jobs in Croatia

As a Milestone One Site Coordinator you will supports study sites in all trial related activities according to ICHGCP protocol requirements within Study specific defined timelines and enrollment goals.Based in Zagreb CroatiaIn this role you will:Act as the main line of communicat More...

As a WFM Planner you will join a dynamic Workforce Management team collaborating with 56 other WFM planners to own and deliver capacity plans for your region. You will work closely with a dedicated WFM Analyst and be supported by a Global Planning Lead to ensure datadriven decisionmak More...

As a Workforce Management Specialist in our dynamic Workforce Management (WFM) team you will play a pivotal role in designing and maintaining the schedules that ensure we deliver exceptional service to our customers. You will work closely with the WFM Lead Planning and Intraday functi More...

Kontinuirano planiranje organiziranje i kontroliranje rada podreenog timaPruanje povratnih informacija motiviranje obuavanje i pruanje strune podrke timuRezultati tima izvjetavanje i poduzimanje korektivnih mjera ako je potrebnoSvakodnevni rad tima s ciljem postizanja individualnih i More...

Training consultation and support of Study Site Coordinators /Research Nurses on clinical studiesProviding nonoperational site support to ensure progress of clinical study and to ensure that it is conducted recorded and reported in accordance with the protocol standard operating proce More...

The Senior Manager of Quality Management is responsible for leading one or more teams within Quality Management in line with global strategic objectives. The Senior Manager of Quality Management collaborates with global operational functions to ensure Pharmacovigilance and Medical Inf More...

The Quality Management Officer is responsible for ensuring that Quality Events (QEs) and Corrective and Preventative Actions (CAPAs) are completed in accurate and timely fashion and are managed in compliance with global regulations legislation and PrimeVigilance requirements.Lead the More...

Data management: Understands project budgets. Represents budget in Resource Hero (Resource database).Compares and reconciles data sets.Manages resource records correctly for starters leavers returners and movers in Resource Hero.Identifies issues and escalates.Reporting and insig More...

The Quality Management System & Training Compliance Specialist is responsible for:Providing adhoc support for all QM&C activities both globally and crossfunctionally. These responsibilities may include but are not limited to assisting in the development/revision of QM&amp 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...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.Hybrid work in ZagrebResponsibilities:Medical point of contact for internal project team study sites and st More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.Hybrid work in ZagrebResponsibilities:Medical point of contact for internal project team study sites and st 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 PrimeVigilance Senior PV Associates are experienced case processing team members who are expected to manage a variety of case processing services with minimal guidance from senior team members. If you join PrimeVigilance you can expect to work with teams of different sizes fro 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...

For the Client:To review and approve postmarketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/e More...

The Benefit/Risk Officer should be a Life science / bio medical background graduate preferably pharmacist with an experience in signal detection and use of signal management tools. The Benefit/Risk Officer will be working as part of a project team performing and supporting contracted 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 review a More...