Clinical Supervision 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...

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 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 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...

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 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...

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...

Qlik Sense Developer We are looking for a Qlik Sense Developer with 4 to 5 years of experience to join our team. The ideal candidate will be proficient in Qlik Sense both ClientManaged and SaaS versions as well as experienced with Nprinting. Strong English language skills are require 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...

Business Development Representative supports our Business Development team in building and expanding the Milestone One network as well promotes and supports attracting new projects for Milestone One network of sites.In this role you will Build and sustain long 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...

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...

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...

Business Development Representative supports our Business Development team in building and expanding the Milestone One network as well promotes and supports attracting new projects for Milestone One network of sites.In this role you will Build and sustain long More...

GenePlanet is an innovative hightech company present in more than 35 countries. It started in 2008 with the dream that more and more people around the globe would have the chance to discover their DNA. They could change old habits enjoy the benefits of better nutrition and exercise in 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...

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...

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...