Regulatory Strategy Jobs in Croatia

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...

The Assistant Regulatory and PV Network will support the team with administrative tasks including tracking data retrieval planning document organisation and archiving to ensure smooth daily operation of the PrimeVigilance RA and PV Network department.Candidates will have the oppo 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...

Wolt is a Finnish technology company and were best known for our food delivery platform. We are growing rapidly and are now looking for an Operations Associate to join our Operations team in Croatia.In the Operations Team we focus on our courier partners: We ensure the right amount of More...

Are you a Public Policy professional with proven work experience and a genuine interest in the evolving policy and regulatory landscape of the platform economy Do you want to be a part of building and scaling a truly global tech organization in Southeast Europe If this sounds like you 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...

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 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...

Assures and exerts activities leading to effective cooperation with clients in the area of literature monitoringContributes to achieving companys goals and objectivesEnsures that the Literature Screening responsibilities and activities are managed in a costefficient manner of the high More...

Assures and exerts activities leading to effective cooperation with clients in the area of literature monitoringContributes to achieving companys goals and objectivesEnsures that the Literature Screening responsibilities and activities are managed in a costefficient manner of the high More...

The Senior Pharmacovigilance (PV) Physician I is responsible for medical review of ICSRs writing and/or reviewing signal detection reports writing and or reviewing aggregate reports (DSURS PSURS PBRERs. PADERS) reviewing risk management reports (RMPs) and mentoring junior PV Phys More...

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...

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...

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...

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...

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...

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...

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...

Paymentology is the first truly global issuerprocessor giving banks and fintechs the technology team and experience to rapidly issue and process Mastercard Visa and UnionPay cards across more than 60 countries at scale. Our advanced multicloud platform offering both shared and dedicat More...

Join our local team of Product Designers with unique product strategy expertise. Our clients value us for our strategic partnership exceptional craft and ability to deliver real business results. Weve helped hundreds of organizations including large enterprises small businesses a More...