Regulations Technician Jobs in Croatia

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 Title: Property Manager Location: Remote (Ability to work within specified time zones as needed) Salary Range: Up to 1000 USD Work Schedule: Monday Friday 9:00 AM to 5:00 PM (US Working Hours) About Sagan: Sagan is an exclusive highperformance membership community designed to con 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...

As a Quality Control Inspector youll be reporting to an Operations Manager and working as a part of our Operations team. At QIMA the role of Operations is to deliver our industryleading services to our clients while ensuring that all the work is performed to the QIMA standard of quali 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 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...

Oversee the management and optimization of all IaaS PaaS and SaaS infrastructure to ensure it meets the needs of the business.Implement and manage monitoring tools to ensure high performance and availability of IaaS PaaS and SaaS products.Develop and implement the global IT Infrastruc 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 EU QPPV is responsible for:The establishment and maintenance of a system which ensures that information about all suspected adverse reactions which are reported to the personnel of the Company and to medical representatives is collected and collated in order to be accessible at le 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...

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 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 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 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...

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...

About the job Are you enthusiastic about languages proficient in German and eager to explore the fastpaced field of content moderation If so this is a fantastic opportunity to join our team in the vibrant city of Lisbon! Whether youre an industry veteran or just beginning your career More...

About the job Are you enthusiastic about languages proficient in German and eager to explore the fastpaced field of content moderation If so this is a fantastic opportunity to join our team in the vibrant city of Lisbon! Whether youre an industry veteran or just beginning your career More...

About the job Are you enthusiastic about languages proficient in German and eager to explore the fastpaced field of content moderation If so this is a fantastic opportunity to join our team in the vibrant city of Lisbon! Whether youre an industry veteran or just beginning your career 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...

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...