Calibration Procedures Jobs in Croatia

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...

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...

This is an exciting opportuniy for a freelancer / consultant to join our team as a Person Responsible for Local Literature Screening at 0.5 FTE.By working with us you will have the opportunity to work in an international team.Main responsibilitiesPerforming local scientific literature 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 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...

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...

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 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...

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 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...

Key Responsibilities:Prepare and manage marketing authorization (MA) submissions including the preparation of local administrative documents quality control (QC) and compilation. Provide ad hoc regulatory advice on submission packages in the postauthorization stage of the medicinal pr 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...

Line manages the team responsible for ICSR management for a selected project or group of projects Ensure adequate distrubution of tasks and oversees the workflow processOptimises procedures trainings and other actions to increase ICSR team efficiency Proposes process ch 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...

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...

CapsLock builds exceptional IT marketing solutions for large partners from North America. We create a unique marketing platform to deliver highquality service in different industries.CapsLock is looking to hire an outstanding Backend PHP Developer with solid technical skills to suppor More...

At this position responsibilities include:Supports Office Manager in the organization of the officeParticipates in organization of various events in the officePerforms duties regarding health and safety at workAssists in the onboarding process for new hiresAssists in implementing and 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 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 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...