Administrative Director Jobs in Belgrade

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...

Youll be working directly with the HR manager Youll provide support within the field of research and HR analytics Youll support in the preparation of presentations (for internal and external visits) Youll be supporting with the organization of HR projects Youll be supporting with the More...

Provides leadership and management of the QA team and business partners responsible for overseeing Quality Management System activities Provides input into the internal global audit program identifying risks and determining the number and types of audits to be conducted eac 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 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...

POSITION SUMMARYThe Associate Quality Projects and Metrics supports the Quality Projects and Metrics Team inensuring that PrimeVigilances Quality and Compliance Metrics are compiled analyzed and reported incompliance with global regulations legislation and PrimeVigilance requirements. 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...

Work closely with Project Manager and Operations to determine scope of work for initial contracts and/or change orders.Draft the initial contracts and/or change order with the information received from Operations and/or CommercialAct as primary client contact on small to midsized oppo More...

Work closely with Project Manager and Operations to determine scope of work for initial contracts and/or change orders.Draft the initial contracts and/or change order with the information received from Operations and/or CommercialAct as primary client contact on small to midsized oppo More...

At PSI Designer is responsible for creation and maintenance of specialized graphic materials that are used in the development of clinical trials documents. You will collaborate with global teams and provide guidance on design peculiarities for PSI departments. Hybrid in BelgradeY More...

COREnglish stands at the forefront of global online education and serves as a prominent resource for recruiting educators for schools across Asia.TasksThere are many benefits to working with our team but here are the main ones:Guaranteed hours!!! Schedule buildup****Hours are assigned 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...

COREnglish stands at the forefront of global online education and serves as a prominent resource for recruiting educators for schools across Asia.TasksThere are many benefits to working with our team but here are the main ones:Guaranteed hours!!! Schedule buildup****Hours are assigned More...

WHAT YOU WILL DO IN THIS POSITION:Oversee import activities for temperaturecontrolled and ambient regimes.Coordinate international transportation and ensure proper documentation for veterinary import permits.Ensure accuracy in import administration and data entry within the informatio More...

WHAT YOU WILL DO IN THIS POSITION:Oversee import activities for temperaturecontrolled and ambient regimes.Coordinate international transportation and ensure proper documentation for veterinary import permits.Ensure accuracy in import administration and data entry within the informatio More...

WHAT YOU WILL DO IN THIS POSITION:Provide legal assistance and advice to all departments and company directors.Monitor and interpret regulations relevant to the companys operations (corporate commercial trade law consumer protection competition labor law etc.).Represent the company in More...

Provide intelligence on requirements and contribute to the development of the strategy and set upactivities including Regulatory Management Plan joint operating procedures POAs and coredocuments. Support identification of issues. Perform regular screening of regulatory legislative req More...

Your role in the global Study Startup team will cover three main areas; Departmental support Quality Control and Assurance and Training. Departmental Responsibilities: Maintain trackers for the Study Startup departmentPrepare departmental reportsPlan organize and f More...

We are looking for a dedicated and skilled individual to lead our lighting team as the Lighting Operations Manager. This exciting role is ideal for someone with a passion for lighting technology operational efficiency and an unwavering commitment to excellence in execution.Key Respons More...