Pracovné miesta v IQVIA v Slovensko

Job Overview · Provide Trial Master File (TMF) - Quality checks related assistance to study teams. · Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory requirements and meets qu ...

Senior Site Activation Coordinator – ICF (Informed Consent Form) · Locations: Bulgaria | Slovakia | Serbia| South Africa · Work Model: Hybrid · Make an impact on patient health with IQVIA · Join our Global Site Activation Team, a 2,000‑strong network driving high‑quality site act ...

Clinical Trial Educators collaborate with research staff to drive trial recruitment and support study-specific training needs. · Works with research sites to develop study-specific action plans to accelerate recruitment or support study-specific procedure trainingProvides educati ...

The DLM is responsible for the direct oversight and performance management of Partner employees assigned to Sponsor deployed to a given geographic and/or therapeutic area. · ...

Job Overview · Supports the Assoc Dir FP&A RWCS, EMEA. This role provides financial control of the EMEA RWCS and Overhead offering financials, including cost center management, preparation and/or controlling of forecasts/budgets, setting/reviewing cost and billing rates and servi ...

Clinical Trial Managers CTM are an integral part of clinical trial delivery leading and working alongside clinical teams to improve patients’ lives by bringing new drugs to the market faster. · Bachelor’s Degree in health care or other scientific discipline required · Ideally at ...

Sr. QA Auditor, GCP position involves planning and conducting independent audits to assess compliance with regulations. · Plan, schedule, conduct, report and close audit activities in any of the countries involved with IQVIA contracts to assess compliance with applicable regulati ...

We're looking for a Senior Talent Search Recruiter to help shape how we identify and engage top talent across the business. · Partner with recruiters and hiring managers as a strategic search expert · Lead intake discussions and design effective sourcing strategies · ...

IQVIA is seeking a Project Support Coordinator to provide administrative support to the field based staff of complex multiple projects. · ...

Job Overview · Supports the Assoc Dir FP&A RWCS, EMEA. This role provides financial control of the EMEA RWCS and Overhead offering financials, including cost center management, preparation and/or controlling of forecasts/budgets, setting/reviewing cost and billing rates and servi ...

This is a compensation and benefits manager role with a focus on providing compensation program management and execution. The role involves delivering education and communication of annual and off-cycle compensation planning processes for IQVIA employees working in the EMEA Busin ...

We are looking for a Language Assets Specialist to work within our Language Quality services team. The role is a Full-time, home-based opportunity in Europe. · Proactively detect needs for glossary creation. · ...

IQVIA is seeking a Project Support Coordinator to provide administrative support to field-based staff of complex multiple projects. · ...

We are looking for a Senior Machine Learning Engineer to lead the design and development of ML applications across our product portfolio. · Lead the design and development of ML applications. · Evaluate current and emerging industry tools, techniques, and algorithms. · Mentor jun ...

The Associate Global Site ID Lead will direct and manage the execution of strategic operational and financial delivery of required site activation activities. · ...

As a Senior Site Activation Coordinator, under general supervision, you will perform tasks at a country level associated with site activation activities. · ...

+Provide Trial Master File (TMF) - Quality checks related assistance to study teams. · +Bachelor's degree or equivalent/li>3-4 years' experience working in a Records Management technically-related area./li>Good knowledge of applicable clinical research regulatory requirements,/li ...

The Clinical Project Lead is an integral part of clinical trial delivery. · ...

Perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations. · ...

Provide Trial Master File (TMF) quality checks related assistance to study teams. Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices and meets quality and timeline metrics. · ...