QPL IQVIA RDS Poland

Please note that currently this position is fully on-site at the site in Metairie Louisiana. This site is scheduled to move to Kenner Louisiana after September 2025. Therefore this position will eventually be fully on-site in Kenner Louisiana. Join a collaborative patient-centered tea More...

Clinical Specialist Consultant - Hindi SpeakingLocation: Remote/virtualHours: Estimated 10-16h/monthRole: Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardiz More...

Job Title:Research AssistantWork Set-Up:Working On-siteScheduled Weekly Hours:24 HoursJob Profile Summary:This individual will play a key role in assisting in the conduct of clinical trial activities in accordance with all applicable regulations governing the conduct of clinical trial More...

Clinical Specialist Consultant - Polish SpeakingLocation: Remote/virtualHours: Estimated 10-16h/monthRole: Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardi More...

Senior Data Analyst HEOR (Oncology)Job OverviewIQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team working fully within the environment of a prominent Pharma company. This senior data analyst role sits within our Real World Solutions team and will be responsibl More...

Clinical Specialist Consultant - Romanian/Hungarian/Serbian/Dutch/Croatian and English SpeakingLocation: Remote/virtualHours: Estimated 10-16h/monthRole: Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that More...

Internal Job DescriptionJob Title:Clinical Research CoordinatorWork Set-Up:Working On-siteSchedule: 20 hours per week.Responsibilities:Phlebotomy is required and pediatric experience is also needed. Additionally community outreach will be part of the role.Perform a variety of complex More...

Job OverviewMaximize sales growth for full service clinical offerings consistent with Company strategy and objectives by using information technology and sales tools to effectively engage with target audiences. Achieves sales targets by researching and breaking into new accounts while More...

Job Title:Research AssistantWork Set-Up:Working On-siteScheduled Weekly Hours:24 HoursJob Profile Summary:This individual will play a key role in assisting in the conduct of clinical trial activities in accordance with all applicable regulations governing the conduct of clinical trial More...

*To be eligible for this position you must reside in the same country where the job is located*As an Associate Director in Clinical Project Management you will manage and support the operational elements and execution of studies and/or programs to ensure delivery; time and quality res More...

Job Overview: Part time - 32-40 hours/wk and onsite support.Coordinate and participate in clinical research studies ensuring that studies are carried out according toprotocol contracted scope of work good clinical practice sponsor standard operatingprocedures (SOPs) and any relevant l More...

Job OverviewSecure and retain business through professional consultative proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors.Essential FunctionsActively prospect and leverage potential new business opportunities within More...

We currently have the exciting opportunity to join the team as Clinical Trials Assistant or Senior CTA in full-time to work in our office in Warsaw.RESPONSIBILITIESPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up More...

Job OverviewManage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives.Essential Functions Manage staff in accordance with organizations policies and applicable regulati More...

Our team is growing join us on our mission to drive healthcare forward!ResponsibilitiesPerform site monitoring visits (selection initiation monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements i.e. Good Clinical Practice (GCP) and In More...

Job OverviewUnder general supervision perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May al More...

Job Overview:As a Senior Medical Writer on most types of writing projects you would prepare assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Perform Senior Review of straightforward medical w More...

Job Overview*For this role you must have at least 5 years of oncology experience as a CPMProject Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential me More...

JOB OVERVIEWThe Respiratory space is a priority growth area for IQVIA with a growing number of business opportunities in the space that require a specific level of experience for early engagement and to create a winning strategy. We are looking for a Therapeutic Strategy Lead who is e More...

As you develop your career as a CRA this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA we do not believe in a career ceiling. You can make the Senior CRA role a stepping-stone into wider opportunities like operations management More...