QPL IQVIA RDS Poland

Job SummaryPlans directs and leads key Account Management structure for Patient Insights Experience and Registry Solutions (PIERS) teams for key accounts in the US region. Responsible for multiple accounts based upon practice needsEssential FunctionsDirects the activities of Account S More...

Job OverviewPerform analysis and reporting of Phase I-IV clinical pharmacology studies such as dose tolerance dose proportionality mass balance concept testing bioavailability thorough QTc drug-drug interactions and special population (age effects renal disease hepatic disease gender More...

Clinical Specialist Consultant - Greek 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 Overview:Line Management responsibilities for direct reports managing the accounting activities within the Avacare site network. To ensure timely and accurate accounting and reports in accordance with IQVIA Finance Standard Operating Procedures (SOPs) US Generally Accepted Account More...

Job Summary:This position is responsible for the development of the end to end design of client standards and study specifications that align to the CDISC standards and regulatory agency guidances. This position provides this guidance and training to clients of IQVIA.Job Responsibilit More...

Job OverviewReview assess and process safety data and information across service lines from various sources. Distribute reports/data to internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines with guidance and s More...

Senior Clinical Bioinformatics Data ScientistLocation: home-based anywhere in the United States onlyJob Overview:IQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team working fully within the environment of a prominent Pharma company supporting biomarker and trans More...

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...

Major duties and Responsibilities:Perform phone calls to reporter (physicians office Health Care Professionals (HCP) and consumers) to obtain follow up information on case reports of death unexplained or other events of interest as directed. Utilize medical judgement when reviewing ca More...

Are you a Registered Nurse interested in Clinical Trial workIQVIA is looking for qualified Registered Nurses interested in community and clinical trial work to visit clinical trial patients in their homes. You will be responsible for going to patient homes to assist with conducting re More...

To be eligible for this position you must reside in the same country where the job is located.PURPOSE Direct clinical monitoring operations for a designated IQVIA regional office or group to ensure projects are appropriately resourced and employees are trained and developed to meet pr More...

Job OverviewThe Medical Director will provide medical clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide ther 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...

This is a fully on-site position at the site in Springville Utah. Overview:Coordinate and participate in clinical research studies ensuring that studies are carried out according to protocol contracted scope of work good clinical practice sponsor and Avacare standard operating procedu 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...

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...