QPL IQVIA RDS Poland

Internal Job DescriptionJob Title:Clinical Research CoordinatorWork Set-Up:Working On-siteSchedule: 24 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...

Provides data management support oversight and/or accountability for one or moreclinical trials.Take the lead with the trial customer(s) and other internal and externalpartners to establish align and confirm data management expectationsCreating planning and tracking content format qua More...

Job Overview: Part time - 48 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 loca More...

Job OverviewIQVIA is seeking a detail-oriented Intern to join our team in Warsaw. This internship offers the opportunity to support clinical trial documentation processes and gain valuable experience in a global Contract Research Organization (CRO). You will work closely with experien More...

Job Title:Research AssistantWork Set-Up:Working On-siteScheduled Weekly Hours:40 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...

Internal Job DescriptionJob Title:Clinical Research CoordinatorWork Set-Up:Working On-siteSchedule: 24 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...

Internal Job DescriptionJob Title:Clinical Research CoordinatorWork Set-Up:Working On-siteSchedule: 24 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...

Internal Job DescriptionJob Title:Clinical Research CoordinatorWork Set-Up:Working On-siteSchedule: 24 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 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...

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...

Job Overview:Provide technical assistance as part of a team to develop and maintain clinical systems that meet internal and external clients needs. Assist with the development of third-party vendor data for local and central labs. Provide leadership to the Clinical Data Programming de More...

Please note this position is fully on-site with exposure to the sites in both Gilbert and Mesa Arizona. Join a collaborative patient-centered team where your contributions directly support groundbreaking studies and improved patient outcomes. This is more than just a CRC role its a u More...

Job OverviewServe as a relationship manager and strategic business partner responsible for expanding new business opportunities within their customer accounts.Essential FunctionsActively network in the industry to establish relationships and to identify potential opportunities.Establi More...

Job OverviewManage and support the operational elements and execution of studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction and in accordance with SOPs; policies and practices from pre-award to close-out. Wo More...

Job OverviewManage small to medium size Connected Devices that are stand-alone or full-service in scope across all clinical trial phases. With support from Senior Project Manager ensure all project work is completed to the sponsors satisfaction on time and within budget and in accorda More...

Job Overview:Acts as Lead Medical Writer on any type of writing project including projects with multiple deliverables/components. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Per More...

Job Title:Research AssistantWork Set-Up:Working On-siteScheduled Weekly Hours:32 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...

Job OverviewDevelop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors studies or multi-protocol programs as determined by the Sponsors requirements.Essential Functions Develop Coordinate the development of in More...

Clinical Specialist Consultant - 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 assessments are being conducted in a standard More...

Please note this position is fully on-site at the site in Springville Utah Join a collaborative patient-centered team where your contributions directly support groundbreaking studies and improved patient outcomes. This is more than just a CRC role its a unique opportunity to deepen y More...