QPL IQVIA RDS Poland

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...

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...

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 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...

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...

Associate Director Data Sciences Safety and Regulatory FSP SalesAssociate Director Data Sciences Safety and Regulatory FSP Sales will contribute to a major segment of the Sales organization FSP services for the Data Management Biostatistics Programming Medical Writing Lifecycle Safet 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...

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...

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...

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*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...

The IQVIA Internship provides you with the opportunity to gain relevant project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future.You will be wo More...

At IQVIA we are continuously expanding the boundaries of whats possible in clinical development through advanced analytics cutting-edge technology and deep scientific expertise. Within our Research & Development Solutions (RDS) organization we are enhancing our services with agent More...

IQVIA is The Human Data Science Company focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles IQVIA offers a broad range of solutions that harness advances in healthcare information More...

Join IQVIA as a CRA / SrCRA (m/w/d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing st More...

Join Our Team as a Therapeutic Strategy Lead!Are you passionate about creating innovative delivery strategies that meet customer needs Do you thrive in a collaborative environment where you can make a real impact If so we have the perfect opportunity for you!PurposeAs a Therapeutic St More...

The IQVIA Internship provides you with the opportunity to gain relevant project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future.You will be wo More...