iqvia

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenanc المزيد...

We are looking for a talented & highly motivated fresh graduate candidates to gain firsthand experience in the field of Clinical Research. During the internship you will become a valuable member of our clinical team by contributing to individual projects aimed to develop your care المزيد...

As a Senior PV Agreements Specialist you will develop and prepare pharmacovigilance agreements for assigned customer. Main Responsibilities: Work closely with project teams to determine appropriate terms and conditions of safety agreements. Develop and prepare safety agreements. Prima المزيد...

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department issupporting our clients project team in the execution of clinical the team provides the opportunity to work with the preparation and documentation of clinical research projects in differen المزيد...

To be eligible for this position you must reside in the same country where the job is located.The IQVIA Market Access Strategy Consulting team (formerly known as Amundsen Consulting) is a market-leading strategy and analytics division within IQVIA that helps manufacturers in the pharm المزيد...

Job OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budget and resources.Home Based role which will require yearly المزيد...

Deliver high quality coordination of the centralized support by the document service management group for upload of relevant Clinical Pharmacology & Pharmacometrics (CPP) documents (e.g. population PK/PD data transfer plans population PK/PD analysis plans and population PK/PD repo المزيد...

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company. If so come and join us - IQVIA are looking for a Clinical Research Coordinator.This part-time role is to support a site in Halifax West Yorkshire in conducting a clinical trial المزيد...

Are you an experienced nurse with expertise in womens health Do you excel in providing high-quality womens health services including the fitting and removal of coils in a supportive and professional primary care environment If so wed love to hear from you!We are seeking a passionate a المزيد...

Experienced CRA - SwedenJob OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Perform site المزيد...

Are you an experienced nurse with expertise in administering IVT Injections If so wed love to hear from you!We are seeking a passionate and skilled Ophthalmic Nurse Injectors to join our Healthcare Professionals Network in London.Essential Experience Needed: Good communication skillsE المزيد...

IQVIA Safety Operations team play an important part in the design build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international diverse team based across the world with safety المزيد...

Senior Business Systems Analyst (Remote)IQVIA Laboratories IQVIA Laboratories is a global leader in drug discovery and development offering comprehensive central and specialty biomarker services. Our expertise includes genomics immunoassays flow cytometry anatomic pathology precision المزيد...

To ensure work is completed in a timely and high-quality fashion on all validation outsource and audit projects. To ensure the appropriate resources are deployed for work on client engagements in order to facilitate a positive and productive long-term relationship.Essential FunctionsA المزيد...

Join IQVIA as a Senior Clinical Research Associate I / Sr CRA 1 (m/w/d) home-based throughout Germany in our single sponsor department and advance your career in clinical research. Youll enjoy the stability and resources of a leading global contract research organization while gaining المزيد...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenanc المزيد...

The Associate Principal Statistical Programmer will be responsible for review datasets in submission ready standard format (ADaM) tables figures listings and submission packages. This individual will provide expertise in the design development and quality control process for SAS progr المزيد...

TDM services provide for the regional/global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure regional/global clinical operations deliverables progress according to agre المزيد...

Are you looking for an opportunity to work with an industry-leading company IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Venice Mestre.This role with an immediate start is for 24 hours per week and is expected to last around one year. The succ المزيد...

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 المزيد...