Clinical Trials Statistician

We are seeking a highly skilled Data Science Statistician to join our team at IQVIA Argentina.About the Role:The successful candidate will be responsible for utilizing SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. This role requires strong analytical skills,...

Job Title: Clinical Data ProgrammerEstimated Salary: $80,000 - $110,000 per year.About the Role:We are seeking a skilled Clinical Data Programmer to join our team at IQVIA Argentina. As a key member of our clinical research services group, you will be responsible for utilizing the SAS programming language to develop clinical study report materials according...

About the OpportunityWe are excited to offer an exceptional opportunity for a skilled Pharmacy Operations Specialist Clinical Trials to join our team at Royal Berkshire NHS Foundation Trust. As a key member of our dispensary team, you will play a crucial role in the management of clinical trials, working closely with our clinical trials pharmacist,...

Clinical trials coordinators play a vital role in ensuring the success of clinical trials at ICON. As a senior proposal developer, you will be responsible for developing and coordinating proposals and budgets for new business opportunities.About the CompanyICON is a world-leading healthcare intelligence and clinical research organization. We pride ourselves...

About the PositionWe are seeking an experienced Dispensary Clinical Trials Team Manager to join our team at Royal Berkshire NHS Foundation Trust. This is an exciting opportunity for a skilled professional to take on a leadership role, overseeing the management of clinical trials within our dispensary.Job SummaryThe successful candidate will be responsible...

The IQVIA Global Site Activation team is a market leader in Clinical Trial Site Activation, delivering exceptional employee, site, and customer experiences. As a Clinical Trial Activation Specialist, you will oversee the Start-Up phase, designing and implementing our strategy towards site activation from award to open enrollment. You will also lead our...

Clinical Research Administrator Role at ICON plcEngineer clinical trials to shape the future of healthcare with us.About UsWe are a leading provider of healthcare intelligence and clinical research services. Our mission is to foster an inclusive environment driving innovation and excellence, while delivering exceptional results for our clients.The...

ICON plc is seeking a highly skilled Lead Statistician for Data Analysis to join our team in Reading, UK.About the OpportunityThe salary for this role is £80,000 - £110,000 per annum, depending on experience. Our company offers a comprehensive benefits package that includes various annual leave entitlements, a range of health insurance offerings, and...

We are currently seeking a Clinical Trials Coordinator Lead to join our team in the South West of England. In this role, you will be responsible for managing the progress of assigned studies, tracking regulatory submissions and approvals, and resolving data queries.About IQVIAIQVIA is a global leader in clinical research services, commercial insights, and...

Clinical Research Associate Role OverviewWe are seeking a skilled Clinical Research Associate to join our team and provide site monitoring services for our clients. This role involves working closely with sites across Northern England and Scotland to ensure the successful execution of clinical trials.Key Responsibilities:Conduct site monitoring visits to...

Job DescriptionThe ideal candidate for this position will have 7 years of experience in clinical trials, with a strong background in managing coding and data management processes for multiple global projects. The role requires excellent knowledge of medical dictionaries, medical terminology, pharmacology, anatomy, and physiology. Additionally, the candidate...

IQVIA LLC seeks a highly skilled Clinical Research Associate to join its team in the South West of England. As a key member of our sponsor-dedicated team, you will be responsible for supporting sites across the region and ensuring the successful execution of clinical trials.Your primary duties will include conducting site monitoring visits, working with...

About Clinical Trials Programmer II Role\At ICON plc, we are seeking an experienced Clinical Trials Programmer II to join our global biostatistics team, working on late-phase research projects. As a key member of our team, you will be responsible for statistical aspects of clinical and preclinical research projects, including study design, case report form...

At ICON plc, we are looking for a talented Lead Clinical Trials Data Specialist to contribute to our mission shaping the future of clinical development. As a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries, we welcome applications from across EMEA.Job OverviewThis role plays a...

**Job Description**As a Clinical Trials Developer at Warman O'Brien, you will play a crucial role in driving innovation and advancing patient care. You will be responsible for designing systems for seamless data access, analysis, and reporting, as well as guiding junior programmers within the team.To succeed in this role, you will need to possess a...

Job SummaryWe are seeking an experienced Statistical Analysis Director to join our team at ICON plc. In this role, you will be responsible for leading the statistical analysis of clinical data and providing strategic guidance to support decision-making and reporting.About the Role:Developing and implementing statistical analysis plans for clinical trials,...

ICON plc is a world-leading healthcare intelligence and clinical research organization, headquartered in the UK.We are currently seeking a Clinical Research Associate to join our dynamic team. This role involves overseeing and coordinating clinical trials, ensuring compliance with regulations and collecting critical data.Job Summary:This is a full-time...

Product Visionary - Enterprise SaaS SoftwareAbout the Job DescriptionAs a key member of our team, you will be responsible for driving innovation in clinical trials labelling, medical devices, and life sciences within a dynamic enterprise SaaS environment.About the RequirementsTo succeed in this role, you will need:5+ years of experience in product...

Job OverviewIQVIA, Inc. is seeking a highly skilled SAS Programmer to join our team. As a senior member of our clinical study report development team, you will be responsible for creating high-quality clinical study reports using your programming expertise.Key Responsibilities:Importing and Validating Data: Import data from various sources and perform...

Job DescriptionWe are seeking a highly skilled Clinical Data Management Lead to join our team at IQVIA Argentina. As a key member of our clinical data management team, you will be responsible for performing scientific clinical data review in close collaboration with Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS).Your primary...