Clinical Trials Data Specialist

**About the Opportunity**We are seeking an experienced professional to join our team as a Clinical Trials Planning Specialist.The successful candidate will play a crucial role in operational strategy and planning within the pre-award space.The Clinical Trials Planning Specialist will be responsible for developing, analyzing, interpreting, and presenting...

Clinical Trials Support SpecialistWe are looking for a skilled Clinical Trials Support Specialist to support the clinical development of Alexion's pipeline at early phases of development.Main ObjectivesDevelop and maintain the highest scientific and medical expertise in the relevant fields.Closely collaborate with cross-functional teams to support clinical...

Clinical Trials Specialists at ICON plc play a crucial role in supporting the execution of clinical trials by collaborating with Investigator Site staff and Sponsor representatives.We're seeking a highly skilled and experienced individual to join our team as a Clinical Trials Specialist.This role involves coordinating study-related activities at the site...

Job DescriptionThe Clinical Data Scientist plays an integral part of our team here at Psi CRO Ag. This role involves working with clinical trials patient and operational data, developing new data solutions, and setting up Risk-based Monitoring systems in the Process Improvement department.Hybrid work in Warsaw allows for a great balance between work and...

We are seeking a highly skilled and motivated individual to join our team as a Clinical Trials Coordinator in Warsaw, Poland. As a Clinical Trials Coordinator, you will be responsible for providing administrative and logistical support to Clinical Trial Assistants, Site Managers, and Local Trial Managers in tracking progress of trials, managing study data,...

Job SummaryWe are seeking an experienced clinical research professional to join our team as a Remote Clinical Trials Manager.In this role, you will be responsible for managing clinical trials from start-up to close-out, ensuring compliance with regulatory requirements and study protocols.As a key member of our operations team, you will collaborate with...

Brief DescriptionThe Clinical Programmer will be responsible for the provision of data review and trial management deliverables across all compounds and trials for which these are required, and for all functional groups that require those deliverables.Essential Functions/ResponsibilitiesProgram simple to complex data review listings, exception reports,...

PrimeVigilance Ltd is a dynamic company that prioritizes diversity, equity, and inclusion. We create an equal opportunities workplace and a human-centric environment where people from all cultural backgrounds can contribute and grow.We're looking for a Clinical Trials Specialist who can work collaboratively with our project teams to deliver high-quality...

About the OpportunityWe are seeking an accomplished Clinical Trials Writer to join our team at GlaxoSmithKline. This role involves developing clinical trial documents and managing projects to ensure timely delivery of high-quality documents.Key Responsibilities:Clinical Trial Document Development: Develop and review clinical trial documents, including...

Our Company OverviewMedpace is a leading global clinical contract research organization (CRO). We offer a comprehensive range of services, from Phase I to Phase IV clinical trials, to support the development of innovative medical treatments.About UsWe have a long history of successfully delivering projects on time and within budget. Our expert team provides...

Company OverviewICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to advancing human health through innovation and excellence.We pride ourselves on fostering an inclusive environment that drives creativity, collaboration, and growth. As a Senior Global Regulatory Affairs Specialist, you will be part of a diverse...

Role OverviewThe Clinical Operations Specialist will play a critical role in the execution of clinical trials, focusing on financial management and logistics coordination.The successful candidate will have experience in a similar role within a pharmaceutical company or related field, with strong organizational and communication skills.Key...

Clinical Data Management at Merck GruppeWe are looking for a skilled Associate Director, Clinical Trials to lead our clinical data management activities. As a key member of our team, you will ensure the integrity and quality of clinical trial data.Your Responsibilities:You will oversee clinical data management activities, including planning timelines and...

Company Overview:We are a global healthcare company dedicated to accelerating medical innovation by making clinical trials more accessible and patient-friendly.Our mission is to bridge the gap between patients and doctors, ensuring seamless communication and timely access to life-changing treatments.Your Role:As a Clinical Trials Coordinator, you will be...

Company OverviewWe are a dynamic, global company that cares about our staff, clients, partners, and the quality of our work. With over 3000 dedicated individuals, we bring together passion, dedication, and expertise to change lives and bring new medicines to those who need them.Salary and BenefitsWe value your time and offer a competitive salary with...

Role OverviewWe are seeking a highly skilled Monitoring Clinical Trials professional to join our team in Warsaw, Poland. As a Sponsor Dedicated CRA, you will play a crucial role in the success of our clinical trials, working closely with study site teams and client representatives to ensure compliance with regulatory requirements.Your responsibilities will...

We're looking for a talented Clinical Trials Proposal Manager to join our team at TN Poland. As a key member of our proposal development team, you will contribute to producing high-quality proposals that resonate with clients.Role OverviewThe successful candidate will be responsible for developing and coordinating all phases of proposal development, from RFP...

Job Title: Clinical Research AssociateDescription:We are looking for a highly motivated and experienced Clinical Research Associate to join our team at IQVIA Biotech. As a Clinical Research Associate, you will be responsible for ensuring the successful conduct of clinical trials by performing monitoring and site management work.Key Accountabilities:The key...

Social network you want to login/join with:SAS Programmer in Clinical Trials, WarsawClient:PSI CROLocation:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:8ba4836cfbf6Job Views:3Posted:24.03.2025Expiry Date:08.05.2025Job Description:Actual position's title: Clinical Data ScientistReporting to the Clinical Data Science Manager and...

Social network you want to login/join with:Clinical Data Manager / Senior Clinical Data Manager - Europe - Office or Home Based, WarsawClient: Worldwide Clinical TrialsLocation: Warsaw, PolandJob Category: OtherEU work permit required: YesJob Reference: 4349b59d5f07Job Views: 55Posted: 23.01.2025Expiry Date: 09.03.2025Job Description:Requisition Number:...