Clinical Trials Coordinator

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,...

As a Clinical Trials Coordinator, you will be responsible for supporting clinical trial processes from feasibility studies to site initiation visits. You will work closely with healthcare professionals, patient advocacy groups, and key opinion leaders to ensure successful trial execution.

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...

Job OverviewSyneos Health, Inc. is a leading biopharmaceutical solutions organization that accelerates customer success through innovative clinical development models. Our team collaborates with passionate problem solvers to deliver therapies and change lives.About the RoleWe are seeking a highly organized and detail-oriented Clinical Trials Coordinator to...

We are seeking an experienced Clinical Operations Coordinator to join our team in supporting the delivery of clinical trials.This role requires strong organizational skills, attention to detail, and the ability to work effectively in a team environment.Bachelor's degree in a related fieldExperience in clinical operations or a related fieldAs a Clinical...

How You Will Succeed:As a Clinical Research Coordinator, you'll be responsible for supporting Investigator Site staff in conducting clinical research studies according to project-specific requirements and regulatory guidelines. Your key responsibilities will include:Monitoring Visits:Support organization and execution of monitoring visits and audits at the...

As a Study Start Up Associate at ICON plc, you will play a pivotal role in facilitating the initiation of clinical trials. This involves ensuring compliance with regulatory requirements and contributing to the advancement of innovative treatments and therapies.We are currently seeking a highly motivated and organized individual to join our diverse and...

Clinical Trial Project CoordinatorWe are seeking a skilled Clinical Trial Project Coordinator to join our team at Thermo Fisher Scientific. As a key member of our clinical operations team, you will be responsible for providing technical support to project teams, coordinating non-clinical responsibilities, and ensuring the smooth execution of clinical...

RequirementsTo be considered for this position, candidates must possess the following qualifications:At least one year of clinical trials monitoring experienceUniversity degree in life scienceExcellent written and oral communication skillsGood organizational and time management skillsFluent in written and verbal EnglishAbility to work well within a...

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...

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...

ICON Clinical Research Clinical Research Coordinator (Przemysl, Poland) in Warsaw, PolandClinical Research Coordinator - Przemysl, Poland - FTICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to...

Clinical Research Coordinator is a crucial role within the investigative site team, responsible for ensuring the success of clinical research studies according to project-specific requirements and regulatory guidelines.This position involves assisting in study-related activities at the site level, ensuring compliance with protocols, Standard Operational...

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...

Clinical Trials Administration ProfessionalWe're looking for a skilled Clinical Trials Administration Professional to join our team. As a key member of the Investigator Site team, you will be responsible for supporting staff in conducting clinical research studies according to project-specific requirements and regulatory guidelines.Your key responsibilities...

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...

**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...

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...

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,...

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...