Senior Clinical Study Start Up Specialist

At ICON plc, we're committed to advancing and improving patients' lives through our work in clinical research. As a member of our Study Start Up Team, you'll play a vital role in ensuring that our research sites are prepared to start clinical trials of new pharmaceutical and biological products.The Study Start Up Team is responsible for coordinating and...

Study Start Up Associate IIAt ICON Plc, our team enables us to advance and improve patients' lives by becoming a better partner to our clients.We're driven by four key values: Accountability & Delivery, Collaboration, Partnership, and Integrity. We aim to deliver excellence to our clients and patients at every touch-point.In this role, you will play a...

We are seeking a highly skilled Clinical Trial Start-Up Specialist to join our team at ICON. As a key member of our team, you will be responsible for advancing clinical trial start-up activities by understanding client objectives and assisting in the development of plans for country and site distribution.The ideal candidate will have a strong background in...

Job Title: Regulatory Affairs SpecialistAbout the Role:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Intrials Clinical Research. As a Regulatory Affairs Specialist, you will be responsible for managing regulatory and start-up activities for clinical trials in Latin America.Key Responsibilities:- Manage regulatory and...

Job Title: Senior Study Start-Up SpecialistBeiGene is seeking a highly skilled Senior Study Start-Up Specialist to join our team. As a key member of our clinical operations team, you will be responsible for delivering study start-up, initial and ongoing submissions within established timelines with high quality and in accordance with ICH/GCP, BeiGene SOPs,...

Job Summary:We are seeking a highly skilled and experienced Clinical Trial Management Associate to join our team in a Senior Regional Clinical Trial Management Associate role.About the Role:As a Senior Regional Clinical Trial Management Associate, you will be responsible for supporting the Regional Clinical Study Manager in regional study delivery and...

We are seeking a Clinical Trial Start-Up Specialist to advance clinical trial start-up activities by understanding client objectives and assisting in the development of the plan for country and site distribution.The ideal candidate will have a strong understanding of regulatory and submission processes in various countries and excellent written and verbal...

Job SummaryMedpace, Inc. is seeking a highly skilled Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo. This role plays a critical part in the clinical trial management process, requiring a strong understanding of regulatory requirements and a proactive approach to issue resolution.ResponsibilitiesManage and execute global start-up...

Job Title: Study Start Up Associate IAs a Study Start Up Associate I, you will play a key role in accelerating the development of our customers' drugs and devices through innovative solutions. You will be dedicated to one of our clients, embedded in their working environment, systems, and processes.Key Responsibilities:Perform investigator recruitment...

Job Title: Study Start Up Associate IAs a Study Start Up Associate I, you will play a pivotal role in accelerating the development of our customers' drugs and devices through innovative solutions. You will be a dedicated resource to one of our clients, embedded in their working environment, systems, and processes. Your responsibilities will include writing...

Principal Clinical Research AssociateJob SummaryCTI Clinical Trial Services, Inc. is seeking a highly skilled and experienced Principal Clinical Research Associate to join our team. As a key member of our clinical operations team, you will be responsible for overseeing the management of clinical trials, ensuring compliance with regulatory requirements, and...

Job Title: Regulatory Affairs At Intrials Clinical Research, we are seeking a highly skilled and experienced Regulatory Affairs professional to join our team.Primary Responsibilities:Manage the Regulatory & Study Start-up team in all aspects, with support from the Regulatory and Study Start-up Manager (RSM).Support RSM in defining metrics and KPIs for the...

Site Activation LeadICON 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 shape the future of clinical development.About the RoleWe are currently seeking a Site Activation Lead to join our diverse...

Job SummaryBoston Scientific is seeking a highly skilled and motivated Clinical Specialist to join our team. As a Clinical Specialist, you will be responsible for providing clinical support to customers, including troubleshooting, programming, and patient follow-up for our medical devices.Key ResponsibilitiesProvide clinical support to customers, including...

Job Title: Study Start Up Associate IAs a Study Start Up Associate I at ICON Strategic Solutions, you will play a pivotal role in accelerating the development of our customers' drugs and devices through innovative solutions.You will be dedicated to one of our clients, embedded in their working environment, systems, and processes. Your responsibilities will...

Job Title: Senior Director for Clinical StudyAt SINOVAC BIOTECH LTD., we are seeking a highly experienced Senior Director for Clinical Study to lead our clinical development strategy and medical affairs efforts in oncology and cell therapy.Key Responsibilities:Develop and implement comprehensive clinical development strategies for cancer therapeutics.Lead...

Job Title: Regional Clinical Study ManagerBeiGene is seeking a highly motivated and experienced Regional Clinical Study Manager to join our team. As a key member of our clinical operations team, you will be responsible for leading the regional clinical operations team and ensuring the successful delivery of clinical studies in the region.Key...

Key Responsibilities:As a Clinical Research Associate Lead at CTI Clinical Trial Services, Inc, you will serve as the main point of contact for assigned study sites, conducting site visits and completing site visit deliverables with quality and within given timelines. You will also assist with or oversee study start-up activities, including feasibility,...

Job SummaryWe are seeking a highly experienced Principal Clinical Research Associate to join our team at CTI Clinical Trial Services, Inc. As a key member of our site management team, you will be responsible for ensuring the successful execution of clinical trials at assigned study sites.Key ResponsibilitiesServe as the primary point of contact for assigned...

Senior Manager, Study Site EngagementAbout the RoleWe are seeking a highly skilled and experienced Senior Manager, Study Site Engagement to join our team at Takeda Pharmaceutical. As a key member of our clinical research team, you will be responsible for establishing and maintaining effective partnerships between Takeda study teams, study sites, and Clinical...