Clinical Trial Coordinator

Job DescriptionThe Clinical Trial Project Coordinator Specialist will play a vital role in ensuring the smooth execution of clinical trials within our organization. This individual will be responsible for performing department, internal, country, and investigator file reviews as assigned, documenting findings in appropriate systems, and ensuring allocated...

Role SummaryICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence.We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning,...

As a key member of our team at CDS Fortrea Inc., you will serve as the primary contact for project teams and investigative sites, conducting site contacts and documenting interactions as required. Your responsibilities will include monitoring site performance, implementing action plans for underperforming sites, and assisting CRAs with site visit...

We are a dynamic and innovative company founded in 1995, with over 2,800 driven individuals worldwide.Our organization prioritizes the well-being of our staff, clients, partners, and the quality of our work. We are at the forefront of medical science, developing new medicines that change lives.As a key member of our international team, you will play a...

Are you a skilled biostatistician looking to advance your career in clinical trials?Job SummaryWe are seeking an experienced Lead Clinical Trial Biostatistician to join our team at Fortrea. In this role, you will be responsible for planning, executing, and overseeing all programming activities on studies, including resource estimation, working within budget,...

Unlock a World of Opportunities in Project CoordinationAbout Signant HealthSignant Health is a global leader in evidence generation, empowering customers to digitally enable their clinical trial programs. We connect with patients worldwide, driving innovation through technology and redefining the path to proof.As part of our team, you'll be at the heart of a...

Role Overview At Engineeringuk, we're seeking a highly skilled Clinical Trial Manager to lead the planning, execution, and successful completion of clinical trials. As a key member of our research team, you will be responsible for overseeing all aspects of clinical trials, ensuring adherence to timelines, budgets, and quality standards. This critical...

Clinical Trial Manager Role at ICON plcAt ICON plc, we're committed to delivering innovative healthcare solutions that make a difference in people's lives. As a world-leading clinical research organization, we're driven by a passion for excellence and a dedication to our clients.The role of Clinical Trial Manager at ICON plc offers an exciting opportunity to...

Key Responsibilities:• Perform department, internal, country, and investigator file reviews as assigned, documenting findings in the appropriate system.• Ensure allocated tasks are completed on time, within budget, and to a high-quality standard.• Proactively communicate any project risks to project leads.Supporting Study Operations:• Maintain...

Job DescriptionWe are seeking a Senior Medical Director to lead our clinical trials team. The successful candidate will have a strong background in pharmaceuticals and experience in managing clinical trials.ResponsibilitiesLead the development and implementation of clinical trial strategiesManage a team of medical professionals to ensure high-quality trial...

Overview">As a Clinical Research Project Coordinator at IQVIA, you will play a crucial role in ensuring the smooth execution of site activation activities. You will serve as the single point of contact for investigative sites, managing all aspects of project planning, timelines, and regulatory documents.">Responsibilities:">">Perform site startup and...

Job SummaryWe are seeking a highly skilled Regulatory Submissions Coordinator to join our team in Chile. As a key member of our Regulatory Submissions department, you will play a vital role in supporting the development of safe and effective medical therapeutics.Your primary responsibilities will include:Providing day-to-day support to our Regulatory...

OverviewICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence.Salary & BenefitsWe offer a competitive salary, estimated at $80,000 - $110,000 per year, depending on experience and qualifications. In addition to your salary, you can expect a...

Job DescriptionWe are seeking a highly experienced Clinical Trials Coordinator - Monitoring Specialist to join our team at ICON plc.About the RoleThis is an exciting opportunity for a seasoned professional to take on a key role in the set up and monitoring of clinical studies, ensuring compliance with applicable regulations and principles of ICH-GCP.The...

At ICON Plc, we're on a mission to shape the future of clinical development. As a Clinical Research Associate, you'll play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Job Description:We are seeking a skilled Clinical Research Associate...

About the Role:We are seeking a highly skilled and experienced Senior Clinical Research Coordinator to join our team at Thermo Fisher Scientific. This role will be responsible for coordinating clinical trials, ensuring timely completion of tasks, and maintaining high-quality standards.Key Responsibilities:Perform department, internal, country, and...

Job SummaryWe are seeking a seasoned Clinical Research Associate to join our team at ENGINEERINGUK. In this role, you will have the opportunity to work with cutting-edge clinical research projects and contribute to the advancement of healthcare.Key ResponsibilitiesMonitoring Activities: Conduct onsite and remote monitoring activities in accordance with...

Job Overview As a Clinical Research Associate at IQVIA, you will play a critical role in ensuring the successful execution of clinical trials. Your primary responsibility will be to conduct site monitoring visits to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations, and sponsor...

About ICON">ICON 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.Your Role">We are seeking a highly skilled Senior Clinical Research Physician Specialist...

Job OverviewAs a Clinical Research Associate at IQVIA, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of clinical trials. This includes performing site monitoring visits, adapting and driving subject recruitment plans, and managing ongoing project expectations and issues.Key...