Regulatory Submissions Coordinator

Job SummaryMedpace, a full-service clinical contract research organization (CRO), offers an exciting opportunity as a Regulatory Submissions Coordinator. This role supports our many projects and provides vital experience in clinical research.Responsibilities:Provide day-to-day departmental/project support activities, such as collecting vital documents for...

About GuerbetGuerbet is a global leader in medical imaging, offering a comprehensive portfolio of pharmaceuticals, medical devices, digital, and AI solutions for diagnostic and interventional imaging. With a rich history of innovation, we continuously push the boundaries of medical imaging to improve patient outcomes.Job SummaryWe are seeking a highly...

About the RoleAs a Regulatory Affairs Coordinator for Guerbet in Chile, you will play a crucial role in ensuring the timely completion and filing of regulatory submissions for medical devices and pharmaceuticals products. This position requires a strong understanding of the regulatory strategy of the company and the ability to manage regulatory submissions...

Job Description:We are seeking a skilled Clinical Research Coordinator to support our Regulatory Submissions team in Chile.Responsibilities:Provide day-to-day support for regulatory submissions, including document collection and preparation.Collaborate with Regulatory Submission Managers and Start Up teams to ensure timely completion of tasks.Conduct quality...

At Guerbet, we build lasting relationships to enable people to live better. This is Our Purpose.We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging.As a pioneer in the field of contrast products since 95 years, we continuously...

Job SummaryWe are seeking a skilled Regulatory Affairs Specialist to join our team at Pfizer.This role will support the Regulatory team in new product registration and post-approval changes, working closely with local and regional stakeholders to deliver efficient regulatory submissions and processes.The successful candidate will possess a thorough...

Job SummaryPfizer seeks a skilled Regulatory Science Analyst to support the Regulatory team in new product registration and post-approval changes.Support regulatory submissions and processes, collaborating with local and regional teams.Familiarize yourself with latest changes in BoH legislation and local market requirements.This role requires a thorough...

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...

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...

CVS Health is committed to delivering enhanced human-centric healthcare for a rapidly changing world.Salary: $45,000 - $60,000 per year, depending on experience.About the JobThis role requires working from an existing CVS HealthHUB location in the Wellness room. The Retail Health Coordinator will communicate with plan and retail health identified members...

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...

Retail Health Services CoordinatorWe are seeking a highly motivated and detail-oriented Retail Health Services Coordinator to join our team at CVS Health in Valparaiso, IN.This role will require you to work from an existing CVS HealthHUB location within the Wellness room. Under the remote supervision of a clinical operation leader and local leader, you will...

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...

Job SummaryAs a Clinical Trial Coordinator at Thermo Fisher Scientific, you will play a vital role in ensuring the smooth operation of clinical trials. Your primary responsibility will be to perform department, internal, country, and investigator file reviews as assigned and document findings in the appropriate system. You will also be responsible for...

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...

Job DescriptionA competitive salary of $65,000 per year awaits a highly skilled Clinical Study Activation Specialist to join our dynamic team at EngineeringUK.About the Role:We are seeking an experienced professional to manage start-up activities for assigned studies at the regional level. This includes supporting site identification/site recruitment/site...

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.We offer a competitive salary package with an estimated $80,000 per year.Job Description:This role is an ideal stepping-stone for career progression in clinical research. You will receive training and development...

Job OverviewClinical research associates play a critical role in ensuring the quality and integrity of clinical trials. As a site manager, you will be responsible for conducting monitoring visits to ensure that sites are conducting studies and reporting data as required.Essential FunctionsPerform site monitoring visits in accordance with contracted scope of...

Unlock a fulfilling career in clinical research with IQVIA, a global leader in advanced analytics, technology solutions and clinical research services. As a Clinical Research Associate, you will play a critical role in the planning and execution of global projects, working closely with a dynamic team of professionals.Key ResponsibilitiesPerform site...

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...