Clinical Trials Senior Analyst

Are you passionate about clinical trials and ensuring compliance with regulations? We are seeking a skilled Clinical Trials Senior Analyst to join our team at Novo Nordisk A/S in Mexico.The PositionAs a Clinical Trials Senior Analyst, you will be responsible for:Coordinating with importers, couriers, and customs agents to ensure compliance with importation...

About the RoleWe are seeking a highly skilled Clinical Trials Senior Analyst to join our team in Mexico. As a key member of our clinical development team, you will play a critical role in ensuring the successful execution of clinical trials.Key ResponsibilitiesDevelop and maintain strong relationships with importers, couriers, and customs agents to ensure...

Job OverviewAs a key member of our team, you will be responsible for ensuring the smooth start-up and maintenance of clinical trials in assigned countries. This includes coordinating with investigative sites, collecting and organizing required documents, and interacting with regulatory authorities to ensure compliance with applicable regulations and...

Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled and experienced Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical trials team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local regulations.Key...

{"title": "Clinical Trials Project Manager", "content": "Job OverviewAs a Clinical Trials Project Manager at IQVIA, you will lead and oversee the execution of clinical projects and research studies in accordance with global and local regulations to best meet customer needs while working toward organizational goals and strategies.Key Responsibilities:Provide...

Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local regulations.Key...

Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local regulations.Key...

Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled and experienced Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local...

Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled and experienced Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local...

Job Title: Sr. Clinical Trials AssistantJob Summary:We are seeking a highly skilled Sr. Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local regulations.Key...

{"Job Overview": "As a Sr. Clinical Trials Assistant at IQVIA, you will play a key role in leading and overseeing the execution of clinical projects and research studies. Your expertise will ensure compliance with global and local regulations, meeting quality and timeline metrics, and providing project-related support to project management...

Contract Analyst II Role at ICONICON 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 be a part of our mission to shape the future of clinical development.We are currently seeking a Contract Analyst II to join our diverse...

Job OverviewAs a leading global contract research organization (CRO), Fortrea is seeking a highly motivated and detail-oriented Clinical Trials Specialist to join our team. In this role, you will be responsible for coordinating and collecting data and information required by regulatory authorities, including the preparation of study documentation and...

Job SummaryWe are seeking a highly skilled Clinical Trials Project Manager to join our team at IQVIA. As a key member of our clinical research team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local regulations.Key ResponsibilitiesProvide project-related support to...

Position OverviewWe are seeking a highly skilled and experienced Clinical Trials Coordinator to join our team at Novo Nordisk. As a key member of our Clinical Data Science and Evidence team, you will play a pivotal role in managing clinical and real-world evidence studies.Key ResponsibilitiesOversee the lifecycle management of clinical and real-world...

Job Title: Senior Regulatory Affairs Specialist with Experience in Clinical TrialsAt ICON Plc, we're committed to fostering an inclusive environment that drives innovation and excellence. We're seeking a highly skilled Senior Regulatory Affairs Specialist to join our team.Key Responsibilities:Lead the preparation, submission, and maintenance of regulatory...

Senior Regulatory Affairs Specialist with Experience in Clinical Trials At ICON Plc, we're seeking a highly skilled Senior Regulatory Affairs Specialist to join our team. This role will be responsible for leading the preparation, submission, and maintenance of regulatory documents for clinical trials. Key Responsibilities: Develop and implement regulatory...

Job Title: Senior Regulatory Affairs Specialist with Experience in Clinical TrialsAt ICON plc, we're seeking a highly skilled Senior Regulatory Affairs Specialist to join our dynamic team. As a key member of our regulatory affairs team, you will play a pivotal role in ensuring regulatory compliance and facilitating the successful execution of clinical...

{"Job Overview": "Lead Clinical Trials OperationsAs a key member of our team, you will be responsible for leading clinical trials operations, ensuring the delivery of high-quality results to our clients. You will work closely with project and clinical leads to achieve project objectives, while optimizing speed, quality, and cost of delivery.Key...

Job Title: Clinical Trials Quality Assurance AuditorWe are seeking a highly skilled Clinical Trials Quality Assurance Auditor to join our team at PSI CRO. As a Clinical Trials Quality Assurance Auditor, you will play a critical role in ensuring the high quality of our clinical trials and internal company processes.Key Responsibilities:Conducting and...