Clinical Project Coordinator

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 OverviewWe are seeking a highly skilled Global Clinical Project Manager to join our team at SAN Fortrea Chile Limitada.

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 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...

Job SummaryA career opportunity has arisen within Medpace in Chile for a highly motivated and organized individual to join our Regulatory Submissions team as a Regulatory Submissions Coordinator. As a key member of the team, you will be responsible for providing day-to-day support activities, ensuring deadlines are met, and maintaining spreadsheets.This is...

About ICON PlcICON plc is a world-leading healthcare intelligence and clinical research organization. We pride ourselves on fostering an inclusive environment that drives innovation and excellence, making us a great place to grow your career.SalaryWe offer a competitive salary, estimated to be around $95,000 per year, depending on experience and...

We are seeking a highly skilled and experienced Key Project Coordinator to join our team at Michael Page. The successful candidate will be responsible for leading the organization of projects, ensuring that deliverables are met by each area involved.As a Key Project Coordinator, you will identify risks and mitigating factors during the project, support and...

Job OverviewWe are seeking a highly skilled Senior Wind Turbine Project Coordinator to join our team at Siemens Gamesa Renewable Energy, S.A.

Job OverviewWe are seeking a highly skilled and motivated Senior Technical Project Coordinator to join our team at Komatsu America Corp. This is an exciting opportunity for someone who wants to be part of a global leader in mine management technology.

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...

Job Description:GHD Group is seeking a meticulous and proactive Senior Project Coordinator to join our team.The successful candidate will play a crucial role in supporting project management activities, ensuring projects are set up, tracked, and closed out efficiently. This role demands excellent organizational skills, strong communication abilities, and a...

Thermo Fisher Scientific is seeking an experienced professional to support the supply chain for moderate complex global clinical trials. As a key member of our team, you will be responsible for ensuring project/study activities are in compliance with company and client requirements.You will act as a representative and project lead for the department on less...

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...

Job OverviewWe are seeking a highly skilled Clinical Research Coordinator to join our Regulatory Submissions team at Medpace in Chile.Estimated Salary Range:$60,000 - $80,000 per year, depending on experience.Key ResponsibilitiesProvide day-to-day support to Regulatory Submission Managers and Start Up teams, ensuring deadlines are met.Conduct quality control...

About the RoleWe are seeking a highly skilled and experienced Construction Project Coordinator to join our team at Turner & Townsend Group. As a key member of our project delivery team, you will play a critical role in ensuring the successful execution of mining projects.This is an excellent opportunity for a seasoned project professional to take on new...

About UsSAN Fortrea Chile Limitada is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience.We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20...

About VERIDAPTVERIDAPT is a pioneering tech company dedicated to making commodities more secure and sustainable. Our innovative hardware and software solutions provide real-time visibility into emissions, energy, agricultural, and metals commodities, enabling clients to track their progress, save money, and achieve net-zero targets.Job SummaryWe are seeking...

Job DescriptionWe are seeking a highly skilled Clinical Study Activation Specialist to join our team at ICON. As a key member of our organization, you will play a vital role in ensuring the successful activation of investigative sites for clinical studies.The ideal candidate will have a strong background in clinical research, with experience in managing...

Job DescriptionMSD is seeking a highly skilled Clinical Trial Monitoring Lead to oversee the clinical trial process and ensure seamless execution. As a key member of our team, you will be responsible for managing a team of 6-14 Clinical Research Associates (CRAs) and ensuring excellent study and site performance.Responsibilities:Work allocation, staff...

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...