Study Start-Up Coordinator

We're seeking a highly skilled Global Study Start-Up Specialist to join our team at myGwork. In this role, you'll contribute to the development and implementation of global clinical trials, with a focus on study start-up activities. This will involve working closely with cross-functional teams to ensure smooth trial execution and achieving high-quality...

Somos un holding mexicano con presencia global y con diversas líneas de negocio, pero con un fin en particular: PROCURAR LA SALUD Y EL BIENESTAR DEL SER HUMANO ÚNETE A NUESTRO EQUIPO DE TRABAJO CÓMO STUDY START UPEl Study Start Up es el responsable de coordinar y dar seguimiento a los procesos de inicio y cierre de los estudios clínicos, atracción de...

About the JobNovartis Farmacéutica is seeking a highly skilled Study Start-Up Expert to join our team. As a key member of our Study Start-Up department, you will be responsible for ensuring timely and efficient execution of trials and trial-related activities within budget and in compliance with quality standards.Key performance indicators include adherence...

At ICON, it's our people that set us apart.Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives.ICON plc is a world-leading healthcare intelligence and clinical research organization.From molecule to medicine, we advance clinical research by providing outsourced...

The Study Start Up.Assocate II, collect, prepare, review, approve, process and track regulatory and site level critical documents required for study site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable country regulations/guidelines and the principles of ICH/GCP.Embrace and contribute to ICON's culture of quality and process improvement...

About the RoleMajor accountabilities:Might be involved in various operational excellence activities like process improvement or other line function initiatives.Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt - Distribution of marketing samples (where applicable).Key...

About the Role Major accountabilities: Might be involved in various operational excellence activities like process improvement or other line function initiatives. Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt - Distribution of marketing samples (where applicable). Key...

This job is with Novartis, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Summary Contribuye, con una supervisión adecuada, a todos los...

About StudyWe're a culture-first organization dedicated to making a positive impact on education. Our team is passionate about learning and strives for excellence in everything we do.Company ValuesWe maintain a dynamic, start-up atmosphere where everyone works collaboratively and has a great time doing it. Our core values include being smart, friendly, and...

We're looking for a highly motivated and experienced Senior Clinical Trial Coordinator to join our team at myGwork. In this role, you'll provide coordination and administrative support for global clinical trials, with a focus on study start-up activities. This will involve working closely with investigators, sponsors, and other stakeholders to ensure...

About StudyWe're a forward-thinking organization revolutionizing the way people learn. Our team is passionate about education and strives for excellence in everything we do.Company CultureWe maintain a dynamic, start-up atmosphere where everyone works collaboratively and has a great time doing it. Our flat structure allows for quick decision-making and...

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.The role holder will contribute to best practices guidance or operational excellence activities to...

Centralized Study Specialist II Apply locations: Mexico City, Lima, San Jose, Buenos Aires, São PauloTime type: Full timePosted on: Posted 3 Days AgoTime left to apply: End Date: December 31, 2024 (4 days left to apply)Job requisition id: 2443695 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of...

QMT CoordinatorAs a QMT Coordinator, you will be enabling, developing and supporting suppliers with the industrialization and problem solving in series production, as well as defining and agreeing the reliability indicators/relevant critical characteristics to ensure quality standards.Furthermore, you will be guaranteeing the launch team integration with the...

Sr. SAL Overview: The Senior Site Activation Lead is accountable for the overall coordination, implementation, and completion of site activation activities for large global or complex projects of work in line with ICON/sponsor SOPs as appropriate. Key Tasks: Primary study start-up point of contact for designated complex and/or global projects. Developing...

We are looking for a highly skilled Global Clinical Operations Director to oversee global clinical operations and ensure their timely execution within budget and quality standards.About the JobThis position involves ensuring adherence to quality guidelines and regulations, and negotiating with key stakeholders.The successful candidate will have a minimum of...

We are looking for a skilled Clinical Trial Operations Manager to manage clinical trials and ensure their timely execution within budget and quality standards.About the JobThis position involves reporting technical complaints and adverse events related to Novartis products within 24 hours of receipt.The successful candidate will have a minimum of 5 years of...

Job OverviewWe are seeking a highly organized and detail-oriented Legal Assistant to join our Clinical Operations team at Medpace. In this role, you will play a key part in the start-up and management of clinical trials.Key Responsibilities:Contract Administration: Provide day-to-day support with general contract administrative duties;Document Preparation:...

As a Clinical Trials Laboratory Manager you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. Working in this program you will feel challenged...

You will need to login before you can apply for a job. Sector: Science and PharmaceuticalRole: ManagerContract Type: PermanentHours: Full Time As a Clinical Trials Laboratory Manager, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.You will be partnering with a pharmaceutical...