Study Start Up Associate Ii

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...

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...

Regulatory Affairs, Study Start Up Specialist IICompany Overview:CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations.Job Description:This role involves assisting project teams with...

About the RoleWe are looking for a highly skilled Study Start Up Associate I to join our team. As a key member of our Site Activation Team, you will be responsible for supporting operational activities related to site evaluation, activation, initiation, monitoring, and close out for assigned investigator sites/studies.Your primary responsibilities will...

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...

About This OpportunityWe are excited to offer a challenging and rewarding career opportunity for a Study Start Up Associate I. As a key member of our team, you will have the opportunity to work on a wide range of projects, developing your skills and expertise in clinical trial management.Your responsibilities will include:Managing Study Site Activation:...

Job Title: Regulatory Affairs, Study Start Up Specialist IIJob Summary: We are seeking a highly skilled Regulatory Affairs, Study Start Up Specialist II to join our team.Key Responsibilities:Assist/advise project teams on all regulatory requirements for clinical studies.Perform compliance assessments according to country requirements and document any...

Regulatory Affairs, Study Start Up Specialist IIJob Overview:This role involves assisting project teams with regulatory requirements for clinical studies.Key Responsibilities:Advise project teams on all regulatory requirements for clinical studies.Perform compliance assessments according to country requirements and document any activity discovered; notify...

Job DescriptionClinical Trial SpecialistAs a Clinical Trial Specialist at Fortrea, you will play a crucial role in ensuring the success of our clinical trials. You will be responsible for reviewing Investigator Packages, developing Country initial ICFs, and assisting the study start-up teams with site start-up activities. Your attention to detail and ability...

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...

At Icon, we are committed to delivering quality and process improvement in our study start-up operations. As a Study Operations Specialist, you will play a crucial role in ensuring the success of our clinical trials by coordinating with study sites, sponsors, and internal personnel. Your key responsibilities will include:Key ResponsibilitiesCollecting,...

We currently have an exciting new opportunity for an Associate Project Manager to join our growing team, sponsor dedicated.The Associate Project Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clinical Operations, Study Management.This is a permanent role with ICON on FSP and fully...

Trial Activation Approval Specialist IKey Responsibilities:Submission Coordination: Prepares, reviews and coordinates EC submissions in alignment with global submission strategy under guidance.MoH Submission Support: Supports preparation of local MoH submissions, as applicable, under guidance, in alignment with global submission strategy.Site Start-up...

About ICONAt ICON, we are committed to delivering high-quality clinical trials that meet the needs of our clients. Our team of experts works closely with investigators and their teams to ensure timely and compliant study start-ups.We are seeking a talented Study Start Up Associate I to join our team. In this role, you will work closely with our clients to...

Location: Toluca, State of MexicoNumber of positions: 2**Position purpose**: As a CAPEX project team member, ensure vertical start-up and sustained performance by properly preparing and leading the start-up phase.**Required knowledge and experience**:Bachelor's degree in engineering or related fieldsAdvanced intermediate level of English2 to 3 years of...

Job Title: Regulatory Affairs, Study Start Up Specialist IIAbout Us:CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations.Key Responsibilities:Assist/advise project teams on all...

**Key Responsibilities**As a Clinical Trials Laboratory Manager at ICON, your key responsibilities will include:Managing laboratory-related activities for a project or a group of studies, including coordinating laboratory operations and ensuring compliance (ethical, legal, and regulatory) and quality to appropriate standards.Collaborating with Local Study...

About ICONICON is the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence. Our mission is to advance human health through innovative clinical research solutions.We're committed to providing high-quality services that meet the evolving needs of our clients. Our expertise spans a wide range of therapeutic...

Company OverviewFortrea is a leading global contract research organization that provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With decades of clinical development experience, Fortrea conducts operations in ~100...

At ICON plc, we're committed to fostering an inclusive environment that drives innovation and excellence. Our success depends on the quality of our people, which is why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.We're currently seeking a Senior Site Activation Lead to join our dynamic team. As a key...