Start Up Associate

Ensure that all assigned maintenance and Start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality and applicable laws and guidelines - Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner - With guidance from line manager and experienced colleagues,...

Job Summary:  The jobholder, an SME for local/regional regulations, works with multiple vendors, drives and coordinates activities across a range of stakeholders in support of site start up delivery.  This role liaises with Covance Regulatory to ensure compliance, coordinates best practice solutions within region and coaches others in the more complex...

Study Start Up Associate I - Contracts & budgets - Mexico - Homebased 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 We are currently seeking a...

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...

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 fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

Study Start Up Associate (All levels: I, II and Sr) - Remote - Mexico 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 We are currently seeking a...

Study Start Up Associate I - Site Activation Associate I - Mexico - Remote 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 At ICON, it’s our...

Novartis Farmacéutica is seeking an experienced Study Start-Up Coordinator to join our team.About the RoleThis position involves managing cross-functional collaboration, operations management and execution, and critical negotiations.The successful candidate will have a strong background in clinical research positions, specifically in Study Start-Up.Project...

Study Start Up Associate I (Regulatory Submissions) Mexico City - Hybrid Scheme 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 We are currently...

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...

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...

Completed job training (office management, administration, finance, health care preferred) or Bachelor’s Degree. Ideally an accountant by profession or with extensive experience in payments and financial processes. - Minimum 1-2Y in Clinical Research or relevant healthcare experience **Labcorp is proud to be an Equal Opportunity Employer**: As an EOE/AA...

**Labcorp is proud to be an Equal Opportunity Employer**: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data,...

**Labcorp is proud to be an Equal Opportunity Employer**: As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race,...

Collect, track and perform a quality review of all essential & investigator documents required for effective and compliant study site activation and maintenance - Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner. - Proactively manage sites to ensure timely site activation and escalate study...

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 fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

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...

You will join an international team dedicated to support all types of clinical trials at the start up as during the course of the study. Main tasks consist of document review: - Review Initial Greenlight Packages to assure compliance with regulatory requirements before granting regulatory green light to a site to start enrolling patients into the clinical...

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...