Cra Manager

CRA Line Manager **Category**:Clinical Development**Location**:Ciudad de México, Ciudad de México, MX- **Position Description** As a CRA Line Manager at Novo Nordisk, you will: - Manage a team of CRAs to ensure compliance with ICH/GCP, SOPs, and local regulations. - Oversee resource allocation and monitor staff utilization for clinical projects in the...

Site relationship management role to ensure sustainable trial start-up at Site. The Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I-IV GDD trials within the country in adherence with monitoring procedures and processes in accordance with ICH/GCP, local...

Labcorp Drug Development is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. Are you ready for the next step in your career? We are currently recruiting for a Clinical Research Associate I in Mexico. Role description: - Ensure the study staff who will conduct the protocol have...

**Description** **CRA II or Sr CRA oncology & on site experience Home Based Mexico** **CDMX/Aguascalientes/Oaxaca/Guadalajara - availability to travel required** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting...

IQVIA Biotech is committed and dedicated to the small biotech & biopharma companies we support. Opportunities available for an experienced Clinical Trial Manager II or Senior Clinical Trial Manager. Previous clinical trial management and CRO experience preferred. Therapeutic requirements/preference: any of the following Oncology/Hematology/CAR T/Cell &...

**Description** **CRA II or SR CRA assigned to client CDMX/GDL/MTY** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide...

The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning, executing and reporting, (from first site initiation visit to and including study site close-out), of assigned Global Drug Development (GDD) studies in compliance with Novartis processes and regulatory requirements. The CPM is the single point of contact and study team lead,...

**Job Description**: The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, policies and procedures, quality standards and adverse event reporting requirements internally and...

PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. Our global...

Job Title: Lead CRAAbout the RoleWe are seeking a highly skilled and experienced Lead Clinical Research Associate to join our team at PSI. As a Lead CRA, you will play a key role in managing local Monitors, supervising clinical monitoring and site management activities to ensure the protection of trial subjects' rights, safety, and well-being, data quality,...

392018BR **Clinical Project Manager**: Mexico **About the role** **Work Model**:Hybrid **Locality**:Ciudad de Mexico **About the Role**: The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning, executing and reporting, (from first site initiation visit to and including study site close-out), of assigned Global Drug Development...

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary...

Job Overview">We are seeking an experienced Clinical Research Project Manager to join our team in a leadership role. As a member of the PSI team, you will be responsible for managing local Monitors, supervising clinical monitoring and site management activities to ensure the protection of trial subjects' rights, safety and well-being, data quality and study...

En BASF, estamos comprometidos con la inclusión, proporcionando siempre que sea posible, ajustes razonables a las personas con discapacidad o con alguna necesidad específica, para garantizar su acceso y el uso de servicios. En caso de requerir algún apoyo, favor de comunicarlo durante tu primer contacto con Atracción de Talento. Estamos buscando...

Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Study Start-Up Manager (Regulatory Submissions Manager) to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position plays a key role in the clinical trial management process at Medpace. If you want an...

Job Description:In this key role, you will oversee local monitoring teams, supervising clinical monitoring and site management activities to ensure the integrity of trial data and compliance with regulations.Key Responsibilities:Lead regional projects as a senior member of the monitoring team, overseeing study activities, timelines, and schedulesTrain and...

This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Head COMs, the person is responsible for execution and...

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,...

Are you passionate about clinical research and leadership? We are looking for a new CRA Line Manager to join our team in the CMRQ department, supporting the obesity team at Novo Nordisk. If that sounds like you, read on to learn more about this exciting opportunity.Key ResponsibilitiesManage a team of CRAs to ensure compliance with ICH/GCP, SOPs, and local...

- - COVID-19 Vaccination Update for U.S. & Canada Colleagues All U.S. colleagues are required to disclose their COVID-19 vaccination status. New hires will be asked to disclose their vaccination status upon the first day of employment. - U.S. new hires (including those in Field Sales, Field Services and Customer Support - Technical Applications) may be...