18 publicaciones de empleo destacadas de patient safety en ciudad de méxico (¡Están contratando!)

Senior Site Navigator
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Bachillerato
- Licenciatura
Production Supervisor II
Airgas —Industrial, CDMX
- $85,000 por año
- Tiempo completo
- Bachillerato
- Licenciatura
- Seguro dental
- Permiso de maternidad y paternidad
Clinical Research Physician
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Doctorado
- Inglés
- Microsoft Office
- Seguro dental
- Seguro de la vista
3d
Operation Room Nurse
Power IVF —Roma Norte, CDMX
- $25,000 a $35,000 por mes
- Tiempo completo
- Enfermería
- Inglés
- Licenciatura
Postulación rápida
Medical Director
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Seguro dental
- Seguro de la vista
10d
Life Sciences R&D Consultant/Manager
Accenture —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Maestría
Local Clinical Project Manager
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Licenciatura
Post Market Complaints Data Analyst
Convatec —Nápoles, CDMX
- Tiempo completo
- Microsoft Excel
- Azure
- Administración de personal
13d
Principal Clinical Scientist
Precision Medicine Group —Ciudad de México, CDMX
- Home Office (Desde casa)
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Production Operator V
Airgas —Industrial, CDMX
- $32 a $40 por hora
- Tiempo completo
- Servicio al cliente
- Bachillerato
- Seguro dental
- Permiso de maternidad y paternidad
14d
Nurse
POWER FERTILITY CLINIC —Roma Norte, CDMX
- $10,000 a $30,000 por mes
- Tiempo completo
- Enfermería
- Inglés
- Licenciatura
Postulación rápida
DD&T, Instructional Designer (Sr.), Digital Dexterity
Takeda Pharmaceutical —Cuajimalpa, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Microsoft Office
- Seguro dental
- Seguro de la vista
EHSS Platform Engineer
Takeda Pharmaceutical —Cuajimalpa, CDMX
- Tiempo completo
- Administración de personal
- Informática
- Inglés
- Seguro dental
- Seguro de la vista
Key Account Manager
Theramex —Ciudad de México, CDMX
- Mercadotecnia
- Inglés
- Microsoft Office
Nurse
Power IVF —Roma Norte, CDMX
- $15,000 a $30,000 por mes
- Tiempo completo
- Enfermería
- Inglés
- Licenciatura
Postulación rápida
Senior Embryologist (Bilingual Chinese & Spanish)
POWER IVF CLINIC —Roma Norte, CDMX
- $25,000 a $60,000 por mes
- Tiempo completo
- Bilingüe
- Inglés
- Maestría
Postulación rápida
IT Support Engineer
Theramex —Ciudad de México, CDMX
- Azure
- Administración de personal
- Informática
AI / ML Engineer
Solventum —Ciudad de México, CDMX
- Tiempo completo
- Azure
- Informática
- Inglés

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Production Supervisor II
Airgas —Industrial, CDMX
Experience leading teams in a production environment. Experience and working knowledge of cylinder fill operations or similar industrial production industry.
$85,000 por año

Quiero recibir la alerta de empleo más reciente para patient safety en ciudad de méxico

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Senior Site Navigator

Fortrea -
Ciudad de México, CDMX

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Información del empleo

Tiempo completo

Cualificaciones

Inglés
Bachillerato
Licenciatura
Capacitación
Contratos

Descripción completa del empleo

Job Overview:

Senior Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites, this role ensures smooth progression from feasibility and initial outreach through to site activation, extending through the maintenance phase of the study as required. A crucial component in meeting the requirements of the Senior Site Navigator role is ensuring regulatory compliance, robust site management, optimal site support and training, and effective collaboration between the sponsor, CRO, and clinical site staff.

The Senior Site Navigator serves as local country expert in study start-up activities for a particular country or region. As senior team members, they perform work with limited oversight and their responsibilities include acting as a “knowledge resource,” mentoring /training junior colleagues if suitable. The Senior Site Navigator proactively anticipates and mitigates issues that could delay the study.

Summary of Responsibilities:

Oversight of site level tasks associated with efficient site activation in accordance with ICH/GCP guidelines, local regulations, SOPs and project requirements, including collaboration with project leadership and local monitors to collaboratively achieve project milestones while also ensuring patient rights, wellbeing and safety are protected
Identifying potential research sites that align with the study's criteria and assessing their capabilities and resources.
Conduct initial site outreach, i.e., site engagement, collection of Confidentiality Agreement, and feasibility survey
Remote Pre-Study Visits and follow up documentation, including visit preparation, trip report completion, and other documentation as required to support site selection in line with sponsor, protocol, local and country regulations and requirements
Support customization and translation of informed consent forms and patient-facing materials.
Collect, track and perform a quality review of all essential documents required for effective and compliant study site activation from Site outreach, submissions, greenlight and until site activation. Maintenance and ongoing awareness of site regulatory compliance, supporting annual IRB/Independent Ethics Committee (IEC) renewals, PI change-over, and document expirations will be performed as applicable in compliance with local requirements.
Actively participate in study team meetings to support study progress, develop and implement action plans for site level risks, underperforming sites, or issues impacting project milestones and escalate issues in a timely manner
Support the CRA team in preparing for site initiation visits (SIVs) by coordinating with vendors, supplies teams, and study leads to ensure timely distribution of clinical study supplies, accesses and documents per study team guidance.
Responsible for submissions to and liaise with applicable IRB/IEC, Third Bodies (if applicable), and Regulatory Authorities by collaborating with Global Regulatory Submissions Lead (GRSL).
Perform initial contract and budget negotiations with the sites, as well as amended where applicable
Ensure high quality documents are filed in applicable systems in accordance with SOPs and project requirements and that the Trial Master File (TMF) is updated and audit ready at all times.
Track the progress of the start-up process and ensure that the research site meets all requirements and deadlines
Ensure Fortrea is audit ready by completing accurate, timely, and consistent system compliance on an ongoing basis
Serve as primary contact for investigative sites and ensure timely delivery in alignment with scope of work/study budget
Perform Case Review Form (CRF) review and data validation against source documentation according to protocol and guidelines as applicable in combination with monitoring for site protocol deviations, Serious Adverse Event (SAE) reporting, and all other duties as needed or assigned throughout the course of the study.
Perform country and site ICF review/customization, per local requirements
All other duties as needed or assigned

Qualifications (Minimum Required):

University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology) or 3-5 years' work experience in clinical research, including a strong working knowledge of the ICH/GCP guidelines and RA, IRB/IEC regulations.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
In lieu of the above requirement, candidates with a High School Diploma or equivalent AND a minimum of 5 years' work experience in clinical research, including a strong working knowledge of the ICH/GCP guidelines and RA, IRB/IEC regulations will be considered.
Fluent in local official language and in English, both written and verbal.

Experience (Minimum Required):

A scientific degree and/ or clinical expertise is optimal for this role.
Minimum of 3+ years of experience in clinical development or start-up/ regulatory process.
Thorough knowledge of ICH/GCP, RA, IRB/IEC, and other applicable regulations/guidelines; familiarity with investigator start-up documents and contract/budgets negotiation process; previous interaction with operational project teams and investigative sites.
Demonstrated understanding of research protocol requirements and proven ability to communicate them/educate others about them.
Effective communication with various stakeholders, including site staff, CRO personnel, and regulatory authorities.
Ability to manage multiple tasks and deadlines simultaneously, ensuring that all requirements are met in a timely manner.
Understanding of relevant regulations and guidelines related to clinical trials and research.
Ability to identify and resolve potential issues that may arise during the start-up process.
Ability to negotiate contracts and budgets effectively with research sites.
Employees will leverage their existing experience and skills to assume additional responsibilities within the broader role. These will be aligned with operational requirements and internal training, without altering the fundamental nature or classification of the position.

Physical Demands / Work Environment:

Remote-based work required with possible office presence depending on location
Travel requirements: Limited for training only

Learn more about our EEO & Accommodations request here .

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patient safety empleos en ciudad de méxico

Senior Site Navigator

Production Supervisor II

Clinical Research Physician

Operation Room Nurse

Medical Director

Life Sciences R&D Consultant/Manager

Local Clinical Project Manager

Post Market Complaints Data Analyst

Principal Clinical Scientist

Production Operator V

Nurse

DD&T, Instructional Designer (Sr.), Digital Dexterity

EHSS Platform Engineer

Key Account Manager

Nurse

Senior Embryologist (Bilingual Chinese & Spanish)

IT Support Engineer

AI / ML Engineer

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