20 publicaciones de empleo destacadas de clinical scientist, clinical science, cronos en loreto cdmx (¡Están contratando!)

Senior Site Navigator
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Bachillerato
- Licenciatura
Senior Clinical Data Manager
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Licenciatura
Start-up Specialist
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Bachillerato
- Licenciatura
- Capacitación
Senior Regulatory & Start Up Specialist, cFSP
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Microsoft Office
- Licenciatura
Nursing Activity Manager to work in INTERNATIONAL HUMANITARIAN MISSIONS
Médicos Sin Fronteras en México A.C [Proyectos internacionales] —Ciudad de México, CDMX
- Desde $2,300 por mes
- Tiempo completo
- Enfermería
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- Inglés
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Medical Digital District & Omnichannel Lead
Eli Lilly —Ciudad de México, CDMX
- Tiempo completo
- Licenciatura
- Presencial
Sr. Project Management Analyst
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Licenciatura
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Proposal Associate
Precision for Medicine —Ciudad de México, CDMX
- Home Office (Desde casa)
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
Postulación rápida
Principal Clinical Database Manager
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Informática
- Licenciatura
Sr. Project Associate-ideal opportunity for CTA or Project Specialist (Hybrid CDMX- Mexico)
Syneos - Clinical and Corporate - Prod —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Microsoft Office
- Licenciatura
Associate, Project Manager
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Informática
- Inglés
- Licenciatura
Senior Clinical Programmer (Python)
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Informática
- Maestría
- SQL
Project Manager - Operations
Signant Health —Ciudad de México, CDMX
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Manager, COA Service Offerings & Quality
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Investigación
Assoc. Site Activation Manager - Sponsor Dedicated
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Licenciatura
- Terminología médica
Digital Medical Sales Manager
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Excel
- Experiencia en ventas
4d
SENIOR SOLUTIONS ARCHITECT (LatAm)
TransPerfect —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- Microsoft Excel
- Administración de personal
- Experiencia en ventas
Postulación rápida
14h
Analista de Datos para PSP
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- CRM software
- Microsoft Excel
- Ingeniería
- Oportunidades de crecimiento
Sales Representative
Beckman Coulter Life Sciences —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Disponibilidad para viajar hasta un 50 %
- Experiencia en ventas
- Seguro dental
- Vacaciones adicionales o permisos con goce de sueldo
Engagement Mgr, Technology Consulting
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Experiencia en ventas
- Inglés

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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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Quiero recibir la alerta de empleo más reciente para clinical scientist, clinical science, cronos en loreto cdmx

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