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

Centralized Monitoring Lead in LATAM (Remote)
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- Inglés
- Licenciatura
Safety Specialist II - Mexico and Argentina - Hybrid
サイネオス・ヘルス —Tlalnepantla, Méx.
- Contratos
8h
Site Management Associate
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Licenciatura
- Disponible para viajar
- Seguro dental
- Seguro de la vista
9h
Project Associate-ideal opportunity for CTA or Project Specialist (Hybrid, Ciudad de Mexico)
Syneos - Clinical and Corporate - Prod —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Microsoft Office
- Licenciatura
Associate Decentralized Clinical Trial Lead / Decentralized Clinical Trial Lead
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Licenciatura
Principal Statistical Programmer (Clinical Trials)
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Informática
- Inglés
Analyst (Consulting)
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Maestría
- Licenciatura
Nursing Activity Manager to work in INTERNATIONAL HUMANITARIAN MISSIONS
MEDICOS SIN FRONTERAS EN MEXICO A.C. —Ciudad de México, CDMX
- Desde $39,333 por mes
- Tiempo completo
- Enfermería
- Microsoft Excel
- Inglés
- Seguro de vida
Postulación rápida
Data Manager for Clinical Trials
PSI CRO —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- Oracle
- Administración de personal
- Inglés
Postulación rápida
Safety Specialist II - Mexico and Argentina - Hybrid
Syneos - Clinical and Corporate - Prod —Ciudad de México, CDMX
- Tiempo completo
- Contratos
9h
Site Specialist II
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Licenciatura
- Sin título de educación superior
- Habilidades de organización
- Seguro dental
- Seguro de la vista
9h
Central Monitor in LATAM
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Enfermería
- Microsoft Excel
- Inglés
Clinical Start-Up & Trial Lead (Start-Up + CTL)
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Licenciatura
- Disponible para viajar
Drug Safety Physician
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Licenciatura
- Seguro dental
- Seguro de la vista
Safety & PV Specialist II - Mexico Hybrid
サイネオス・ヘルス —Tlalnepantla, Méx.
- Contratos
Life Sciences R&D Consultant/Manager
Accenture —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Maestría
Consulting Intern
IQVIA —Ciudad de México, CDMX
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Lead Clinical Research Associate
PSI CRO —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- Inglés
- Microsoft Office
- Licenciatura
Postulación rápida
Clinical Scientist in CNS - LATAM
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Maestría
Logistics Manager for México, Costa Rica & El Salvador
Siemens Healthineers —Ciudad de México, CDMX
- Tiempo completo
- Trabajo híbrido
- Licenciatura
- Negocios
- Liderazgo
2d

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Centralized Monitoring Lead in LATAM (Remote)

IQVIA -
Ciudad de México, CDMX

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Información del empleo

Tiempo completo

Cualificaciones

Inglés
Licenciatura

Descripción completa del empleo

Mexico City, Mexico | Full time | Home-based | R1558548

Job Overview

The Leader of the Centralized Monitoring team, partner with the project and clinical lead to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction per contract, while optimizing speed, quality and cost of delivery and in accordance with IQVIA SOPs, policies and practices.

Essential Functions:

Leadership activities:
- Leader of the Centralized Monitoring team, partner with the project and clinical lead to perform oversight on clinical deliverables on global assigned projects as per the protocol, SOPs, respective regulation/guidelines and project Clinical Operations Plan.
- Unblinded Clinical Lead, including IP management for the assigned study to identify risk and proposed mitigation (including re-supply, re-labelling, Import/export licenses etc.)
- May act as Clinical Lead when there is not assigned to the study and at project close out.
- Manage project resources (CRAs/ Central Monitors/ Clinical Trial Assistants/ Centralized Monitoring Assistants)
Analytical activities:
- Manage, monitor and complete study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan, review, triage and action clinical study alerts, monitor clinical operation plan compliance etc.).
- Contribute to developing the study specific analytics strategy and work on developing advanced analytics.
Support project management team to develop monitoring strategy, including monitoring triggers/thresholds.
Attend study team and /or client meetings.
Provide Inputs to clinical study teams, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections.
Development and use of study management plans, and/or RBM specific tools and templates, and/or other study specific plans to evaluate the quality and integrity of the study.
Ensure complete and accurate documentation of all the study specific tools and templates and keep the project Audit ready, including eTMF oversight.
Mentors or coaches for junior staff.

Qualifications:

Bachelor's degree in life sciences or related field.
+3 years of relevant clinical monitoring experience (as remote or on site CRA). Advanced knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
+2 years in a Lead role.
Strong written and verbal communication skills including advanced command of English (Mandatory).
Strong organizational, problem solving and decision making skills.
Results and detail-oriented approach to work delivery and output.
Excellent motivational, influencing, negotiating and coaching skills.
Ability to work on multiple global projects and manage competing priorities.
To lead team and effectively work in team.

#LI-NRJ #LI-Remote

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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Refina tu búsqueda

clinical scientist, clinical science, cronos empleos en loreto cdmx

Centralized Monitoring Lead in LATAM (Remote)

Safety Specialist II - Mexico and Argentina - Hybrid

Site Management Associate

Project Associate-ideal opportunity for CTA or Project Specialist (Hybrid, Ciudad de Mexico)

Associate Decentralized Clinical Trial Lead / Decentralized Clinical Trial Lead

Principal Statistical Programmer (Clinical Trials)

Analyst (Consulting)

Nursing Activity Manager to work in INTERNATIONAL HUMANITARIAN MISSIONS

Data Manager for Clinical Trials

Safety Specialist II - Mexico and Argentina - Hybrid

Site Specialist II

Central Monitor in LATAM

Clinical Start-Up & Trial Lead (Start-Up + CTL)

Drug Safety Physician

Safety & PV Specialist II - Mexico Hybrid

Life Sciences R&D Consultant/Manager

Consulting Intern

Lead Clinical Research Associate

Clinical Scientist in CNS - LATAM

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