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

Safety Associate
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Microsoft Office
1d
Site Contract Specialist I
PSI CRO —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Postulación rápida
1d
Connected Devices Project Manager
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Servicio al cliente
- Microsoft Office
1d
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
3d
VALUADOR DE SINIESTROS hyp
SARSAN AUTOMOTRIZ —Portales Norte, CDMX
- $10,800 a $14,800 por mes
- Aplicaciones en linea
- Administración de personal
- Bachillerato
- Licenciatura
Postulación rápida
Enfermera Educadora para PSP Zona Tijuana.
IQVIA —Ciudad de México, CDMX
- Aplicaciones en linea
- Enfermería
- Licenciatura
- Habilidades de comunicación
Senior Data Engineer
SimplePractice —Ciudad de México, CDMX
- Administración de personal
- Informática
- DevOps
- Seguro dental
- Seguro de la vista
Postulación rápida
Senior Software Engineer II - Java Fullstack
Elsevier —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Informática
- Java
- Seguro dental
- Permiso de maternidad y paternidad
Senior Software Engineer II - Java Fullstack
RELX —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Informática
- Java
- Seguro dental
- Permiso de maternidad y paternidad
Senior Clinical Data Engineer (LATAM)
Precision for Medicine —Ciudad de México, CDMX
- Home Office (Desde casa)
- Administración de personal
- Inglés
- SQL
Postulación rápida
Senior Clinical Data Engineer (LATAM)
Precision Medicine Group —Ciudad de México, CDMX
- Home Office (Desde casa)
- Administración de personal
- Inglés
- SQL
Clinical Community Analyst
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Enfermería
- Administración de personal
- Análisis de datos
1d
Operations Specialist 1
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Experiencia en bases de datos
- Licenciatura
1d
Studio Project Manager
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- PMP
- Inglés
1d
Gerente de Nacional Ventas | Línea Respiratoria
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Experiencia en ventas
- Inglés
- Maestría
- Oportunidades de crecimiento
7h
Gerente de Ventas | Línea Respiratoria
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Experiencia en ventas
- Mercadotecnia
- Inglés
- Oportunidades de crecimiento
7h
Software Engineer II
Helix —Ciudad de México, CDMX
- $63,083 a $81,563 por mes
- Tiempo completo
- Home Office (Desde casa)
- Administración de personal
- Inglés
- Java
- Vacaciones adicionales o permisos con goce de sueldo
8h
Senior Software Engineer
Helix —Ciudad de México, CDMX
- $101,333 a $150,750 por mes
- Tiempo completo
- Home Office (Desde casa)
- Azure
- Informática
- Inglés
- Vacaciones adicionales o permisos con goce de sueldo
8h

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Safety Associate
IQVIA —Ciudad de México, CDMX
Bachelor’s degree in Life sciences or a related field (mandatory). 1 or 2 years of pharmacovigilance experience will be highly valued (desirable).
1d
Site Contract Specialist I
PSI CRO —Ciudad de México, CDMX
College/University degree or an equivalent combination of education, training & experience. Knowledge and experience with legal documents related to clinical…
Postulación rápida
1d

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Safety Associate

IQVIA -
Ciudad de México, CDMX

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Información del empleo

Tiempo completo
Hace 1 día

Cualificaciones

Administración de personal
Plurilingüe
Inglés
Microsoft Office
Experiencia en bases de datos
Licenciatura
Administración del tiempo

Descripción completa del empleo

Mexico City, Mexico | Full time | Home-based | R1567378

Job Overview

Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.

Essential Functions

To Prioritize and complete the assigned trainings on time.
Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.
To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information
Database entry
Coding AE and Products, writing narratives, Literature related activities as per internal/project timelines.
Ensure to meet quality standards per project requirements.
Ensure to meet productivity and delivery standards per project requirements.
Creating, maintaining and tracking cases as applicable to the project plan.
Identify quality problems, if any, and bring them to the attention of a senior team member.
To mentor new teams members, if assigned by the Manager.
Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.
100% compliance towards all people practices and processes
Perform other duties as assigned.

Qualifications

Bachelor’s degree in Life sciences or a related field (mandatory)
Fluency in English and Spanish (mandatory) (will be evaluated)
1 or 2 years of pharmacovigilance experience will be highly valued (desirable)
Experience with Safety Databases will be highly valued (ARGUS or others) (desirable)
Knowledge of applicable global, regional, local clinical research regulatory requirements. (desirable)
Excellent attention to detail and accuracy.
Good working knowledge of Microsoft Office and web-based applications.
Strong organizational and time management skills, with the ability to multitask and manage competing priorities and deadlines.
Strong verbal/written communication skills. Intermediate
Self-motivated and flexible. Intermediate

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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clinical scientist, clinical science, cronos empleos en loreto cdmx

Safety Associate

Site Contract Specialist I

Connected Devices Project Manager

SENIOR SOLUTIONS ARCHITECT (LatAm)

VALUADOR DE SINIESTROS hyp

Enfermera Educadora para PSP Zona Tijuana.

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Senior Software Engineer II - Java Fullstack

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Operations Specialist 1

Studio Project Manager

Gerente de Nacional Ventas | Línea Respiratoria

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