20 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
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Consultant, Technology Consulting
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- Tiempo completo
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- Tiempo completo
- Inglés
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Principal Clinical Database Manager
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Informática
- Licenciatura
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Syneos - Clinical and Corporate - Prod —Ciudad de México, CDMX
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- Inglés
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Associate Proposals Developer
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Word
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Senior Clinical Data Manager
Fortrea —Ciudad de México, CDMX
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Site Management Associate I
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Medical Digital District & Omnichannel Lead
Eli Lilly —Ciudad de México, CDMX
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Precision for Medicine —Ciudad de México, CDMX
- Home Office (Desde casa)
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Postulación rápida
Associate, Project Manager
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Informática
- Inglés
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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

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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

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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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