20 publicaciones de empleo destacadas de quality coordinator en ciudad de méxico (¡Están contratando!)

Project Support Coordinator
Thermo Fisher Scientific —Ampliación Nápoles, CDMX
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
2d
MEP COORDINATOR
MUCHO TALENTO —Colonia del Valle, CDMX
- $40,000 a $43,000 por mes
- Tiempo completo
- Trabajo híbrido
- Administración de personal
- Inglés
- Licenciatura
- Estacionamiento gratuito
- Seguro dental
Postulación rápida
2d
Medical Information Specialist - Mexico City
Pfizer —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Microsoft Office
- Habilidades de comunicación
2d
Regulatory Submissions Associate/Senior Associate (Biological products)
Parexel —Ciudad de México, CDMX
- Administración de personal
- Inglés
- Licenciatura
2d
Marketing Communications Coordinator, Burger King, LAC
Burger King —Cuauhtémoc, CDMX
- Microsoft Powerpoint
- Microsoft Excel
- Administración de personal
- Permiso de maternidad y paternidad
Postulación rápida
3d
Client Success Operations Manager
OpsArmy —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Liderazgo
Postulación rápida
3d
Médico/a internista para Misiones Humanitarias Internacionales
MEDICOS SIN FRONTERAS EN MEXICO A.C. —Ciudad de México, CDMX
- Desde $27,000 por mes
- Tiempo completo
- Microsoft Excel
- Administración de personal
- Hospital
- Seguro de vida
Postulación rápida
Médico Urgenciólogo/a para Misiones Humanitarias Internacionales
MEDICOS SIN FRONTERAS EN MEXICO A.C. —Colonia Condesa, CDMX
- Desde $27,000 por mes
- Tiempo completo
- Microsoft Excel
- Hospital
- Inglés
- Seguro de vida
Postulación rápida
QA Coordinator
NBCUniversal —Colonia Lomas de Chapultepec, CDMX
- Tiempo completo
- Trabajo híbrido
- Bilingüe
- Administración de personal
- Inglés
Internal Medicine Physician for International Humanitarian Missions
Médicos Sin Fronteras en México A.C [Proyectos internacionales] —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Excel
- Administración de personal
- Hospital
- Seguro de vida
Service Manager
Vertiv —Ciudad de México, CDMX
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
CBS Accounting & Reporting Analyst
Colgate-Palmolive —Ciudad de México, CDMX
- ERP systems
- Inglés
- Licenciatura
5d
(Senior) Data Team Lead
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Licenciatura
- Liderazgo
Digital Project Manager
TransPerfect —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Excel
- Inglés
- Licenciatura
Postulación rápida
Customer Service Coordinator
QIMA —Ciudad de México, CDMX
- $28,000 a $30,000 por mes
- Tiempo completo
- Microsoft Excel
- Experiencia en ventas
- Servicio al cliente
Postulación rápida
Pediatra para Misiones Humanitarias Internacionales
MEDICOS SIN FRONTERAS EN MEXICO A.C. —Colonia Condesa, CDMX
- Desde $27,000 por mes
- Tiempo completo
- Microsoft Excel
- Hospital
- Inglés
- Seguro de vida
Postulación rápida
Executive Assistant - Bilingual
Hotel Rehabs —Ciudad de México, CDMX
- Tiempo completo
- Bilingüe
- Microsoft Excel
- Microsoft Outlook
Postulación rápida
Médico o Médica General - Misiones Humanitarias Internacionales
MEDICOS SIN FRONTERAS EN MEXICO A.C. —Ciudad de México, CDMX
- Desde $20,000 por mes
- Tiempo completo
- Microsoft Excel
- Hospital
- Inglés
- Seguro de vida
Postulación rápida
Knowledge Management Sr Analyst
PepsiCo —Miguel Hidalgo, CDMX
- Administración de personal
- Inglés
- Presupuestos
Account Manager (CDMX)
TransPerfect —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Servicio al cliente
- Inglés
Postulación rápida

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Project Support Coordinator

Thermo Fisher Scientific -
Ampliación Nápoles, CDMX

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Información del empleo

Tiempo completo
Hace 2 días

Cualificaciones

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Oracle
Administración de personal
Inglés
Microsoft Office
Recolección de datos
Administración del tiempo

Descripción completa del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as aProject Support Coordinator – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you’ll have the opportunity to independently provide administrative and technical support to project teams, including planning, organizing, and coordinating responsibilities at a global level. As a Project Support Coordinator, you'll drive and coordinate the initial study setup, ongoing maintenance of various systems, complete data entry, and maintain database repositories. You will prepare reports, collect data for analysis and reviews, and support audit readiness by ensuring files are reviewed on schedule, as detailed in the organization's SOPs/Client specific guidance document. You will contribute to the risk management process by timely identification and escalation of issues. You will support functional group and cross-functional initiatives for process improvements and enhancements. You may act as a main point of contact with the Project Lead (PL) or Clinical Team Manager (CTM) and provide oversight and coordination support to junior PSCs whenever required.

What You’ll Do:

Coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system. Follows up for resolution of findings and escalates whenever necessary.
Ensures allocated tasks are performed on time, within budget and to a high quality standard. Escalates in cases of variances (overburn/underburn).
Supports the maintenance and oversight of study specific documentation and global support with specific systems, tools and trackers including, but not limited to: study team lists, tracking of project specific training requirements, system access management for organization/vendor/clients, and tracking of project level activity plans in appropriate system.
Provides system (i.e. CTMS, Oracle Activate & eTMF) support by managing the access requests, tracking study level documents, maintaining audit readiness, communicating the non-compliance to the study team and suggesting resolution.
Performs administrative tasks on assigned trials including, but not limited to: timely processing of documents sent to CRG's/Client eTMF as required, performing CRG's/Client eTMF reviews, coordinating and proposing issue resolution, performing mass mailings and communications as needed, providing documents and reports to internal team members.
Supports scheduling and organization of client and/or internal meetings with completion and distribution of related meeting minutes and follow up for closure of action items, if required.
Exports and reconciles study metrics reports, and if required analyzes and identifies issues (if involved in a Lead role).
Maintains and regularly checks for correctness of vendor trackers.
Drives and coordinates the compilation of Investigator Site File (ISF) template, pharmacy binder with instruction from the Clinical Team Manager.
Attends Kick off and Project Launch meetings and takes notes when required, supports initial study set-up.

Education and Experience Requirements:

High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification
Technical positions may require a certificate
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years).

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Ability to work in a team or independently as required
Strong organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Strong customer focus
Excellent time management skills. Demonstrated flexibility to reprioritize workload to meet changing project timelines
Demonstrated ability to attain and maintain a good working knowledge of applicable Country
Regulations (if required), ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout
Excellent English language and grammar skills and proficient local language skills (if required).
Effective oral and written communication skills with the ability to communicate effectively with project team members
Excellent computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain
knowledge and learn the required clinical trial systems. Good presentation skills.
Ability to successfully complete CRG training program
Self-motivated, positive attitude and good interpersonal skills

Working Conditions and Environment:

Work is performed in an office or clinical environment with exposure to electrical office equipment.
Occasional drives to site locations. Potential Occasional travel required.

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MEP COORDINATOR

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Quiero recibir la alerta de empleo más reciente para quality coordinator en ciudad de méxico

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