20 publicaciones de empleo destacadas en ppd (¡Están contratando!)

Trial Delivery Specialist - Clinical Trial Coordinator
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
4d
Clinical Research Associate II
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Enfermería
- Administración de personal
- Inglés
Country Approval Associate
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Inglés
- Licenciatura
- Uso de computadora
5d
Sr Dir Ops - Medical Communications
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Administración de personal
- Doctorado
- Liderazgo
Clinical Trial Coordinator II
Thermo Fisher Scientific —Ampliación Nápoles, CDMX
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
4d
Global Clinical Supplies Project Manager
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Servicio al cliente
- Inglés
- Microsoft Office
5d
PPD / Production Print Field Engineer - Central Belt
Pure Talent Group —City, Hgo.
- Turno de 12 horas
9d
Safety Committee Specialist - Adjudication
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Project Budget Coordinator
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Administración de personal
- Servicio al cliente
- ERP systems
AUXILIAR CONTABLE DE CUENTAS POR PAGAR
FERREBAZTAN SA DE CV —Segunda Fracción de Crespo (Alto del Parral), Gto.
- $13,000 por mes
- Tiempo completo
- Microsoft Excel
- ERP systems
- Licenciatura
- Descuentos y precios preferenciales
- Seguro de vida
Postulación rápida
Técnico PPD / Técnica PPD
ENGIE —Lázaro Cárdenas (Zona Hornos), Méx.
- Tiempo completo
- Ingeniería
- Mantenimiento
- Microsoft Office
13d
PPD Print Production Field Service Engineer - North West
Pure Talent Group —City, Hgo.
10d
Analista de Cuentas por Cobrar
KUKA SYSTEMS DE MEXICO —Parque industrial Toluca 2000, Méx.
- $21,000 a $23,000 por mes
- Tiempo completo
- Trabajo híbrido
- Inglés
- Seguro de gastos médicos
- Vacaciones adicionales o permisos con goce de sueldo
Postulación rápida
Analista de Nominas
NRD SOLUCIONES —Atizapán de Zaragoza, Méx.
- $15,000 a $16,500 por mes
- Tiempo completo
- Microsoft Excel
- ERP systems
- Microsoft Office
- Oportunidades de crecimiento
Postulación rápida
5d
ASISTENTE ADMINISTRATIVO FACTURACION
ACHEME —Coyoacán, CDMX
- $12,000 por mes
- Aplicaciones en linea
- Finanzas
- Licenciatura
- Contaduría
Postulación rápida
Analista Contable
GRUPO GUIA —Lomas de Providencia, Jal.
- $18,000.00 a $21,493.97 por mes
- Tiempo completo
- Licenciatura
- Sin título de educación superior
- Contabilidad general
Postulación rápida
11d
Contador Público
MENSCH MEXICO —Naucalpan, Méx.
- $22,000 a $23,000 por mes
- Tiempo completo
- Licenciatura
- Contabilidad general
- Habilidades de organización
- Seguro de vida
Postulación rápida
Analista Contable
MENSCH MEXICO —Cuauhtémoc, CDMX
- $14,000 a $16,000 por mes
- Incluye fines de semana
- Microsoft Excel
- Licenciatura
- Contabilidad general
Postulación rápida
9d
Auxiliar de Facturación y Cobranza
PETRO —Salamanca Centro, Gto.
- $7,118.98 a $13,620.83 por mes
- Correo electrónico
- Contabilidad general
- Contaduría
- Estacionamiento gratuito
Postulación rápida
Junior Accounting Analyst
FOREO —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Excel
- Inglés
- Licenciatura
Postulación rápida

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Trial Delivery Specialist - Clinical Trial Coordinator

Thermo Fisher Scientific -
Desde casa

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Información del empleo

Tiempo completo
Hace 4 días

Cualificaciones

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Inglés
Microsoft Office
Experiencia en bases de datos
Licenciatura
Uso de computadora

Descripción completa del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Clinical Trial 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 provide administrative and technical support to the Project Team. As a Senior Clinical Trial Coordinator, you'll coordinate and facilitate project activities and may serve as a study lead, acting as a cross-functional liaison for the project team. You will act as a buddy during the onboarding phase and provide training to new staff as needed. Additionally, you will support departmental and cross-functional initiatives for process improvements and enhancements.

What You’ll Do:

According to the specific role (Central or Local), 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.
Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate.
Supports the maintenance 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. Ensures (e)TMF is up to date by following file review schedules and documents findings in appropriate system.
Provides system support (i.e. GoBalto & eTMF).
Supports RBM activities.
Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, 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 of related meeting minutes.
Reviews and tracks local regulatory documents.
Transmits documents to client and centralized IRB/IEC.
Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.
Maintains vendor trackers.
Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites.
Assists with study-specific translation materials and translation QC upon request.
May attend Kick off meeting and take notes when required.

Education and Experience Requirements:

High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
Bachelor's degree preferred.
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 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
Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines
Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, 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 as needed
Good presentation skills
Excellent computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
Ability to successfully complete PPD clinical training program
Self-motivated, positive attitude with effective strong interpersonal skills

Working Conditions and Environment:

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

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