20 publicaciones de empleo destacadas de study start up lead en spain (¡Están contratando!)

Assistant CRA
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Servicio al cliente
- Inglés
- Microsoft Office
8d
CTM/Sr CTM - FSP - EMEA
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Microsoft Word
- Microsoft Excel
- Inglés
1d
Global Study Associate Director
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Doctorado
- Investigación
12d
Director, Alliance Management (Alliance Lead)
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Investigación
- Project management
12d
Senior CTM, Non-Interventional/Observational Studies
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Microsoft Word
- Microsoft Excel
- Inglés
3d
Client Success Partner - Enterprise
360Learning —En remoto
- Jornada completa
- Teletrabajo
- Inglés
- Máster
- Habilidades de comunicación
- Teletrabajo opcional
Project Manager: Design
The Design Agency —Barcelona, Barcelona provincia
- Jornada completa
- AutoCAD
- Inglés
- Oficina
Solicitud rápida
Director, Study Management
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Grado
- Gestión de conflictos
8d
Business Development Representative DACH
360Learning —En remoto
- Jornada completa
- Teletrabajo
- Ventas
- Salesforce
- Inglés
- Teletrabajo opcional
Student Success Advisor - Seville
Verto Education —Sevilla, Sevilla provincia
- De guardia
- Inglés
- Grado
Solicitud rápida
5d
Senior Clinical Trial Manager - Internal Medicine
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
- Liderazgo
- Seguro dental
- Seguro oftalmológico
Content Marketer, Enterprise Sales
AirDNA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- CRM software
- Español
- Ventas
- Seguro dental
- Teletrabajo opcional
Global Development Director Scientist
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Doctorado
- Investigación
5d
PhD researcher
BCBL Basque Center on Cognition, Brain & Language —Donostia-San Sebastián, Guipúzcoa provincia
- Media jornada
- Español
- Doctorado
- Inglés
Global Development Senior Medical Director, Hematology Oncology
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Investigación
- Oficina
9d
Clinical Trial Coordinator
Thermo Fisher Scientific —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
12d
Global Digital Product & Experience Manager
HSE Santander Insurance S.L —Boadilla del Monte, Madrid provincia
- Jornada completa
- Español
- Marketing
- Inglés
- Abono gimnasio
- Seguro de vida
Lead Infrastructure Operations Engineer
Schneider Electric —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Azure
- Informática
- Sistemas ERP
- Días de asuntos propios
- Teletrabajo opcional
8d
Senior Product Manager - Education vertical (eduQa)
SeQura —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- Grado
Solicitud rápida
Senior Business Development Director (m/f/d)
Optimapharm d.o.o. —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Investigación
- Máster

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Assistant CRA

Thermo Fisher Scientific -
En remoto

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Detalles del empleo

Jornada completa
Hace 8 días

Cualificaciones

Servicio al cliente
Inglés
Microsoft Office
Grado
Habilidades de comunicación
Gestión del tiempo

Descripción completa del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Spain: Madrid and Barcelona ONLY

Join Us as an Assistant Clinical Research Associate – 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 perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead. As an Assistant Clinical Research Associate, you'll provide support with site preparedness, logistical support to the monitoring process, and assist with assigned tasks for site management and remote monitoring in accordance with SOPs and regulatory guidelines. You may be assigned limited site contact activities during study start-up, site management, recruitment, and close-out phases.

What You’ll Do:

Completes study and site management activities as defined in task matrix, andas applicable and directed for study assigned.
Completes and documents study-specific training.
Orients and trains on any study-specific systems.
Provides in-house support during pre-study assessments and with pre-study assessment waivers, as agreed for project.
Supports to customize Site ICF with site contact details, as needed.
Performs remote review of EMR/EHR checklist and supports collection, as applicable assessments.
Verifies document collection and RCR submission status; updates site EDL and verifies site information.
Reviews patient facing materials and review translations, as directed.
Supports site staff with the vendor related qualification process, where applicable.
Provides support by ensuring system access is requested/granted and revoked for relevant site staff during pre-activation and subsequent course of the study.
Provides support to follow-up on site staff training, as applicable.
Coordinates and supports logistics for IM attendance, as directed.
Supports maintenance of vendor trackers, as directed.
Coordinates study/site supply management during pre-activation and subsequent course of the study.
Supports Essential Document collection, review and updating in systems, as applicable.
Follows up and supports on missing study vendor data like ECGs, lab samples, and e-diaries, as directed.
Supports ongoing remote review of centralized monitoring tools, as directed.
Supports Site payments processes by coordinating with various functional departments within organization and site. Supports system updates and reconciliations, as directed and follows-up on site invoices throughout the study period.
Performs reconciliation tasks on assigned trials including but not limited to CRF and query status, deviations, SAEs and safety reports, as applicable.
Verifies document collection status in company systems and drives action for missing/incomplete/expired documents and open document findings, as directed.
May perform other assigned site management tasks, as directed by CRA and as per Task Matrix.
May perform a specific role profile for FSP opportunities according to Client requests.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.

Education and Experience Requirements:

Bachelor's degree in a life science discipline or related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 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:

Basic medical/therapeutic area knowledge and understanding of medical terminology
Ability to attain and maintain a working knowledge of ICH GCP, applicable regulations and company procedural documents
Effective oral and written communication skills
Excellent interpersonal and customer service skills
Good organizational and time management skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Proven flexibility and adaptability
Ability to work in a team or independently, as required
Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Proficient computer skills with good knowledge of MS Office ability to learn and use appropriate software. Leverage modern technology when applicable
Ability to extract pertinent information from all study documents, electronic study data systems, CTMS and dashboards
Excellent English language and grammar skills

Working Conditions and Environment:

Work is performed most of the time in an office or home office environment.; occasional travel toclinics/hospitals may be required.
Exposure to electrical office equipment.
The Assistant CRA role does not involve regular travel, however, any direct, promotional opportunities in the CRA career track will require frequent travel (60-80%).

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study start up lead empleos en spain

Assistant CRA

CTM/Sr CTM - FSP - EMEA

Global Study Associate Director

Director, Alliance Management (Alliance Lead)

Senior CTM, Non-Interventional/Observational Studies

Client Success Partner - Enterprise

Project Manager: Design

Director, Study Management

Business Development Representative DACH

Student Success Advisor - Seville

Senior Clinical Trial Manager - Internal Medicine

Content Marketer, Enterprise Sales

Global Development Director Scientist

PhD researcher

Global Development Senior Medical Director, Hematology Oncology

Clinical Trial Coordinator

Global Digital Product & Experience Manager

Lead Infrastructure Operations Engineer

Senior Product Manager - Education vertical (eduQa)

Senior Business Development Director (m/f/d)

Quiero recibir la alerta de empleo más reciente de study start up lead en spain

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