20 publicaciones de empleo destacadas de clinical research en en remoto (¡Están contratando!)

Assistant CRA
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Servicio al cliente
- Inglés
- Microsoft Office
Medical Writer (FSP) - Client Aligned
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Grado
- Control de calidad
7d
Senior Medical Writer (Regulatory) - Multi-Sponsor
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Microsoft Excel
- Investigación
- Project management
Regional Clinical Study Manager
BeiGene —En remoto
- De 71.400 € a 89.200 € al año
- Jornada completa
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
10d
FSP Principal Medical Writer (Regulatory) - Client-Dedicated
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Project management
- Habilidades de presentación
- Grado
Clinical Operation Manager FSP, Barcelona
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Gestión de conflictos
Senior Contract Associate, Clinical Site Contracts
BeiGene —En remoto
- De 57.600 € a 72.000 € al año
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Microsoft Office
Senior Medical Writer – Client Aligned (FSP)
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Grado
- Control de calidad
- Liderazgo
Clinical Scientist Director - Late Development Oncology
Amgen —En remoto
- De 131.166,90 € a 177.461,10 € al año
- Teletrabajo
- Doctorado
- Máster
- Grado
- Seguro dental
- Seguro oftalmológico
Senior Medical Writer - Early Phase (Single Sponsor Support)
サイネオス・ヘルス —En remoto
- Teletrabajo
- Inglés
- Investigación
Senior Medical Project Coordinator, EMEA
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Enfermería
- Investigación
- Project management
FSP Site Budget & Contracting Lead
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Habilidades de comunicación
PV Manager Safety Science
Thermo Fisher Scientific —En remoto
- Horas extra
- Teletrabajo
- Inglés
- Microsoft Office
- Project management
CRA I. Valencia. Sponsor dedicated.
サイネオス・ヘルス —En remoto
- Teletrabajo
- Grado
(Associate) Medical Director - Neurology
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Inglés
- Experiencia hospitalaria
11d
Senior Director of Qualitative Data Collection and Analysis
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Doctorado
- Inglés
- Investigación
MSL - Based in Madrid
Mundipharma —En remoto
- Jornada completa
- Teletrabajo
- Microsoft Powerpoint
- Español
- Doctorado
Principal Statistician - Ophthalmology - Fully remote in Europe
サイネオス・ヘルス —En remoto
- Teletrabajo
- Doctorado
- Inglés
- Máster
7d
Principal Statistician - Early Phase - Fully home based (remote anywhere in Europe) Sponsor Dedicated
サイネオス・ヘルス —En remoto
- Teletrabajo
- Doctorado
- Inglés
- Máster
9d
Radiologist Full-time
Telemedicine Clinic —En remoto
- Jornada completa
- Teletrabajo
- Inglés
- Teletrabajo opcional

Quiero recibir la alerta de empleo más reciente de clinical research en en remoto

Al iniciar sesión en tu cuenta, aceptas las Condiciones del servicio de SimplyHired, nuestra Política sobre cookies y nuestra Política de privacidad.

Explorar empleos en más ubicaciones

clinical research jobs near en remoto

Empleos de Clinical Research Associate en En Remoto

Empleos de Medical Writer en En Remoto

Empleos de Economics Research en Madrid, Madrid Provincia

Empleos de Clinical Research Associate en Madrid, Madrid Provincia

Empleos de Clinical Research Associate en Barcelona Provincia

Empleos de Associate en Santander, Cantabria Provincia

Empleos de Cta, Clinical Trials Assistant en Madrid, Madrid Provincia

Empleos de Site Lead en Rota, Cádiz Provincia

Empleos de Talent Acquisition Lead en Barcelona, Barcelona Provincia

Empleos de Qa Lead en Barcelona Provincia

Empleos de Qa Lead en Madrid, Madrid Provincia

Empleos de Site Lead en Barcelona, Barcelona Provincia

Empleos de Team Lead en Barcelona, Barcelona Provincia

Empleos de Site Lead en Viana, Navarra Provincia

Empleos de Medical Affairs en Alcalá De Henares, Madrid Provincia

Empleos de Medical Writer en Madrid Provincia

Empleos de Events Coordinator en Costa Maresme, Barcelona Provincia

Empleos de Events Coordinator en Zona Universitaria, Barcelona Provincia

Empleos de Junior Project Manager en Madrid, Madrid Provincia

Empleos de Director Marketing en En Remoto

Assistant CRA

Thermo Fisher Scientific -
En remoto

Solicitar ahora

Detalles del empleo

Jornada completa

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%).

Solicitar ahora

Refina tu búsqueda

clinical research empleos en en remoto

Assistant CRA

Medical Writer (FSP) - Client Aligned

Senior Medical Writer (Regulatory) - Multi-Sponsor

Regional Clinical Study Manager

FSP Principal Medical Writer (Regulatory) - Client-Dedicated

Clinical Operation Manager FSP, Barcelona

Senior Contract Associate, Clinical Site Contracts

Senior Medical Writer – Client Aligned (FSP)

Clinical Scientist Director - Late Development Oncology

Senior Medical Writer - Early Phase (Single Sponsor Support)

Senior Medical Project Coordinator, EMEA

FSP Site Budget & Contracting Lead

PV Manager Safety Science

CRA I. Valencia. Sponsor dedicated.

(Associate) Medical Director - Neurology

Senior Director of Qualitative Data Collection and Analysis

MSL - Based in Madrid

Principal Statistician - Ophthalmology - Fully remote in Europe

Principal Statistician - Early Phase - Fully home based (remote anywhere in Europe) Sponsor Dedicated

Radiologist Full-time

Quiero recibir la alerta de empleo más reciente de clinical research en en remoto

Related Searches

Explorar empleos en más ubicaciones

Herramientas para candidatos

Herramientas para empresas

Buscar

Mantener la conexión