CTA (Sponsor dedicated) en DOCS Global

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Celebramos 25 años

CTA (Sponsor dedicated)

Fecha de la oferta: 12 Sep.
Empresa que publica esta oferta: DOCS Global
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DOCS specialises in delivering strategic resourcing solutions to the biopharmaceutical and medical device industries and has been a leader in the field for over seventeen years since its establishment in 1997.

Our Services:
Our full-spectrum resourcing solutions include Functional Service Provision (FSP), Contract Placement, Permanent Placement and Executive Search.

Our Clients:
DOCS’ clients include all of the world’s top 20 pharma companies and a range of mid-sized pharma and biotech organisations.

Our History:
Founded in 1997, DOCS grew to become the premier staffing provider to the clinical development industry. The company was acquired by ICON plc. in 2007 and was merged wi
Número de vacantes: 1
Provincia/s: Madrid


Descripción: For our Client Top Pharmaceutical Company, DOCS (part of ICON plc) seeks a candidate with at least one year of experience as CTA.

The Clinical Trial Assistant administers, maintains and co-ordinates the logistical aspects of clinical trials according to Good Clinical Practice and relevant SOP's and acts as a pivotal point of contact for the clinical trial team and any contract organization used.

The Clinical Trial Assistant supporting the Clinical Research Associate to ensure optimal management of all documents with logistical and administrative tasks related to trial start-up, execution and and closing of clinical trials. Performs and regulatory document and approval, including site specific Informed Consents. Ensures trial related activities are in compliance with GCO SOPs, policies and local regulatory requirements.

Great opportunity to join in a Multinational Pharmaceutical Company!!!!
Edad máxima para el puesto: 65 años.
Tipo de contrato: Indefinido
Ventajas sociales o económicas: - Competitive salary and offer Social benefits
- As DOCS wants to keep a good work-life balance, we offer flexible working hours and some flexibility to work from home.


Requisitos: - At least 1 year relevant clinical trial experience or similar.
- Fluent in English, as well as the local language
- Excellent written and oral communication skills.
- Strong knowledge with MS Office.
Key competencies:
- Good organizational skills, ability to manage multiple tasks and meticulous attention to detail.
- Ability to perform activities in a timely and accurate manner.
Nivel de estudios mínimo requerido: Ciclo Formativo de grado superior / FP 2
Idiomas requeridos: Inglés nivel Alto.
Experiencia profesional mínima requerida: 1 año
Disponibilidad para viajar requerida: Ninguna

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Esta oferta ha recibido 89 inscripciones.