Contract Management Specialist en ABBVIE

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Celebramos 25 años

Contract Management Specialist

Fecha de la oferta: 21 Nov.
Empresa que publica esta oferta: ABBVIE
AbbVie (NYSE:ABBV) es una empresa biofarmacéutica global, basada en la investigación, que nace en 2013 tras la separación de Abbott. AbbVie combina el enfoque y la pasión de una empresa biotecnológica con la experiencia y la estructura de un líder farmacéutico. La misión de la compañía es utilizar su experiencia, el compromiso de sus empleados y su enfoque innovador único para desarrollar tratamientos avanzados para algunas de las enfermedades más complejas y graves del mundo.
Nuestro propósito es mejorar la vida de las personas y colaborar en la creación de soluciones médicas sostenibles.
Número de vacantes: 1
Provincia/s: Madrid

Descripción

Descripción: The Contract Management Specialist is responsible for the timely and appropriate execution of Confidentiality Disclosure Agreements (CDAs), Clinical Study Agreements (CSAs), associated Budgets, and vendor agreements, the legal sections of the Informed Consents and issues on other legal, compliance, regulatory and policy matters (such as Insurance Policies, FMV, FCPA, etc.). In partnership with Legal they ensure that issues and points of negotiation are settled rapidly in support of our new model to minimize or eliminate negotiation and our aspirational target of first pass acceptance of these documents. The overall aim is to keep CDAs, Contracts and Budgets off the clinical study critical path for all AbbVie studies (both Site Management & Monitoring and CRO conducted studies). The responsibility is Global – all countries except US, Puerto Rico and Japan.
Tipo de contrato: Indefinido

Requisitos

Requisitos: Appropriate tertiary qualification, health related (Medical, Scientific, Nursing) preferred. Other qualifications such as Legal and/ or Economic qualification will be valuated.
Minimum three years clinical research experience including contract/budget negotiation. Proven negotiating skills, tact and diplomacy.
Understanding of medical and legal terminology and the application of business/financial concepts used in clinical research.
Extensive knowledge related to ICH/GCP guidelines and applicable local regulations.
Ability to learn multiple concepts related to legal, compliance and regulatory matters in clinical research
Good planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines.
Ability to manage multiple priorities/projects.
Good written and verbal communication skills. Written and verbal fluency in English and local language (if not English).
Strong sense of urgency and ability to make decisions.
Nivel de estudios mínimo requerido: Licenciado
Idiomas requeridos: Inglés nivel Perfecto.
Experiencia profesional mínima requerida: 3 años
Disponibilidad para viajar requerida: Ninguna

Comparte esta oferta:

Esta oferta ha recibido 92 inscripciones.