Senior Regulatory Submissions Associate
hace 6 días
source : DirectEmployers Association

Job Overview : Covance is expanding and is looking to recruit a Senior Regulatory Submissions Associate to join the team, candidates can be based anywhere in the EMEA region.

The role is responsible for the timely preparation of submissions to Regulatory Authorities in support of investigational and marketed products.

You will Interact with Regulatory Authorities and with clients to support regulatory activities. Proactively interact with other Covance groups and clients to provide guidance regarding Regulatory Authority requirements and project timelines and requirements.

Working with minimal supervision, it is the responsibility of the Senior Regulatory Associate to prepare documents to the required standard and to maintain awareness of current regulatory standards related to submissions for drug and biologic products.

Education / Qualifications : Bachelor's Degree in Life Sciences or equivalent Experience : Candidates should have experience performing submissions to Regulatory Authorities.

Have excellent communication skills, organization and planning skills and have high attention to detail. Be able to communicate effectively in the English language.

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority / Female / Individual with Disability / Veteran / Sexual Orientation / Gender Identity).

Your confidentiality and privacy are important to us.

Añadir a favoritos
Eliminar de mis favoritos
Mi Correo Electrónico
Al hacer clic en la opción "Continuar", doy mi consentimiento para que neuvoo procese mis datos de conformidad con lo establecido en su Política de privacidad . Puedo darme de baja o retirar mi autorización en cualquier momento.
Formulario de postulación