Empleos actuales relacionados con Reg Affairs Spec - Desde casa - Thermo Fisher Scientific

  • Sr Reg Affairs Spec

    hace 2 semanas

    Desde casa, México Thermo Fisher Scientific A tiempo completo

    At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

  • Reg Affairs Assistant

    hace 3 semanas

    Desde casa, México Thermo Fisher Scientific A tiempo completo

    **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Essential Functions and Other Job Information**: - Provides administrative support to the department. - Assist with projects’ archiving of documents and submissions. - Provides project specific services, documentation and coordination of projects and supports reporting of same...

  • Clinical Trial Reg Affairs Specialist Ii

    hace 3 semanas

    Desde casa, México Thermo Fisher Scientific A tiempo completo

    Act as an administrator for our in-house Regulatory Intelligence database and provide customer support for issues arising. - Regulatory collaboration with Regulatory Intelligence database workflow users to drive quarterly EQR metrics. - Contribute to a wide range of technical Regulatory Intelligence database content projects including engineering and...

Reg Affairs Spec

hace 4 semanas

Desde casa, México Thermo Fisher Scientific A tiempo completo

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office
- Prepares and reviews regulatory submissions.
- Provides regulatory strategy and/or technical advice to internal and external clients, and acts as a liaison in executing strategies.
- Leads the development and implementation of project-specific processes for sponsors.
- Collaborates with other departments, regulatory consultants, and regulatory authorities.
- Assists in identifying and recognizing out of scope activities in a contract in a timely manner and liaises with other departments to follow through on all aspects of contract modifications.
- Participates in project launch meetings, review meetings and project team meetings.
- Supports business development activities, including project budgeting/forecasting.
- Requires
- Not mandatory but preferred experience clinical trials submissions and development
- Good organizational and planning skills to effectively manage shifting priorities
- Capable of working effectively on a team and/or independently with mínimal supervision
- Good electronic document production skills
- Good attention to detail and quality of documentation
- Good interpersonal skills with the ability to interact with customers
- Solid verbal and written communication skills
- Capable of multitasking and managing multiple projects