Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
RA Consultant - Belgium - Excellent Rates
Eingestellt von Vivid Resourcing Ltd
Gesuchte Skills: Consultant, Client
Projektbeschreibung
A global Pharmaceutical client I am working with is currently looking for a Regulatory Affairs Submission Manager to join them on a contract basis for 12 months.
MAIN RESPONSIBILITIES:
- Establishing Dossier Plans for the assigned submission types/projects considering inputs from functional area representatives and key stakeholders
- Meeting regularly with submission stakeholders to identify and resolve issues and to assess quality and delivery of Dossier Plans
- Monitoring the effectiveness of appropriate submission processes with responsibility for initiating changes within the scope of decision-making authority to minimize inefficiencies and ensure quality
- Meeting regularly with submission stakeholders to identify and resolve issues and to assess quality and delivery of Dossier Plans, quality of deliverables and timelines against established KPIs
- Manage preparation and/or publishing of submissions across the product lifespan in line with Regulatory strategy
- Ensure that all required documents are included in the dossier
- Track submission events/activities in appropriate systems/tools
KEY REQUIREMENTS:
- University or Bachelor degree
- 2-4 years of experience required in the pharmaceutical industry or related experience
- Works well across functions and groups; builds teams effectively; inspires follower ship; instils a global mind set; champions best practices
- Able to persuade, convince, or influence others, in order to gain support for an idea or a course of action he/she wants others to adopt
VACANCY SUMMARY:
Job type: Contract
Duration: 12 months
Location: Belgium
Rate: Negotiable
If you are interested in this role or know anyone who might be please get in touch with an up to date CV and I'll be in touch.
MAIN RESPONSIBILITIES:
- Establishing Dossier Plans for the assigned submission types/projects considering inputs from functional area representatives and key stakeholders
- Meeting regularly with submission stakeholders to identify and resolve issues and to assess quality and delivery of Dossier Plans
- Monitoring the effectiveness of appropriate submission processes with responsibility for initiating changes within the scope of decision-making authority to minimize inefficiencies and ensure quality
- Meeting regularly with submission stakeholders to identify and resolve issues and to assess quality and delivery of Dossier Plans, quality of deliverables and timelines against established KPIs
- Manage preparation and/or publishing of submissions across the product lifespan in line with Regulatory strategy
- Ensure that all required documents are included in the dossier
- Track submission events/activities in appropriate systems/tools
KEY REQUIREMENTS:
- University or Bachelor degree
- 2-4 years of experience required in the pharmaceutical industry or related experience
- Works well across functions and groups; builds teams effectively; inspires follower ship; instils a global mind set; champions best practices
- Able to persuade, convince, or influence others, in order to gain support for an idea or a course of action he/she wants others to adopt
VACANCY SUMMARY:
Job type: Contract
Duration: 12 months
Location: Belgium
Rate: Negotiable
If you are interested in this role or know anyone who might be please get in touch with an up to date CV and I'll be in touch.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung, Organisation/Management