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Regulatory Manager
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Client, Marketing
Projektbeschreibung
Regulatory Manager wanted for our Basel based client in the pharmaceutical industry.
YOUR EXPERIENCE/SKILLS:
- Science based university degree, preferably in MD, Ph D or PharmD
- 2+ years working experience of regulatory and drug/biologic development within a global environment in the pharmaceutical industry
- Excellent knowledge of regulatory submission and approval processes in one or more major regions
- Expertise in HA negotiations as well as a solid understanding of post-marketing/brand optimization strategies and commercial awareness
- Languages: fluent English both written and spoken
YOUR TASKS:
- Liaising with some independence under limited supervision to provide strategic and operational regulatory direction as well as supporting the DRA global program team
- Ensuring the execution of regulatory plans in line with global regulatory strategy in close collaboration with the DRA GPT representative
- Specifying requirements and setting objectives for Health Authority (HA) interactions with GPRD
- Collaborating with HAs as appropriate in meetings with GPRD as well as coordinating and planning rehearsals for HA meetings
START: ASAP
DURATION: 10MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12476
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND?
In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
YOUR EXPERIENCE/SKILLS:
- Science based university degree, preferably in MD, Ph D or PharmD
- 2+ years working experience of regulatory and drug/biologic development within a global environment in the pharmaceutical industry
- Excellent knowledge of regulatory submission and approval processes in one or more major regions
- Expertise in HA negotiations as well as a solid understanding of post-marketing/brand optimization strategies and commercial awareness
- Languages: fluent English both written and spoken
YOUR TASKS:
- Liaising with some independence under limited supervision to provide strategic and operational regulatory direction as well as supporting the DRA global program team
- Ensuring the execution of regulatory plans in line with global regulatory strategy in close collaboration with the DRA GPT representative
- Specifying requirements and setting objectives for Health Authority (HA) interactions with GPRD
- Collaborating with HAs as appropriate in meetings with GPRD as well as coordinating and planning rehearsals for HA meetings
START: ASAP
DURATION: 10MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12476
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND?
In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung, Marketing/Vertrieb