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Clinical Trial Supply Associate Manager
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Engineering, Client
Projektbeschreibung
Clinical Trial Supply Associate Manager wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Academic Degree in Science, Engineering or relevant field
- 2+ years of professional experience in a chemical or pharmaceutical company
- Excellent knowledge of clinical practice, clinical trials, regulatory processes (GMP, HSE)
- Basic leadership and project management skills along with presentation skills
- Strong ability working independently and within interdisciplinary teams
- Languages: fluent English both written and spoken
YOUR TASKS:
- Defining and executing an optimal clinical trial supply strategy for a clinical trial
- Conducting compliance of processes with regulations as well as internal procedures and GxP requirements
- Participating in team activities and fulfilling all related tasks and duties
- Analyzing results and data, drawing conclusions and reporting back to team and management
- Leading and supervising team members, contributing to team goals and providing technical training
- Monitoring Key Performance Indicators (KPI) and performance measures ensuring all strategic objectives are met according to timelines, budget, quality standards
START: 07/2018
DURATION: 12MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12803
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:
- Academic Degree in Science, Engineering or relevant field
- 2+ years of professional experience in a chemical or pharmaceutical company
- Excellent knowledge of clinical practice, clinical trials, regulatory processes (GMP, HSE)
- Basic leadership and project management skills along with presentation skills
- Strong ability working independently and within interdisciplinary teams
- Languages: fluent English both written and spoken
YOUR TASKS:
- Defining and executing an optimal clinical trial supply strategy for a clinical trial
- Conducting compliance of processes with regulations as well as internal procedures and GxP requirements
- Participating in team activities and fulfilling all related tasks and duties
- Analyzing results and data, drawing conclusions and reporting back to team and management
- Leading and supervising team members, contributing to team goals and providing technical training
- Monitoring Key Performance Indicators (KPI) and performance measures ensuring all strategic objectives are met according to timelines, budget, quality standards
START: 07/2018
DURATION: 12MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12803
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
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Kategorie:
IT Entwicklung, Ingenieurwesen/Technik