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Trial Manager
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Design, Client
Projektbeschreibung
Trial Manager wanted for our Basel based client in the pharmaceutical industry.
YOUR EXPERIENCE/SKILLS:
- Working experience in a similar role accompanied with mandatory pharma knowledge
- Extensive SAP experience especially in DSM
- Ability to communicate with different levels of the organization as well as profound project and stakeholder management knowledge
- Languages: fluent English both written and spoken
YOUR TASKS:
- Coordinating trial deliverables within DSM and all other relevant associated functions and ensuring that a trial-level project plan is developed together with all relevant roles and progress of deliverables are adequately tracked
- Supervising and reviewing clinical trial protocols and protocol amendments and providing input to drug supply sections
- Developing optimal package design to match the study design and a supply plan optimized for cost, feasibility and overage
- Cooperating with Clinical Supply Documentation Specialist (CSDS) to define an optimal label strategy according to study design, study timelines, participating countries and regulatory requirements
- Managing shelf life planning on clinical finished good level and extensions of expiry dates and executes against plan to ensure supply continuity
START: ASAP
DURATION: 12MM+
LOCATION: Basel, Switzerland
REF.NR.: BH10545
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:
- Working experience in a similar role accompanied with mandatory pharma knowledge
- Extensive SAP experience especially in DSM
- Ability to communicate with different levels of the organization as well as profound project and stakeholder management knowledge
- Languages: fluent English both written and spoken
YOUR TASKS:
- Coordinating trial deliverables within DSM and all other relevant associated functions and ensuring that a trial-level project plan is developed together with all relevant roles and progress of deliverables are adequately tracked
- Supervising and reviewing clinical trial protocols and protocol amendments and providing input to drug supply sections
- Developing optimal package design to match the study design and a supply plan optimized for cost, feasibility and overage
- Cooperating with Clinical Supply Documentation Specialist (CSDS) to define an optimal label strategy according to study design, study timelines, participating countries and regulatory requirements
- Managing shelf life planning on clinical finished good level and extensions of expiry dates and executes against plan to ensure supply continuity
START: ASAP
DURATION: 12MM+
LOCATION: Basel, Switzerland
REF.NR.: BH10545
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, Medien/Design