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Metadata Business Lead
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Support, Client
Projektbeschreibung
Metadata Business Lead wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Experience in Data Management or Clinical Trial Operations with a clear understanding of clinical data from internal and external sources
- Demonstrated knowledge of metadata management, pharmaceutical industry standards (CDISC) and regulatory requirements supporting clinical trials and submissions
- Background in managing projects and cross-functional teams as well as building successful relations with suppliers, customers and stakeholders
- Strong communication and negotiation skills that can support continuous progress
- Languages: fluent English both written and spoken
YOUR TASKS:
- Data modelling with respect to clinical data standards metadata as well as applying GxP systems development methodologies
- Progressing CDISC aligned clinical data standards such as data review, data collection, ADAM, SDTM with a governance structure for ensuring consistency and compliance across Therapeutic Areas and with our CROs to support the exchange of data
- Leading team members within the framework of the project plan and understanding clinical development processes from protocol to submission
- Working closely with implementation support teams including database set-up, completion guidelines, CRF designers, algorithm specifications and reporting requirements
START: ASAP
DURATION: 6MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12288
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:
- Experience in Data Management or Clinical Trial Operations with a clear understanding of clinical data from internal and external sources
- Demonstrated knowledge of metadata management, pharmaceutical industry standards (CDISC) and regulatory requirements supporting clinical trials and submissions
- Background in managing projects and cross-functional teams as well as building successful relations with suppliers, customers and stakeholders
- Strong communication and negotiation skills that can support continuous progress
- Languages: fluent English both written and spoken
YOUR TASKS:
- Data modelling with respect to clinical data standards metadata as well as applying GxP systems development methodologies
- Progressing CDISC aligned clinical data standards such as data review, data collection, ADAM, SDTM with a governance structure for ensuring consistency and compliance across Therapeutic Areas and with our CROs to support the exchange of data
- Leading team members within the framework of the project plan and understanding clinical development processes from protocol to submission
- Working closely with implementation support teams including database set-up, completion guidelines, CRF designers, algorithm specifications and reporting requirements
START: ASAP
DURATION: 6MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12288
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, Sonstiges