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Process Document Manager
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Client, Support
Projektbeschreibung
Process Document Manager with profound knowledge of clinical studies wanted for our Zurich based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- 5+ years' experience in the pharmaceutical industry, preferably in Clinical Development, Quality Assurance or Vaccines
- Ability to deliver clinical studies such as ICH-GCP, study management, site management and monitoring successful
- Profound knowledge of local and international regulations and guidelines
- Strong self-organisation and time management skills as well as a structured way of working
- Languages: fluent English both written and spoken
YOUR TASKS:
- Responsible for coordinating activities and implementing actions related to the maintenance and development of high quality standards and delivery of clinical studies
- Reviewing development and implementation of global procedural documents as well as the documentation of life cycle including creating, reviewing, editing, approving, posting, tracking, maintaining and ensuring inspection readiness
- Leading and facilitating Quality Management Systems review team
- Implementing strategy on development's GxP and non-GxP training records as well as developing and planning trainings, maintaining training records and tracking training status and performances, ensuring inspection readiness
- Contributing to the implementation of Data and Learning Management Systems
- Supporting the preparation for audits and regulatory inspections and giving feedback for clinical processes and initiating change management
START: ASAP
DURATION: 9MM+
LOCATION: Zurich, Switzerland
REF.NR.: BH12610
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:
- 5+ years' experience in the pharmaceutical industry, preferably in Clinical Development, Quality Assurance or Vaccines
- Ability to deliver clinical studies such as ICH-GCP, study management, site management and monitoring successful
- Profound knowledge of local and international regulations and guidelines
- Strong self-organisation and time management skills as well as a structured way of working
- Languages: fluent English both written and spoken
YOUR TASKS:
- Responsible for coordinating activities and implementing actions related to the maintenance and development of high quality standards and delivery of clinical studies
- Reviewing development and implementation of global procedural documents as well as the documentation of life cycle including creating, reviewing, editing, approving, posting, tracking, maintaining and ensuring inspection readiness
- Leading and facilitating Quality Management Systems review team
- Implementing strategy on development's GxP and non-GxP training records as well as developing and planning trainings, maintaining training records and tracking training status and performances, ensuring inspection readiness
- Contributing to the implementation of Data and Learning Management Systems
- Supporting the preparation for audits and regulatory inspections and giving feedback for clinical processes and initiating change management
START: ASAP
DURATION: 9MM+
LOCATION: Zurich, Switzerland
REF.NR.: BH12610
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