Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Clinical Trial Associate
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Support, Client
Projektbeschreibung
Clinical Trial Associate wanted for our Basel based client in the pharmaceutical industry.
YOUR EXPERIENCE/SKILLS:
- Science based university degree or relevant work experience in life sciences or nursing
- Practical experience in document management, preferably within clinical trails
- Constitutive knowledge of regulatory requirements and pharmaceutical development
- Ability to work in a team together with outstanding organizational skills
- Languages: fluent English both written and spoken
YOUR TASKS:
- Assisting the operational and logistical aspects of clinical trials according to ICH-GCP
- Supporting the Clinical Trial Leader (CTL) with many of the tasks involved with the smooth running of clinical trials
- Preparing clinical, regulatory and study-related essential documents such as study protocols, case report forms and informed consent forms
- Collaborating with contract organizations, vendors and other suppliers of project support services to ensure study deliverables are met
- Ensuring accuracy of clinical trial management databases and resource tracking tools
- Coordinating internal CTL meetings or external investigator meetings as well as maintaining knowledge and training of ICH-GCP, current regulations and procedures
START: 05/2018
Duration: 17MM+
Location: St. Johann, Switzerland
Ref.Nr.: BH12628
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 or relevant work experience in life sciences or nursing
- Practical experience in document management, preferably within clinical trails
- Constitutive knowledge of regulatory requirements and pharmaceutical development
- Ability to work in a team together with outstanding organizational skills
- Languages: fluent English both written and spoken
YOUR TASKS:
- Assisting the operational and logistical aspects of clinical trials according to ICH-GCP
- Supporting the Clinical Trial Leader (CTL) with many of the tasks involved with the smooth running of clinical trials
- Preparing clinical, regulatory and study-related essential documents such as study protocols, case report forms and informed consent forms
- Collaborating with contract organizations, vendors and other suppliers of project support services to ensure study deliverables are met
- Ensuring accuracy of clinical trial management databases and resource tracking tools
- Coordinating internal CTL meetings or external investigator meetings as well as maintaining knowledge and training of ICH-GCP, current regulations and procedures
START: 05/2018
Duration: 17MM+
Location: St. Johann, Switzerland
Ref.Nr.: BH12628
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, Sonstiges