Description
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:
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