Headquartered in Lachen near Zurich, Switzerland, the Octapharma Group is a leading company in the worldwide market for therapeutic human proteins. Working at Octapharma means to have an opportunity to contribute to our common goal – developing lifesaving therapies to improve patients’ lives.
We are seeking
A Clinical Trial Associate/Clinical Documentation Specialist reporting directly to the Vice President Clinical R&D Haematology.
Set up and maintenance of Trial Master Files and Investigator Site Files
Prepare, distribute and archive clinical documentation
Manage the administrative parts of clinical trials and provide support to the Clinical Research team throughout the complete conduct of the study by documenting information such that it is always complete, up to date and available to team members and auditors
The ideal Candidate
Biological and/or clinical science or nurse/study nurse backgroun
Minimum of 2 years experience as Clinical Trial Associate or Clinical Trial Documentation Specialist in clinical research within a CRO, a pharmaceutical or a biotechnology company
Computer literate - excellent command of Word, Excel and Powerpoint
A flexible attitude with respect to work assignments
Good interpersonal and communication skills
Very detail oriented
Familiar with structure and organization and archiving of paper and electronic CRFs
Comfortable with repetitive work
Good team player
Able to manage multiple and various tasks with positive attitude
Able to prioritize workload with attention to detail and within timelines
Self starter requiring minimal supervision
Fluent in both written and spoken English; preferably also in German
- Working in a motivated team in an international environment
- Active participation in the conduct of global clinical projects
How to apply
Please apply online in English describing your interest, expected salary and enclosing your CV, references and/or recommendation letters.