In this dynamic role you will participate in the design, administration and monitoring of State of the art clinical trials. Your tasks include maintaining the monthly data generation tracker and dashboard, support for the internal teams in relation to the phase IV studies internal approvals, capturing the meeting minutes from the internal scientific committee meetings, filing / archiving of the data generation related documentation (protocols, contracts, trackers etc)., managing purchase requisitions and the access to different platforms (e.g. share point, Watchdox). Support the organization and the logistic of the internal meetings. Finally submitting the requests for the external expenses reimbursements.
flexible Administrator/Clinical Associate FDA Regulatory - Biosimilars
- KV / Büro
- Area of Zug
Within the Pharmaceutical Industry globally & successfully operating company.
Area of Zug
A dynamic working environment focusing on career opportunities where multi-cultural teams from all over the world strive the best results.
Bachelor of Science or commercial background or similar
Several years of related professional experiences within the Pharmaceutical industry or similar matrix organisations. You will need a precise and accurate working style and high detail orientation, knowledge of FDA regulatory requirements is a must. ACRP or SCORA Clinical Research Professional exam completion are considered as a plus. Strong communication skills, fluency in English, proficient computer skills (MS office). If you recognize your skillset, please send your application to Mr. Anton Witprächtiger, firstname.lastname@example.org. We look forward to hearing from you.
Englisch: Very good
As a start, this position is offering a 1 year contract until August 2021. An extension is very likely. In addition, other challenging opportunities within the growing company may arise at a later stage. Client Job Nr. BIOBJP00002269