Glp Study Director
Vor 4 Tagen
Celerion Switzerland AG is part of the global Celerion Inc. With our European GLP-certified bioanalytical facility located in Fehraltorf / Zürich, as a contract research organization (CRO) we are supporting the pharmaceutical and biotechnology industries during the development of new drugs and products.
Due to the continued expansion of our successful bioanalytical laboratory we are looking for a
**GLP Study Director / Bioanalytical Principal Investigator LBS (100%)**
**Main responsibilities**
- Conduct of bioanalytical studies and bioanalytical method validations
- Primary study contact for our clients
You will be the single point of study control and have the full responsibility for the conduct of the study or study phase. You will be the responsible person to issue a study plan, organize the practical work in the laboratory, ensure that the study plan is followed and all analytical data generated are fully documented and recorded. You provide proper training of assigned personnel, review and assess all data generated and issue and approve the analytical report. You will be the main contact person for your assigned clients, provide regular updates and maintain close communication lines.
JOB REQUIREMENTS
**Our requirements**
- A minimum of 3 years practical experience within the area of bioanalysis or quantitative analysis using Ligand Binding Assays (EIA, RIA) or/and within the area using LC-MS / MS, ideally within a GLP/GMP-regulated environment
- Excellent oral and written communication skills in English and at least good skills in German
- High degree of self-motivation, commitment, reliability and flexibility to provide superior service for our clients
**Our offer**
- Responsible role within a dynamic team
- Competitive salary
- Comprehensive training into your role and responsibilities
- Opportunity to work on a variety of challenging projects in a state-of-the-art equipped laboratory
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