Non-clinical Study Coordinator

vor 2 Wochen

Basel, Schweiz Idorsia Pharmaceuticals Ltd. Vollzeit

**About Idorsia Pharmaceuticals Ltd**

Idorsia Ltd is reaching out for more - We have more ideas, we see more opportunities and we want to help more patients.
In order to achieve this, we want to develop Idorsia into one of Europe’s leading biopharmaceutical companies, with a strong scientific core.
Headquartered in Switzerland - a European biotech hub - Idorsia is specialized in the discovery and development of small molecules, to transform the horizon of therapeutic options. Idorsia has a broad portfolio of innovative drugs in the pipeline, an experienced team, a fully-functional research center, and a strong balance sheet - the ideal constellation to bringing R&D efforts to business success.
Idorsia was listed on the SIX Swiss Exchange (ticker symbol: IDIA) in June 2017 and has over 1,000 highly qualified specialists dedicated to realizing our ambitious targets.

**Responsibilities**:

- Review, track and file documents such as quotations, protocols, draft reports, final reports and other toxicity study-related documents electronically and in paper format
- Overview of all secrecy agreements and MSAs concerning Toxicology and DM/PK
- Liaise with legal and global procurement in matters of MSAs, secrecy agreements
- Inform and communicate with all internal and external parties in order to initiate and smoothly run the studies
- Oversee all aspects of study compliance with regards to study protocol and stated timelines
- Assist with essential logistics, documentation and materials required for study initiation
- Provide administrative support in the management of incoming and outgoing correspondence
- Support GLP Lab with QC checks
- Assist with budget planning
- Execute financial procedures like purchase orders, invoicing and accruing, contracts within the preclinical development field using the internal tools
- Support of toxicology group with regards to internal infrastructure
- Communication with external providers to organize the Toxicology studies and get the required timeslots for the studies
- Take responsibility of assigned new processes, develop them and present them to the team
- Commercial education with several years of working experience
- At least 3 years of work experience in a life science field
- Fluent in written and spoken English, German is an asset
- Strong interpersonal and communication skills internally and externally
- Excellent organizational skills and attention to detail
- Proven ability to work independently, take directions from various sources and prioritize workload in order to meet deadlines
**What Idorsia offers**
- Exciting opportunities for development and professional growth within our dynamic organization
- A collaborative and solution-oriented environment where you can make a difference
- An innovative and open culture in a truly multicultural environment
- A competitive salary and generous social benefits
**Work Location**: Allschwil - Basel Area
**Country**: Switzerland
**Business Area**:Preclinical Development
**Schedule**: Full-time

**Job Type**:Permanent
**Job ID**:3308

**Job Types**: Full-time, Permanent

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