T2305 -non-clinical Data Manager - Translational

Description

Debiopharm is an independent biopharmaceutical company based in Switzerland with an ongoing commitment to research in oncology and infectious diseases in order to improve patient outcomes and quality of life. Our main activities include drug development, drug manufacturing and digital health investment. Debiopharm International SA aims to develop innovative therapies that target high unmet medical needs. Our unique “development only” business model allows us to act as a bridge between disruptive discovery products and patient access in international markets. We first identify high-potential compounds for in-licensing, clinically demonstrate their safety and efficacy and then select large pharmaceutical commercialization partners to maximize patient access globally.

At Debiopharm you will be at the forefront of the fight against cancer and infectious diseases, and you will have the opportunity to work on new innovative medicines for patients. Efficiency is our mode of action, saving lives our collective target.

For our Data Management organization based at our Headquarters in Lausanne, we are looking for a

Non-clinical Data Manager - Translational Medicine

(12 months contract)

In this project role, you ensure the data flow management from non-clinical produced by our Translational Medicine Department, from data ingestion to Central data repository to harmonization in Genedata platform, and support the internal decision-making process.

You will be a member of the project team Genedata, and will contribute to the platform deployment & related process development in compliance with SOPs and regulatory guidelines.

**Your responsibilities will be but not limited to**:
**Contribute to the Platform development**:
data flow set up and automations
integration with Central Data Repository (from business side)
Ensure non-clinical data ingestion for projects with a first focus for new and ongoing projects
Ensure data mapping, harmonization based on Translational Medicine (TM) specifications
Prepare standard Data Transfer Specifications in collaboration with TM team
Develop Data Management related processes linked to the Platform
Ensure the link between Translational Team and Clinical data management for Central Data Repository initiatives

**Requirements**:
Master or PhD in Science required, additional training in bioinformatic is a plus
First experience with non clinical activities and related data (ADME, DM-PK, pharmacology, toxicology, biomarkers (-omics data), )
Experience of 2 years minimum in data management area within the pharmaceutical industry (sponsor or CRO)
Efficient planning, organizational and communications skills to run projects against deadlines
You are solution-oriented and passionate by Sciences
Ability to effectively work and collaborate in a complex matrix organization.
Fluent in English, good knowledge of French is an asset

**Benefits**:
Possibility to work from home with weekly visit in the office (Lausanne)
The opportunity to join a successful company, at the forefront of the most advanced scientific developments in the industry and be exposed to many areas within clinical development and the pharmaceutical industry
The possibility to be in a company in which innovation, people and entrepreneurship are the fundamentals of its success
Proud to be an Equal-Pay certified, we ensure offering to all our employees the same opportunities

Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external staffing agency or recruiter does not create any implied obligation on the part of Debiopharm.

**Job Type**: Contract