Study Manager (f/m/d)

Study Manager (f/m/d) – GLP / in vivo safety studies/3Rs principles (Replace, Reduce, Refine) /experimental study design / nonclinical safety studies / English

Project:
For our customer a big pharmaceutical company in Basel we are looking for a highly qualified Study Manager.

Background:
In Roche’s Pharmaceutical Research and Early Development organization (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs. At pRED, we are united by our mission to transform science into medicines. Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed. This position is within Pharmaceutical Sciences, part of the Pharma Research and Early Development (pRED) organization. We closely collaborate with our therapeutic areas and functions to convert hypotheses into innovative therapeutics. This early career position is located in the Translational Safety Assessment chapter, a chapter within the Pharmaceutical Sciences function, where Toxicology and drug safety are primary focus areas.

The perfect candidate: As a drug safety or toxicology Scientist you are someone who wants to influence your own development by joining a company where you have the opportunity to pursue your interests across functions and continuously learn and innovate

Tasks & Responsibilities:
* As an early career scientist, you act as a Study Manager responsible for external preclinical safety studies, in close collaboration with other scientists
* You play an active role in planning, tracking and monitoring out-sourced in vivo and in vitro studies which support exploratory and regulatory drug development
* You work with colleagues to manage and communicate on outsourced studies that support project progression across the Roche portfolio.
* You actively contribute to team discussions, sharing your ideas, listening to others and working together to progress actions both internally and with CRO business partners
* You work with study tracking tools to manage deliverables and meet timelines

Must Haves:
* You hold a PhD or Master in Life Sciences or Veterinary Medicine or are a graduate with relevant experience You bring at least 1 year of industrial experience, ideally in regulatory Toxicology and with experience or knowledge of GLP
* You have experience of in vivo safety studies, 3Rs principles (Replace, Reduce, Refine) and experimental study design which applies to both in vitro and in vivo studies
* You are an excellent communicator with high proficiency in English, both written and spoken
* You demonstrate a collaborative mindset to improve processes and support strategic excellence
* You want to take your career to the next level, learn from experienced Study Managers and join a key scientific team in Roche
* You enjoy making things happen. Whether this be problem solving, investigating and resolving or negotiating for a pragmatic outcome.

Nice to Have:
* Ideally you should have experience in the planning, conduct and reporting of nonclinical safety studies in complex organizations e.g. within a pharmaceutical company or a contract research organization

Reference Nr.: 923083SDA
Role: Study Manager
Industrie: Pharma
Workplace: Basel
Pensum: 100%
Start: 01.02.2024
Duration: 12++ (upto 3 years)
Deadline: 15.12.2023

If you are interested in this position, please send us your complete dossier via the link in this advertisement. If this position does not fit your profile and you wish to be considered for another position directly, you can also send us your dossier via this ad or to jobs[at]itcag[dot]com.
Contact us for more information about our company, our positions or our attractive Payroll-Only programme: +41 41 760 77 01.

About us:
ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering.
We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.