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Principal Scientist/Study Director (Colleretto Giacosa, Turin, IT, 10010) @ SUSONITY

Colleretto Giacosa, Turin, IT, 10010OnsiteFull-time
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About this role

<p style="text-align:justify"> </p> <p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif">Work Your Magic with us! </span></span></p> <p> </p> <p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif">Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That&apos;s why we are always looking for curious minds that see themselves imagining the unimaginable with us. </span></span></p> <p> </p> <p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif">United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.</span></span></p> <p style="text-align:justify"> </p><h2><span style="font-size:12.0pt;font-family:verdana, geneva, sans-serif">Your Role</span></h2> <p><span style="font-size:12.0pt;font-family:verdana, geneva, sans-serif">You will manage and coordinate preclinical safety, pharmacokinetic, and toxicology studies in rodent and non-rodent species. As a Study Director or Responsible Scientist, you are accountable for the entire study lifecycle, from initial planning and protocol preparation to the scientific evaluation and interpretation of experimental data. You will perform essential in vivo tasks, including treatments, biological sample collection, and clinical observations, while conducting diagnostic and instrumental evaluations. Your responsibilities extend to monitoring outsourced preclinical studies at CROs to ensure quality and compliance. You will develop new experimental methods, coordinate inter-laboratory activities, and draft operational procedures. Furthermore, you support technical staff training and actively contribute to animal welfare standards to ensure the highest level of research integrity.</span></p> <p> </p> <h2><span style="font-size:12.0pt;font-family:verdana, geneva, sans-serif">Who You Are</span></h2> <ul> <li style="font-size:12.0pt;font-family:verdana, geneva, sans-serif"><span style="font-size:12.0pt;font-family:verdana, geneva, sans-serif">Degree in Veterinary Medicine, Biology, or a related scientific field.</span></li> <li style="font-size:12.0pt;font-family:verdana, geneva, sans-serif"><span style="font-size:12.0pt;font-family:verdana, geneva, sans-serif">Proven experience as a Study Director in toxicology and PK studies.</span></li> <li style="font-size:12.0pt;font-family:verdana, geneva, sans-serif"><span style="font-size:12.0pt;font-family:verdana, geneva, sans-serif">Deep expertise in GLP and GRP regulations and their application.</span></li> <li style="font-size:12.0pt;font-family:verdana, geneva, sans-serif"><span style="font-size:12.0pt;font-family:verdana, geneva, sans-serif">Skilled in in vivo techniques, sampling, and clinical observations.</span></li> <li style="font-size:12.0pt;font-family:verdana, geneva, sans-serif"><span style="font-size:12.0pt;font-family:verdana, geneva, sans-serif">Background in monitoring outsourced studies and managing CROs.</span></li> <li style="font-size:12.0pt;font-family:verdana, geneva, sans-serif"><span style="font-size:12.0pt;font-family:verdana, geneva, sans-serif">Strong ability to draft reports and standard operating procedures.</span></li> <li style="font-size:12.0pt;font-family:verdana, geneva, sans-serif"><span style="font-size:12.0pt;font-family:verdana, geneva, sans-serif">Commitment to high animal welfare and ethical research standards.</span></li> </ul><p> </p> <p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif"><strong>What we offer:</strong> We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!</span></span></p> <p> </p> <p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif">Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!</span></span></p>

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