Senior Non-Clinical Project Manager - Unique Human Capital

Make a tangible impact for people with metabolic and neurologic disease
As Senior Non-Clinical Project Manager at Gubra, you will join a growing development team as the primary toxicologist. You’ll play a pivotal role in establishing workflows, building internal and external networks, and fostering cross-functional collaborations. This position offers significant personal development opportunities, including leading major initiatives, shaping your role, and taking on exciting projects as the pipeline evolves.

You will drive the peptide drug candidates' non-clinical safety and toxicology activities in collaboration with the development project team and external partners and participate in authority meetings.

Your main tasks are:

• Formulate and lead preclinical safety strategies and activities.
• Overall scientific and project management of non-clinical activities and studies.
• Act as subject matter expert and lead on toxicology matters for ongoing portfolio programs.
• Contribute to the overall scientific strategy and product pipeline and give in-depth scientific advice on potential new projects.
• Ensure compliance with regulatory trends and guidelines

Your qualifications include several years of experience in toxicology, specialising in peptides and/or biologics within the pharma/biotech industry or a CRO in a GLP setting. You have proven experience working with CROs and regulatory authorities, and pharmacology experience is a plus.

You have a Master’s Degree in biology, Human Biology, DVM, or similar scientific education.

You are self-driven and motivated, taking full ownership of your work and thrive in a dynamic, entrepreneurial environment. You excel in teamwork, value autonomy, and know when to seek expert advice. Strong project management skills allow you to juggle multiple tasks while staying organised and efficient. Critical thinking, problem-solving, and attention to detail are essential, as is maintaining high ethical standards and prioritising quality.

Gubra offers an exciting and challenging work environment where job satisfaction and personal development are top priorities. Gubra’s ambition is to provide a collaborative workplace where talented people are empowered to use their competencies and passions every day. The team works together to make a positive impact on people’s lives.

Travelling: Limited.

Domicile: Gubra’s facility in Hørsholm.

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Gubra, founded in 2008 in Denmark and listed on NASDAQ Copenhagen, specialises in pre-clinical contract research services and peptide-based drug discovery within metabolic and fibrotic diseases. Gubra’s activities are focused on the early stages of drug development and are organised in two business areas – CRO Services and Discovery & Partnerships (D&P). The two business areas are highly synergistic and create a unique entity capable of generating a steady cash flow from the CRO business while at the same time enjoying biotechnology upside in the form of potential development milestone payments and potential royalties from the D&P business. In 2023, Gubra had approx. 220 employees and revenue of DKK 205 million.

Read more at http://www.gubra.dk

Adresse:
Hørsholm, Denmark