Senior Research Scientist - Toxicology - Camurus (Lund)

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative,

long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class

potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D

pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across

Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the

ticker CAMX. For more information, visit www.camurus.com and LinkedIn.

In this role, you will join the Non-Clinical Development team in Lund and contribute to the development of innovative medicines in

a dynamic and collaborative environment. You will play a central role in the toxicological strategy for Camurus' products, working

closely with colleagues across multiple disciplines as well as external partners.

This is a strategic and cross-functional role where you will be responsible for developing non-clinical plans, designing

toxicology programs and coordinating outsourced non-GLP and GLP toxicology studies performed by Contract Research Organizations

(CROs). Acting as Sponsor Monitor, you will oversee study design, study conduct, data review and final reports, ensuring

scientific quality, regulatory compliance and timely delivery. You will also contribute to regulatory submissions by preparing and

reviewing non-clinical documentation and representing Non-Clinical Development in product development teams.

Main responsibility

Among others, your responsibilities will include:

Candidate profile

You hold a PhD or MSc in Toxicology, Pharmacology or another relevant Life Science discipline.

You have several years of experience from non-clinical drug development within the pharmaceutical, biotechnology or CRO industry.

Experience of planning, monitoring or conducting GLP toxicology studies is essential, and you are familiar with outsourced

development and regulatory requirements. Experience as a Sponsor Monitor or Study Director is highly valued.

You are an experienced scientific writer with solid knowledge of regulatory documentation. You are able to author the full range

of non-clinical documentation, e.g non-clinical overviews and summaries for regulatory submissions, and the non-clinical parts of

the Investigator’s Brochure (IB). Experience of regulatory submissions is an advantage.

As a person, you are collaborative, structured and proactive. You enjoy coordinating complex projects, building strong

relationships and working in a cross-functional, international and deadline-driven environment. Fluency in spoken and written

English is required.

This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful

in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio

in different stages, the commercial potential is considerable. The position offers an international work environment and corporate

culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will

work together with highly competent colleagues, caring for each other.

You will have a broad area of responsibility and drive multiple non-clinical programs, working closely with leading international

CROs and cross-functional development teams. With your toxicology background you will have a crucial role in R&D related

activities.

Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of

innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment.

For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone:

+46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and

personal letter. For more information about Camurus, please visit: https://www.camurus.com/.