Senior Research Scientist hos Camurus i Lund
Utvecklar toxikologiska strategier och koordinerar externa toxikologiska studier. Kräver PhD eller MSc i toxikologi, farmakologi eller annat relevant Life Science-ämne samt erfarenhet av icke-klinisk läkemedelsutveckling och GLP-studier. Kräver flytande engelska.
Titel, arbetsplatsens namn och sammanfattning skrivna av AI utifrån annonsen.
Bra att veta
Lön
Inom yrkesgruppen Civilingenjörsyrken inom kemi och kemiteknik har de som jobbar i privat sektor i Sydsverige i snitt 53 800 kr i månaden, varav 53 100 kr i grundlön. I hela landet, i privat sektor, tjänar hälften mellan 44 100 kr och 59 800 kr. Det är statistik för yrket, inte vad den här arbetsgivaren betalar.
Källa: SCB, lönestrukturstatistik 2025
Anställningen
Anställningen har inget slutdatum. Den kan börja med en provanställning på högst sex månader. Vill arbetsgivaren avsluta den under provtiden ska du få besked minst två veckor i förväg; annars blir den en vanlig tillsvidareanställning när provtiden är slut. Därefter krävs sakliga skäl för att säga upp dig, och uppsägningstiden är minst en månad, längre ju längre du har varit anställd.
Annonsen kommer från ett bemannings- eller rekryteringsföretag. Det framgår inte om du anställs av företaget eller av en kund; det är bra att fråga om.
Ett kollektivavtal kan ge andra regler än lagen.
Texten är skriven med AI och kan innehålla fel. Kontrollera med arbetsgivaren.
Källa: Lagen om anställningsskydd (LAS)
Arbetsgivaren
TOBLOR Consulting har annonserat 13 jobb det senaste året: 13 tillsvidareanställningar. Det är deras första annons inom yrkesgruppen Civilingenjörsyrken inom kemi och kemiteknik på två år.
Källa: vår sammanställning av Arbetsförmedlingens annonser
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.
We are looking for an experienced Senior Research Scientist, Toxicology to join our Non-Clinical Development team.
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:
- Develop toxicology strategies and non-clinical development plans.
- Design and monitor outsourced GLP studies.
- Select, manage and collaborate with international CRO partners.
- Prepare and review toxicology reports and regulatory documentation.
- Represent Non-Clinical Development in cross-functional development teams.
- Ensure compliance with GLP and international regulatory requirements (ICH, FDA, EMA and OECD).
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.
Camurus offers
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.
Information and application
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/.
We are looking forward to seeing your application!
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