Senior Scientist, Translational PK & Oncology – Hybrid Turku

Orion Pharma

Turku

Hybrid

EUR 90,000 - 120,000

Full time

14 days+
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Job summary

Orion Pharma in Turku, Finland, seeks a Senior Scientist to advance oncology drug candidates from discovery toward clinical development, focusing on PK and translational pharmacology within Translational Pharmacology. You will design and interpret nonclinical studies, contribute to dosing strategies, and prepare regulatory documents, collaborating with CROs and internal teams in a hybrid work setting.

The role offers opportunities to guide development decisions and to work with global experts

Qualifications

  • PhD/PharmD/MSc in pharmacology or related field.
  • ≥5 years biotech/pharma experience with drug discovery or development.
  • Hands-on experience in pharmacology, biology, translational pharmacology, nonclinical development, PK/DMPK or clinical pharmacology.
  • Experience designing and interpreting nonclinical studies or complex datasets supporting drug discovery or development.

Responsibilities

  • Provide PK and translational pharmacology expertise to R&D projects from discovery toward clinical development.
  • Design, monitor, interpret and report nonclinical PK and translational studies including CROs.
  • Analyze PK data and integrate exposure with pharmacology, safety and bioanalytical results to support project decisions.
  • Contribute to translational strategies, human dose projections, exposure‑response assessments and regulatory documents.

Skills

Multidisciplinary collaboration
English communication

Education

PhD, PharmD or MSc in pharmacology
Biochemistry/biomedical sciences background

Tools

PK/PD modelling tools
Bioanalytical software

Job description

Orion Pharma in Turku, Finland, seeks a Senior Scientist to advance oncology drug candidates from discovery toward clinical development, focusing on PK and translational pharmacology within Translational Pharmacology. You will design and interpret nonclinical studies, contribute to dosing strategies, and prepare regulatory documents, collaborating with CROs and internal teams in a hybrid work setting.

The role offers opportunities to guide development decisions and to work with global experts

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