Debiopharm is privately-owned Swiss biopharmaceutical company committed to research in Oncology and Infectious diseases to improve patient outcomes and quality of life. Debiopharm International SA aims to develop innovative therapies via our unique “development only” business model, acting as a bridge between disruptive discovery products and patient access in international markets. At Debiopharm you will be at the forefront of the fight against cancer and infectious diseases through working on innovative medicines for patients. Efficacy is our mode of action, saving lives our collective target. Join our team at Debiopharm where together, we innovate, we impact, and we grow.

For our Clinical Pharmacology & Pharmacometrics Unit organization based at our Headquarters in Lausanne, we are looking for a

Principal Clinical Pharmacologist

In this role, you will be the leader for developing the clinical pharmacology scientific strategy for assigned projects in Oncology and/or Infectious diseases. To that aim, you will manage, conduct and supervise clinical pharmacology activities to add value, support, and accelerate the development of Debiopharm’s innovative medicine.

Requirements

Your responsibilities will be but not limited to:

·        Work in close collaboration with the project team and develop the clinical pharmacology strategy for assigned projects in Oncology or Infectious diseases

·        Manage the clinical pharmacology activities of assigned projects, by contributing to the design of clinical pharmacology studies (SAD/MAD PK, bioequivalence, food effect, drug-drug inter- actions, PK in special populations, …)

·        In collaboration with the pharmacometricians, elaborate the pharmacometrics strategy and organize the pharmacometrics activities for the assigned projects

·        Be a member of the Clinical Trial team, contribute to the protocol writing and manage the PK and PK/PD analyses (noncompartmental analyses and modeling approaches) and reporting; manage the risk of food-drug interactions and drug-drug interactions regarding concomitant medications.

·        Manage the outsourced activities, from provider selection until completion of project

·        Prepare the clinical pharmacology and pharmacometrics documentation to support regulatory or other cross-functional activities; may participate in interactions with Health Authorities

·        Contribute and participate to scientific communication and events

·        As part of Debiopharm’s model, contribute to the In & Out licensing activities or external fund- raising activities

Benefits

Your profile

·        PhD (PharmD is a plus) in Life sciences, pharmacokinetics, clinical pharmacology, or a related discipline

·        At least 7-year experience in clinical pharmacology within Translational R&D and early clinical phases of drug development

·        Expertise in Pharmacometrics such as Non-Compartmental PK analysis, Population PK/PD, Modeling & Simulation

·        Excellence knowledge of GCP, GCLP, GLP, and relevant regulatory guidelines

·        Experience in Antibody Drug Conjugate development is an asset

·        You are used in working in cross-functional team and fast-paced environment

·        Team player, looking to tackle challenges together with your team

·        Excellent communication skills in English (oral and written), French is an asset

Debiopharm can offer you

·        An international and highly dynamic environment, with a long-term vision.

·        The opportunity to join a successful company, at the forefront of the most advanced scientific developments in the industry and be exposed to many areas within clinical development and the pharmaceutical industry.

·        The possibility of being in a company in which innovation, people and entrepreneurship are the fundamentals of its success.

We do not accept unsolicited applications from agencies or recruiters.