Preclinical PKPD Scientist (Client dedicated), EMEA

Brussels - Belgium

Monthly Salary: Not Disclosed

Posted on: 2 days ago

Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as Principal Pharmacokineticist Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 countries in the last 5 years.

As part of our expert team youll have the opportunity to ensure operational excellence that makes a real difference in clinical pharmacology. You will guide design of nonclinical studies (PK TK PKPD) translational PKPD analysis in collaboration with the clinical Pharmacologist support the bioanalytical scientist in strategic and operational planning of nonclinical and early clinical work.

What Youll Do:

Is responsible for managing and safeguard nonclinical PKPD data

Interacts and discusses data and strategies with stakeholders and vendors for PKPD analysis

Advises and sets up adequate software infrastructure in collaboration with IT

Discusses development strategies with technical and cross-functional teams and advises on design of nonclinical studies including GLP toxicology studies

Reviews study reports including Toxicokinetic phase reports

Processes and models data using appropriate software (such as Phoenix WinNonlin R)

Reports results to nonclinical pharmacology and bioanalytical team cross-functional teams and management

Prepares documents to a quality standard required for Regulatory/Health Authority submissions

Interacts with internal stakeholders to understand different project requirements and ensures timely open and effective communication to relevant stakeholders (teams collaborators management)

Applies model informed drug development (MIDD)

Education and Experience Requirements:

Advanced degree (Master or PhD) in a scientific discipline with a strong mathematical component or equal by experience

PKPD modelling experience in translational and early phases of development. Experience in different disease areas is a plus

Knowledge Skills and Abilities:

Basic understanding of GLP requirements for nonclinical safety studies

Knowledge of regulatory requirements to characterize the nonclinical pharmakinetics and safety of new biologic entities and how to propose and justify human starting doses

Strong communication skills

Strong collaborative and interpersonal skills

Problem solving skills

Fluent in English

Why Join Us

When you join Thermo Fisher Scientific you become part of a global team that values passion innovation and a commitment to scientific excellence. Youll work in an environment where collaboration and development are part of the everyday experienceand where your contributions truly make a difference.

Apply today to help us deliver tomorrows breakthroughs.

Required Experience:

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as Principal Pharmacokineticist Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 cou...