CDI - Senior Principal Scientist pharmacologisttoxicologist
CDI - Senior Principal Scientist pharmacologisttoxicologist
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Job Description
Ensure the role of Pharmacology and Toxicology expert: involved in earlystage projects (preprojects) propose actions to evaluate and select them participate proactively in the conception of project development plans and define the rationale evaluate acquisition opportunities assess scientific communications and give guidance and support for the different studies carried out to fulfill screening and development needs. Support Vetoquinols global strategy.
Represent the Preclinical and Clinical Department within the Project Team as a Project Team Member. Coordinate and ensure implementation of the defined actions for product development. These actions must be determined in respect of the Target Product Profile in compliance with external constraints (regulations customer expectations) and internal constraints (resources and deadlines) and comply with the development plan.
As an Expert in Pharmacology and Toxicology you will:
- Establish strategic recommendations in support of preprojects in your field of expertise (identification of issues analysis of possible options / rational selected)
- Recommand essential studies to confirm interest/validity of selected preprojects contribute to their experimental design analysis and interpretation of the results and to the conclusion give your recommendation for the outcome of the preproject
- Participate in evaluating development opportunities (due diligence) and establish recommendations based on a synthesis of the data reviewed
- Contribute to the evaluation of research program opportunities and make recommendations
- Contribute to the definition of the development plan for Safety and Efficacy sections in terms of studies and resources to achieve the validated Target Product Profile for all projects
- Advise and support Study Managers in the conception and design of pharmacotox studies and if necessary review the study reports
- Establish the strategy to answer the questions within the Pharmacology and Toxicology fields both internally (Research & IP Marketing & Medical Regulatory Affairs... and externally (Regulatory Authorities)
- Participate in the resolution of technical or experimental problems by establishing where appropriate investigation plans
- Set up/animate and maintain a network of experts/researchers in Pharmacology and Toxicology
As a Project Team Member contribute to the projects under your responsibility:
- Define and propose the development plan for Safety and Efficacy sections in terms of studies and resources to achieve the validated Target Product Profile in collaboration with any other relevant contributor before validation by the Director of the Department
- Coordinate the actions of the development plan within the Preclinical and Clinical (PCC) Department ensure they are executed within the defined time coordinate the corrective actions to achieve the established critical milestones and keep the Project Team informed
- Ensure communication and flow of information between the Project Team and the Team Managers (leaders) of the PCC Department
- Contribute to the transcription of desired attributes of the Target Product Profile into target SPC and update them according to the project data
You will also contribute to Scientific Communication Scientific Intelligence Group Image and Innovation:
- Participate in scientific communication inside and outside the Vetoquinol Group to share information within the different Departments and develop Vetoquinols image externally
- Participate in/lead working groups of multidisciplinary experts aimed at enhancing the interests of Vetoquinol
- Participate in conventions and monitor scientific literature in line with the Vetoquinol strategy to stay uptodate with current knowledge in Pharmacology and Toxicology and identify scientific advances of interest. Establish recommendations on competitive and technological advantages and promote their
- Contribute to the representation and defense of the Group at professional (Animal Health Europe CEESA SIMV and expert organizations (e.g. EAVPT ECVPT ACVCP AAVPT ABVT) or through professional events (publications conferences)
Qualifications :
Qualifications
You have a scientific doctorate level education with a Pharmacology and/or Toxicology specialty and you have 10 years of experience in drug development. You master dedicated IT tools (e.g. Phoenix NONMEM Monolix). You are fluent in English knowledge of French an asset (Headquarters in Eastern France).
You are open minded and collaborative. You have an analytical and rational approach and propose recommendations
You are a critical thinker with a problemsolving approach.
Additional Information :
Full time position executive status preferentially based at Company Headquarters in Eastern France 70200 MagnyVernois possible to be based at office in Paris.
You will collaborate with all Corporate Scientific Division Departments (including USA and Brazil) with Medical and Marketing Division and with external partners CROs KOLs Regulatory Authorities professional bodies (SIMV Animal Health Europe Health for Animals CEESA)
You will travel in France and internationally
Remote working 2 days/week is possible
Conditions & advantages :
Remuneration package including a fixed salary according to your profile 10 variable portion based on objectives company vehicle vacation bonus of 365 euros gross increased according to seniority in the company participation company savings plan mutual insurance/provident insurance restaurant vouchers (one per day) 13 days of RTT CSE Support in finding accommodation 50 reimbursement of public transport subscriptions Events/actions promoting wellbeing at work
Remote Work :
Yes
Employment Type :
Fulltime
Employment Type
Remote
