Toxicologist - Ivry-sur-Seine, France - Thermo Fisher Scientific

Thermo Fisher Scientific
Thermo Fisher Scientific
Entreprise vérifiée
Ivry-sur-Seine, France

il y a 1 semaine

Sophie Dupont

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Sophie Dupont

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Description
Job Description

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale.

Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.

We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.

Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.


Location/Division Specific Information:


Strategic Development Consulting (SDC) is a dynamic team of consultants that guides customers through the development and approval journey, navigating the obstacles in between.

We provide early engagement and regulatory strategy, clinical science, development consulting, and clinical pharmacology, with services spanning the full development spectrum.


We have an exciting opportunity for a Toxicologist (Associate Director) to join our team, fully dedicated to a single sponsor.

The role will work with a team that is a functional expert group within the development department with expertise in nonclinical safety testing, operations of regulated studies and nonclinical and clinical bioanalytics.

You will work closely with sponsor colleagues from other functional areas (e.g., from discovery to CMC, clinical operations and global patient safety).


Discover Impactful Work:


The toxicologists are responsible for the design of the nonclinical packages of their assigned projects to support clinical trials and worldwide registration file submissions, the commission to CRO and compliant conduct of their studies, and the correctness of the nonclinical safety sections of regulatory documents and the investigator brochure.


Keys to Success:


  • Actively contribute to the development strategy at internal multidisciplinary project/clinical team meetings.
  • Design a nonclinical safety package that supports the ambitions of the project team, obtain buy in of all stakeholders and advise on interactions with Health Authorities to secure their timely feedback.
  • Collaborate with medical writer and regulatory affairs in development of regulatory dossiers and the investigator brochure. Ensure nonclinical safetyrelated content is correct and comprehensive.
  • In collaboration with the program manager, ensure correct financial and project planning.
  • Together with Sourcing and program manager, oversee the timely commission of studies to CRO. Participate in vendor alliance governance meetings as appropriate.
  • Ensure compliant execution of studies by study monitoring either in person or with support of study monitor. Coordinate contributions of other sponsor disciplines (CMC, Bioanalytic, Pharmacokinetics, QA).
  • Collaborate with other scientific disciplines to interpret the study outcomes and present at internal multidisciplinary project teams and Governance Committees.

Education:


  • At least 58 years of relevant nonclinical (toxicology) experience, including as a toxicologist in the pharmaceutical/biotechnology industry or at a regulatory agency.
  • A broad background of nonclinical regulatory experience on products from discovery/early development through postapproval, gained from working in the pharmaceutical industry or at a regulatory agency in one of the ICH regions.
  • Toxicology certification (Diplomate, American Board of Toxicology or European Registered Toxicologist) highly desirable but not required.
  • Proven project management experience and success building relationships across a diverse stakeholder team.
  • Knowledge of ICH, FDA, and EMA guidances and GLP requirements.
  • Ph.
D degree or equivalent by experience.


Experience:


  • A solid understanding of the pharmacology and toxicology of large molecules and immunology is a must.
  • Experience in managing outsourced activities.
  • Advanced understanding of budgeting and forecasting with the ability to interpret data with attention to detail and analytical and investigative skills
  • Capable of supervising, evaluating, and mentoring departmental personnel, as well as delegating tasks and facilitating the completion of assignments

Knowledge, Skills, Abilities:


  • Superior English language communication and negotiation skills, as well as local language where applicable, both oral and written
  • Excellent understanding of global drug development throughout the product lifecycle, with emphasis on nonclinical disciplines; superior understanding of ICH and other global nonclinical regulatory guidances.
  • Capable of driving innovation in developing new ideas related to process improvements
  • Excellent organizationa
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