Senior Clinical Scientist (M/F) in Saint Vulbas, France

SENIOR CLINICAL SCIENTIST (H/F) en CDI

THE POSITION

Join our dynamic team as a key clinical driver in Antiparasitics, where you will be at the forefront of new animal development projects, ensuring safety and efficacy in target species.

This role offers the opportunity to shape clinical study design, manage resources and budgets, and contribute to the maintenance and extension of our existing licensed products in parasitology. You will be instrumental in guiding projects from protocol to execution, and ultimately to final study report for submission to regulatory agencies, in both lab and field conditions.

This position can be filled in Germany (Rohrdorf), USA (Fulton) or France (Saint Vulbas).

If you want to apply for the position in France (Saint Vulbas) click “Apply now”*.

We kindly ask you to apply for the Boehringer Ingelheim location that is closest to your country of residence. Please, do not apply for more than one location!

* Upon applying for this position, you will encounter a query regarding the visibility of your profile – whether it should be confined to the recruiters managing the jobs you apply to, or be accessible to any company recruiter worldwide. Given that the hiring manager is not based in the country you are applying for, we kindly urge you to opt for “Any company recruiter worldwide”. This action will greatly assist us in processing your application in the most efficient manner, while ensuring compliance with the General Data Protection Regulation.

Tasks and Responsibilities

• In your new role, you will lead Clinical Teams as Clinical Project Lead and will support the development and implementation of the clinical strategy for efficacy and safety of antiparasitic product development (from start of development to post approval support).

• Furthermore, you will ensure that clinical projects have optimal strategy, efficient study design, evaluated according to state-of-the-art principles and are properly presented.

• You will de-risk projects, characterize the salient health risks and support optimization of formulations for safe and efficacious products and support local and international regulatory submissions, and the maintenance and growth of existing products.

• Moreover, you will be responsible for the presentation of clinical content to regulatory authorities as required and ensures compliance with all applicable regulatory and animal welfare principles.

• Finally, you will act as the clinical project representative in governance meetings and organizational bodies to align clinical plans with company strategies and support clinical site study activities.

Requirements

• Doctor in Veterinary Medicine strongly preferred from an accredited institution with previous experience in antiparasitic product Development or PhD or Masters Degree from an accredited institution with experience in parasitology

• Knowledge of regulatory requirements (e.g. FDA, EMA) and compliance

• Solid understanding of claim structure of veterinary antiparasitic products

• Experience with planning, conducting, reporting, analyzing and interpreting of clinical studies

• Previous experience with clinical laboratory and/or field studies (GxP and non-GxP) is a plus

• Clinical veterinary practice experience is a plus to support site study activities

• Team player with excellent communicational skillset to effectively work in an international and cross-functional matrix environment

All qualified applicants will receive consideration for employment without regard to a person’s actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.