Job Information
Boehringer Ingelheim Senior Clinical Scientist in Rohrdorf, Germany
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 is part time eligible with 90 %.
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) please use this link: https://jobs.boehringer-ingelheim.com/job-invite/13019/
If you want to apply for the position in the USA (Fulton) please use this link: https://jobs.boehringer-ingelheim.com/job-invite/13173/
If you want to apply for the position in Germany (Rohrdorf) 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!
Tasks & 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 of veterinary medicine strongly preferred from an accredited institution with previous experience in antiparasitic product Development or PhD or Master’s 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
Ready to contact us?
If you have any questions about the job posting or process – please contact our HR Direct Team,
Tel: +49 (0) 6132 77-3330 or per mail: hr.de@boehringer-ingelheim.com
Recruitment process:
Step 1: Online application – application deadline is July 5th, 2024.
Step 2: Virtual meeting starting at the beginning of July 2024.
Step 3: On-site interviews start at the end of July 2024 (candidates from the US and France will have virtual interviews instead).
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.