Pharmacist, Chemist - Drug Metabolism & Pharmacokinetics (m/f/d)

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The NUVISAN Group is an internationally successful Contract Research Organisation (CRO) which performs drug trials for international pharmaceutical companies, biotech and generic manufacturers.
A complete range of clinical drug development services can be offered as a package including bioanalytics, bio pharmaceuticals, pharmaceutical analysis, stability testing and clinical trial manufacturing and packaging.
Founded in Germany in 1979, NUVISAN’s 420 highly qualified staff provide analytics and clinical studies sponsored by the pharmaceutical industry.
We are expanding our team in Grafing and are looking for an
IN-VIVO DMPK SCIENTIST - LAB LEADER (f/m/d)
Associate Director level
We are looking for a highly motivated PhD scientist as in-vivo DMPK EXPERT, associate director level, to join our Nuvisan DMPK team in Grafing near Munich. You will act as DMPK Expert/Study Director for our in-vivo DMPK studies and provide DMPK expertise to our client drug development plans. Together with management you will develop the Grafing site into a leading European non-clinical DMPK service organization. If you are someone with excellent experiences in in-vivo DMPK, conducting this role might be a great opportunity for you.
Leading a non-clinical in-vivo DMPK team consisting of lab-heads and bench scientists
Organizing, coordinating, and controlling work within your team in order to ensure optimal employment of resources
In the role of Study Director / Principal Investigator take responsibility for planning, performance, evaluation, and reporting of in-vivo studies during drug discovery and development in suitable quality and in accordance with predefined capacity and time frame.
Studies involve PK studies, mass balance and metabolism studies, QWBA and some other specialty studies, if necessary according to GLP standards
Compliance with German law, GLP, GCP, guidelines and other applicable regulation (e.g., radio protection) pertaining to the R&D process, study conduct, and registration of drugs
Responsible (and accountable as per delegation) for and enforce adherence to safety measures in laboratories
If you are looking for a challenge and opportunity to bring in your expertise and passion for DMPK into our high quality DMPK services and to impact our client drug development plans, this position might be of your interest
PhD in pharmaceutical sciences, analytical chemistry, veterinary medicine or pharmacist with 5 to 10 years of experiences in small molecule drug development in pharma industry or CRO
Strong knowledge and hands on experience with in-vivo non-clinical drug development
Experience with Phoenix WinNonLin
Experience with in-vitro drug metabolism is an asset
Experience in Laboratory Animal Science at FELASA C level is advantageous
Effective interpersonal and communication skills
Cooperative, self-motivated, with a can- do attitude
The ability to work to tight deadlines while maintaining high standards
Assume responsibility as deputy principal investigator according to German animal
welfare laws for all animal studies
A good understanding of working with radioactivity in support of mass balance and
metabolite identification studies
Experiences to work in a GLP accredited environment and adherences to corporate
and health authority quality standards and guidelines
Your excellent command of written and spoken English and German will enable you
to act in an international working environment

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