This a great opportunity for a talented DMPK Principal Scientist to support the in vitro DMPK team.
The successful candidate will be accountable for developing, implementing, and validating analytical methods that support the company's drug development program. They will also have the responsibility for providing support for bioanalytical method development and validation in a fast-paced environment. In addition to these responsibilities, the successful candidate will collaborate with other scientists on projects related to drug metabolism, pharmacokinetics, and toxicology.
Our client is an award-winning provider of fully integrated drug discovery research programmes to the global pharmaceutical industry. Its mission is to help researchers develop new medicines by connecting them with the right collaborators and funding opportunities. Their team of experts works with scientists, clinicians, and businesspeople across all stages of drug development to ensure that their discoveries are turned into effective treatments as quickly as possible.
Responsibilities:
- To plan and execute in vitro drug metabolism and pharmacokinetic studies to understand the absorption, metabolism, distribution, and excretion (ADME) of drug candidates.
- Planning and performing in vitro DMPK studies to support drug development activities through the lifecycle of new chemical entities
- Conducting experimental design, data analysis and interpretation, and reporting of results using appropriate statistical methods
- Providing technical support to the in vitro DMPK team when needed
Qualifications:
- BSc., MSc. and/or PhD. in Pharmaceutical Sciences, Chemistry, Biochemistry, Biology, or a related discipline
- 10+ years' experience in performing in vitro DMPK assays
- Familiarity with quantitative LC-MS/MS techniques and basic troubleshooting
Benefits:
- Employee training and development
- Comprehensive benefits package, competitive salaries, and annual merit raises
- Bonus scheme, a well-regarded pension plan, and private medical insurance