Job Description
Company Description
Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies.
With over 30 years of GLP compliance and certification, Eurofins Advinus serves diverse industries such as Biotech, Pharmaceutical, Biological, Agrochemical, Nutraceutical and Cosmetic. Eurofins Advinus is the only contract research organization (CRO) in India to have developed data in support of 90+ end-to-end IND enabling packages to be submitted to global regulators such as USFDA, EMA, MHRA, Health Canada and others.
Job Description
- Lead the assigned projects as study director/principal investigator and collaborate with various teams in executing the project.
- Planning and conduct of in vitro ADME studies such as metabolism, drug-drug interactions, and Caco-2 permeability
- Recording of raw data, data acquisition, compilation, analysis, and interpretation. Ensure data integrity and reporting with good accuracy
- Maintain the laboratory and equipment to minimize down time
- Communicate effectively and professionally with Sponsors, peers, team members, and other stakeholders
- Perform assigned work independently with minimum supervision and work as a team
Additional Information
- Ph.D with experience of 3-5 years or masters in Pharmacy/ biotech/ chemistry/ biochemistry or relevant field with experience of 5-8 years
- Demonstrated ability to train and supervise staff
- Sound knowledge of preclinical research and development
- Experience in LC-MS/MS based analysis, sample processing and handling of LC-MS/MS instrument
- Experience of conducting in vitro ADME studies including Caco-2 permeability assays