descripción del trabajo

MAIN DUTIES RESPONSIBILITIESManage bioanalytical method development projects, with focus on NCEs, peptides and oligonucleotides.Coordinate the validation of analytical methods to quantify drugs, metabolites or biomarkers in biological matrices by LC-MS/MS according to international guidelines.Coordinate sample analysis projects, including regulated and non-regulated, pre-clinical and clinical studies.Deliver extensive and effective communication with sponsors and timely delivery of results.Effectively resolve technical and regulatory issues.Organize and line-manage laboratory personnel.Actively support Senior Management and participate in strategic projects to optimize procedures.REQUIRED PROFILE QUALIFICATIONSMinimum 5-years experience in bioanalytical CROs.PhD, MSc or BSc in chemistry or related subject.Experience working with NCEs. Also, experience with peptides and oligonucleotides will be highly valued.Proven, extensive knowledge of HPLC, UHPLC and mass spectrometry.Deep understanding of international bioanalytical guidelines, and experience working under GLP/GCP regulations.Excellent level of English (Spanish – nice to have).Experience working with LIMS systems.OTHER REQUIRED SKILLSStrong communication and organization skills, and capacity to work in teams.Proactive and hands-on approach.High level of motivation and enthusiastic personality.WHAT IS OFFEREDOpportunity to work and contribute to the success of an expanding CRO.Solid scientific team with career growth opportunities.Cutting edge laboratory with the latest technology.International and multicultural environment in company based in Barcelona.Diligent, professional organization, with a human touch. #J-18808-Ljbffr