Associate Research Scientist

Job description

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as an Associate Research Scientist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. Purpose Performs complex laboratory analysis and method R&D of pharmaceutical products and proficiently uses LC-MS/MS systems, analyzes samples, calculates and analyzes data and records data in adherence with SOP's and the industry. Major Job Responsibilities • Independently performs method validations, method transfers and analytical testing of pharmaceutical and biopharmaceutical compounds with LC-MS/MS systems. Understands and conforms to methods and protocols applicable to assigned tasks. Designs and executes experiments with minimal supervision. • Prepares study protocols, project status reports, final study reports and other project-related technical documents. • Reviews, interprets and analyzes data for technical, quality and compliance to protocols, methods and SOPs. • Communicates data and technical issues to the client and responds to client needs and questions. • Mentors, trains and coordinates laboratory activities of other team members and assists in troubleshooting instrument and analytical problems. • Assists with quality systems and new equipment. • Deep insight in method development. Education/Experience • Bachelor's degree in Chemistry or related field with over 5 years of experience in an analytical testing laboratory with LC-MS/MS. Pre-clinical GLP TK or clinical PK bioanalysis with LC-MS/MS in CRO experience is preferred. • LC-MS/MS bioanalysis method development experience in GLP or Non-GLP environment for pre-clinical or clinical studies is preferred. Knowledge, Skills and Abilities Required • Solid understanding and knowledge of general chemistry and separation science. • Full understanding of laboratory requirements LC-MS/MS systems, SOPs, ICH guidelines, EMA requirements and FDA guidance. • Ability to utilize Microsoft Excel and Word to perform tasks • Proven problem solving and troubleshooting abilities • Effective oral and written English communication skills • Time management and project management skills • Ability to work in a collaborative work environment with a team