Entry-Level Bioanalytical Scientist, Pharmacokinetics, Onsite

The Associate Scientist (R1) is an entry-level scientific position responsible for supporting the development, qualification, validation, and application of bioanalytical methods used to quantify drug candidates, and metabolites in biological matrices. The successful candidate will perform laboratory experiments, analyze data, document results, and contribute to the delivery of high-quality bioanalytical data supporting preclinical and clinical drug development programs. This role provides an opportunity to develop technical expertise in regulated bioanalysis while working within a collaborative, multidisciplinary environment operating under Good Laboratory Practice (GLP) and GxP standards.

Conduct routine laboratory experiments supporting bioanalytical method development, qualification, validation, and sample analysis. Perform sample preparation, data acquisition, data review, and interpretation using established analytical platforms. Maintain accurate laboratory records, electronic notebooks, and study documentation in compliance with regulatory requirements. Assist in the preparation of study protocols, validation reports, study reports, and other regulatory documentation. Participate in troubleshooting analytical methods, instrumentation, and laboratory processes. Collaborate with scientists, project teams, quality organizations, and program stakeholders to ensure timely delivery of scientific data. Follow all company safety, environmental, and quality requirements. Contribute to laboratory operational excellence initiatives, including automation, process improvements, and continuous improvement projects. Communicate scientific findings effectively through presentations, technical summaries, and team discussions.

Bachelor's Degree in Biology, Biochemistry, Chemistry, Pharmaceutical Sciences, Immunology, Molecular Biology, or another related scientific discipline Demonstrated laboratory experience through academic research, internships, co-op placements, or industry experience. Strong analytical and problem-solving skills. Ability to carefully follow experimental procedures and document work accurately. Effective written and verbal communication skills. Strong organizational skills and attention to detail. Ability to work both independently and collaboratively within a team environment.

Experience with regulated bioanalysis, GLP, Good Manufacturing Processes (GMP), or GxP environments. Hands-on experience with ligand binding assays, cell-based assays, Liquid Chromatography- Mass Spectrometry (LC-MS/MS), or automated laboratory platforms. Familiarity with biological sample handling and immunogenicity testing. Knowledge of (Food Drug Administration) FDA, (European Medical Agency) EMA, and (Internation Council for Haromisation) ICH bioanalytical method validation guidance. Experience with scientific data analysis and reporting software Key Success Factors Demonstrates a strong learning mindset and willingness to develop scientific expertise. Embraces feedback and continuously improves technical and professional skills. Maintains a high standard of scientific integrity and data quality. Prioritizes safety, compliance, and teamwork. Shows adaptability and curiosity in addressing scientific and operational challenges. clinicaltrialjobs eligibleforERP Required Skills: Adaptability, Clinical Research, Communication, Compliance Frameworks, Compliance Reporting, Data Analysis, Data Governance, Data Reporting, Project Coordination, Records Management, Stakeholder Relationship Management, Teamwork Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal