Research Associate II

Research Associate II

San Francisco, California, US

Contract | M-F 8-5

A clinical-stage biopharmaceutical company focused on developing innovative oncology therapeutics is seeking a talented Research Associate II to join their Pharmaceutical Sciences team. Our pipeline includes novel small molecule inhibitors targeting specific resistance mechanisms in genetically defined cancers.

• Perform sample analysis using standard laboratory techniques including weighing, pipetting, and operation of analytical instruments (HPLC, LC-MS, GC, UV-Vis, Karl Fischer, dissolution apparatus, etc.).
• Execute analyses with thorough understanding of test procedures, scientific principles, and proper instrument operation to ensure accurate and reliable results.
• Operate instrument control software for data collection, processing, calculation, and report generation.
• Maintain detailed and compliant laboratory notebook records ensuring traceability and consistency in documentation.
• Prepare test solutions, reagents, and samples following written protocols with precision.
• Develop presentation materials and communicate research findings to management and at team meetings.
• Collaborate cross-functionally with Process Chemistry and Formulation Development teams.

• B.Sc. in Chemistry with minimum 3 years of relevant research experience, OR M.Sc. in Chemistry with at least 1 year of pharmaceutical/biotech industry experience.
• Hands-on proficiency with analytical techniques including chromatography (HPLC, GC, LC/MS), spectroscopy (UV-Vis, FTIR), titration methods (Karl Fischer, acid-base), dissolution testing, particle size analysis (laser diffraction), microscopy and compendial methods.
• Experience with laboratory software systems (e.g., Chemstation, Empower, Excel) for data collection, analysis, and reporting.
• Strong initiative with proven problem-solving abilities and experimental design input.
• Track record of laboratory achievement and innovation.
• Knowledge of ICH guidelines, USP requirements, FDA guidance, and GLP practices.
• Exceptional organizational skills, attention to detail, and safety-consciousness.
• Ability to work independently and collaboratively in a fast-paced, multidisciplinary environment.

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.