Scientist I/II - LC-MS/MS Bioanalysis

About the role

As a Scientist I/II - LC-MS/MS Bioanalysis, you will develop, optimize, troubleshoot, and validate bioanalytical methods supporting DMPK and regulated studies. You'll work with advanced LC-MS/MS and high-resolution mass spectrometry platforms while gaining exposure to a broad range of therapeutic modalities-from traditional small molecules to peptides, oligonucleotides, PROTACs, biologics, and emerging therapies. This opportunity is ideal for an early-career bioanalytical scientist who wants to expand beyond routine sample analysis and develop deeper expertise in method development, complex bioanalysis, scientific problem-solving, and study execution within a global CRO/CDMO environment.

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Responsibilities

• Develop, optimize, troubleshoot, and validate LC-MS/MS bioanalytical methods supporting drug discovery and development programs.
• Perform bioanalytical sample analysis for DMPK, method development, validation, and regulated studies.
• Operate LC-MS/MS and HPLC platforms and gain exposure to advanced mass spectrometry technologies.
• Design and execute scientifically sound experiments aligned with client objectives, study requirements, and internal quality standards.
• Process, analyze, interpret, and report bioanalytical data while identifying and resolving technical challenges.
• Review and execute study protocols and ensure accurate documentation of experimental procedures, results, and conclusions.
• Author and contribute to protocols, validation reports, technical summaries, study reports, and other scientific documentation.
• Support GLP and regulated bioanalytical activities in accordance with applicable procedures and quality requirements.
• Collaborate with scientists, project teams, management, Business Development, and clients to support successful project execution.
• Participate in scientific project reviews, technical discussions, and continuous improvement initiatives.