Benefits:
401(k)
Bonus based on performance
Dental insurance
Health insurance
Wellness resources
Position Summary:
Crystal Bio Solutions is a GLP/GCLP-compliant CRO specializing in bioanalysis and biomarker services for pharma and biotech clients worldwide.
We are seeking a Director of LBA (Ligand Binding Assay) Platforms to lead scientific operations and people management across our LBA function. This role requires both deep technical expertise and strong leadership capability to manage scientists at multiple levels, maintain global client relationships, and drive project success in a regulated environment.
Key Responsibilities:
Lead a team of supervisors, Ph.D., and non-Ph.D. scientists to ensure the development, validation, and execution of LBA-based assays (PK, ADA, PD Biomarkers) in compliance with GLP/GCLP standards.
Directly manage supervisors and junior staff by setting clear expectations, supporting career development, and ensuring high performance.
Train and mentor team members as needed to build scientific strength, compliance awareness, and project ownership.
Serve as Principal Investigator (PI) on client studies, overseeing protocol development, study conduct, and reporting.
Communicate clearly with clients and manage expectations throughout all phases of assigned projects to ensure satisfaction and alignment.
Maintain strong relationships with global clients, supporting both ongoing and future project opportunities with responsiveness and trust.
Provide scientific and operational leadership as Subject Matter Expert (SME) in LBA technologies including ELISA and MSD (Meso Scale Discovery).
Review and approve study plans, validation protocols, reports, and key regulatory documentation.
Represent Crystal Bio Solutions at scientific conferences, industry networking events, and in client-facing presentations.
Support business development by providing technical insights for client proposals and quote generation.
Ensure efficient lab operations through SOP adherence, workflow improvements, and cross-functional collaboration (QA, BD, PM).
Foster a culture of excellence, accountability, and compliance.
Qualifications & Educational Requirements:
Ph.D. with 10+ years, Master’s with 15+ years, or Bachelor’s with 18+ years of relevant experience in Bioanalysis within Pharma, Biotech, or CRO settings.
At least 3–5 years of people management experience, including direct supervision of scientific staff.
Extensive background in GLP/GCLP-regulated bioanalytical method development and validation for PK, ADA, and Biomarker assays.
Strong client communication skills and the ability to manage global client accounts with professionalism and clarity.
Experience presenting at industry events or scientific meetings is preferred.
Familiarity with LIMS (Watson preferred) and bioanalytical compliance practices.
Must be quality-driven, client-focused, and capable of working in a fast-paced CRO environment.