Director of Ligand Binding Assays

A leading GLP/GCLP-compliant contract research organization (CRO) is seeking a Director of Ligand Binding Assay (LBA) Platforms to oversee scientific operations and team leadership within its bioanalysis and biomarker division. This role combines deep technical expertise with strong leadership to manage a multidisciplinary team, maintain client relationships, and ensure project success in a regulated environment.

Key Responsibilities

• Lead a team of supervisors and scientists (Ph.D. and non-Ph.D.) in the development, validation, and execution of LBA-based assays (PK, ADA, PD Biomarkers) under GLP/GCLP compliance.
• Provide direct supervision, mentorship, and performance management to scientific staff.
• Foster scientific growth, regulatory awareness, and project accountability across the team.
• Act as Principal Investigator (PI) on client studies, overseeing protocol development, execution, and reporting.
• Maintain clear and professional communication with clients throughout project lifecycles.
• Build and sustain strong relationships with global clients, supporting both current and future collaborations.
• Serve as a Subject Matter Expert (SME) in LBA technologies, including ELISA and Meso Scale Discovery (MSD).
• Review and approve study plans, validation protocols, reports, and regulatory documentation.
• Represent the organization at scientific conferences, industry events, and client meetings.
• Support business development by contributing technical insights to proposals and pricing.
• Ensure efficient lab operations through SOP adherence, workflow optimization, and cross-functional collaboration.
• Promote a culture of scientific excellence, compliance, and accountability.

Qualifications

• Ph.D. with 10+ years, Master's with 15+ years, or Bachelor's with 18+ years of relevant experience in bioanalysis within pharmaceutical, biotech, or CRO environments.
• Minimum of 3-5 years of experience managing scientific personnel.
• Proven expertise in GLP/GCLP-regulated method development and validation for PK, ADA, and biomarker assays.
• Strong communication skills and experience managing global client accounts.
• Experience presenting at scientific or industry events is a plus.
• Familiarity with LIMS systems (Watson preferred) and bioanalytical compliance standards.
• Must be quality-focused, client-oriented, and adaptable to a fast-paced CRO setting.