Chief Scientific Officer (CSO) – Clinical Diagnostics & Assay Development
Job Title: Chief Scientific Officer (CSO) – Clinical Diagnostics & Assay Development
Job Type: Full-Time | On-Site
Position Overview
We are seeking an experienced and visionary Chief Scientific Officer (CSO) to lead scientific strategy, technical operations, and laboratory leadership within a clinical diagnostics and research environment. The ideal candidate will oversee research, assay development, laboratory operations, regulatory compliance, and scientific innovation while managing a multidisciplinary scientific team.
Key Responsibilities
Scientific Leadership
- Develop and execute the organization's long-term
scientific strategy
- Identify emerging trends and opportunities in molecular diagnostics, genetics, and
laboratory medicine
Assay Development & Validation
- Lead the design, development, optimization, and validation of
Laboratory Developed Tests (LDTs)
- Oversee analytical and clinical validation studies for high-complexity testing
Laboratory Operations
- Direct and supervise
high-complexity clinical laboratory operations
- Manage laboratory personnel, workflows, and technical performance
Regulatory Compliance
-
Ensure compliance with CLIA, state regulations, accreditation standards, and other applicable laboratory requirements
-
Support laboratory inspections, audits, and quality management activities
Cross-Functional Collaboration
- Collaborate with executive leadership and clinical teams to align scientific capabilities with business and clinical objectives
Scientific Representation
- Represent the organization at scientific meetings, conferences, and
industry events
Required Qualifications
Education
- Ph.D. in Molecular Biology, Genetics, Biochemistry, or a related life sciences field (required)
Experience
-
Minimum 2+ years of experience working in a clinical laboratory environment (required)
-
Minimum 2+ years of experience directing or supervising a high-complexity testing laboratory (required)
-
Experience with laboratory regulatory compliance and quality systems (required)
Technical Skills
- Strong expertise in molecular diagnostics and
assay development
- Experience with ELISA, enzyme chemistry, PCR, digital PCR, microarray technologies, and
multiplex testing platforms
- Knowledge of Laboratory Developed Tests (LDTs) and
clinical validation processes
Preferred Qualifications
-
Board certification such as ABMGG, ABB, or equivalent
-
Experience serving as or qualifying for a
High-Complexity Laboratory Director
Core Competencies
-
Leadership and team development
-
Strategic thinking and innovation
-
Problem-solving and analytical skills
-
Strong communication and presentation abilities
-
Attention to detail and regulatory compliance
Benefits
-
Health Insurance
-
Dental Insurance
-
Vision Insurance
-
Life Insurance
-
Paid Time Off (PTO)
Work Environment
-
Setting: Clinical Diagnostics and Research Environment
-
Culture: Scientific excellence, innovation, continuous improvement
-
Focus: Molecular diagnostics, assay development, high-complexity laboratory operations
-
Schedule: Full-Time, on-site with leadership responsibilities
Equal Opportunity Statement
All qualified applicants will receive consideration for employment without discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or any other protected status.
Ready to Lead Our Scientific Strategy?
If you are a visionary Chief Scientific Officer (CSO) with a Ph.D. or MD in Pathology, experience in high-complexity clinical laboratory leadership, and expertise in assay development and molecular diagnostics – apply today.
**[**Point of Contact
Jane Roy
Business Development Manager
P: 409-230-8844
E: jane.roy@firman-solutions.com
A: 2766 Duniven Cir Suite 206 Amarillo TX 79109**]**
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