Part-time Clinical Laboratory Scientist

RDI - Your IVD CRO; Los Angeles (CA); On-site; Part time

Job summary

An innovative company specializing in laboratory testing seeks a part-time Clinical Laboratory Scientist. This role involves leading clinical trial protocols, managing validation projects, and ensuring adherence to quality standards. Ideal candidates will have a strong background in the In Vitro Diagnostics field, excellent analytical and communication skills, and a passion for advancing diagnostic tools. Join a dedicated team committed to improving healthcare diagnostics, with opportunities for professional growth and development. If you're ready to make a significant impact in a dynamic environment, this position is perfect for you.

Qualifications

• Bachelor's degree in a relevant field required.
• Experience in In Vitro Diagnostics medical field preferred.

Responsibilities

• Coordinate and perform validation projects for equipment and methods.
• Manage lab inventory and document assay development.

Skills

Analytical Skills

Technical Expertise in Process Validation

Communication Skills

Problem-Solving

Leadership Ability

Education

Bachelor's in Biology

Bachelor's in Chemistry

Bachelor's in Life Science

Tools

Microsoft Office

Job description

Join to apply for the Part-time Clinical Laboratory Scientist role at RDI - Your IVD CRO

Get AI-powered advice on this job and more exclusive features.

About RDI
RDI is a project-based laboratory specializing in collecting and testing patient samples to evaluate lab instruments not yet available on the market. Founded in 2008, we've managed over 150 clinical trials and tested thousands of samples. Our mission is to contribute to better diagnostic tools, especially highlighted during the COVID-19 crisis.

Position Summary

The Clinical Research Laboratory Scientist will lead clinical trial protocols for method comparison and validation of Immunodiagnostic Assays, overseeing daily operations. This full-time, permanent position offers benefits, an aggressive salary, and significant leadership opportunities, ideal for career advancement. Preferred candidates have experience with Siemens, Roche, Abbott, Biorad, and Beckman instruments, and familiarity with Clinical Testing Protocols and IRB processes.

Responsibilities

• Coordinate and perform validation projects for equipment, methods, and processes.
• Conduct validation tests for new assays, instruments, and methodologies.
• Generate performance qualification, method comparison, and validation reports with the Chief Science Officer.
• Manage lab inventory for projects.
• Document assay development in scientific notebooks.
• Troubleshoot instruments and procedures, and write protocols and reports.
• Communicate with clients and coordinate testing activities.
• Travel for manufacturer training and industry conferences.
• Design and execute validation strategies adhering to quality standards.
• Maintain knowledge of relevant Medical Device regulations.
• Perform root cause analysis and suggest solutions for complex issues.
• Uphold high standards of quality, integrity, and cross-functional collaboration.
• Work safely and ethically in all duties.

Minimum Requirements

• Bachelor's in Biology, Chemistry, or related Life Science field.
• Experience in the In Vitro Diagnostics medical field.
• Strong analytical skills, including statistical methods/DOE.
• Technical expertise in process validation.
• Excellent communication skills.
• Problem-solving experience.
• Proficiency in Microsoft Office, especially Excel.
• Ability to work independently.
• Quick learner of new products and technologies.
• Hands-on microbiological lab skills.
• Leadership ability for project management.

Preferred Qualifications

• Experience in microbiological assay development, protein purification, PCR.
• Strong organizational skills.

Salary: $1 - $9,999,999,999 per year

Job posted by ApplicantPro