Lead Clinical Laboratory Scientist - Sacramento, CA

Work Schedule

Environmental Conditions

Job Description

Job Summary: We are seeking a highly skilled and experienced Lead Clinical Laboratory Scientist (CLS) to join our Molecular Oncology Lab. The Lead CLS will play a crucial role in overseeing the day-to-day operations of the lab, ensuring that all protocols are rigorously followed, and providing guidance and support to junior staff members. This position is crucial for maintaining the high standards of our clinical trials and ensuring accurate and reliable results.

• Protocol Adherence: Ensure that all laboratory protocols and standard operating procedures (SOPs) are followed meticulously.
• Bench Work: Actively participate in bench work, including the preparation, processing, and analysis of clinical trial samples.
• Quality Control: Coordinate quality control procedures to ensure the accuracy and reliability of test results.
• Training and Mentorship: Provide training, mentorship, and support to junior staff members, answering their questions and assisting with complex procedures.
• Troubleshooting: Identify and resolve technical issues that arise during laboratory procedures.
• Documentation: Maintain accurate and detailed records of all laboratory activities, including sample processing, test results, and quality control measures.
• Compliance: Ensure compliance with all regulatory requirements, including CLIA, CAP, and other relevant standards.
• Collaboration: Work closely with the Laboratory Director and other team members to ensure the smooth operation of the lab and the successful completion of clinical trials.
• Continuous Improvement: Engage in continuous improvement initiatives to improve laboratory efficiency and effectiveness.

• Education: Bachelors degree required in Clinical Laboratory Science, Molecular Biology, or a related field.
• Certification: Valid CLS license required
• 5 plus years of experience in a clinical laboratory setting
• 2 plus years in a molecular oncology lab preferred
• Experience in a clinical trial setting preferred
• Advanced certification in molecular diagnostics or oncology preferred

Skills:

1. Strong technical skills in molecular biology techniques, including PCR, qPCR, NGS, and other relevant methodologies.

2. Excellent problem-solving and troubleshooting abilities.

3. Strong leadership and mentorship skills.

4. Attention to detail and a dedication to maintaining high standards of quality.

5. Strong ability to collaborate effectively with team members and other departments.

• The position requires working in a laboratory environment with exposure to biological samples and hazardous materials.
• Must have availability to work occasional weekends and holidays to meet the needs of clinical trials.

Compensation and Benefits

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

• A choice of national medical and dental plans, and a national vision plan, including health incentive programs

• Employee assistance and family support programs, including commuter benefits and tuition reimbursement

• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

• Employees Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: