Clinical Laboratory Scientist-Senior Andrologist

IVI RMA GLOBAL; San Francisco (CA); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Comprehensive benefits package

Retirement plans

Paid time off

Limited overnight coverage

Job summary

IVI RMA GLOBAL is seeking a full-time Clinical Laboratory Scientist (CLS) – Senior Andrologist in San Francisco, California. This role involves performing and overseeing advanced andrology lab procedures, ensuring compliance with regulations, and supporting treatment.

Join a specialized fertility team that emphasizes collaboration and predictability. Enjoy a comprehensive benefits package while making a meaningful impact on patients' lives through reproductive medicine.

Qualifications

• Minimum five years of laboratory experience in andrology or reproductive medicine.
• Experience performing semen analysis and sperm preparation for ART procedures.
• Active California Clinical Laboratory Scientist (CLS) License.

Responsibilities

• Perform advanced diagnostic testing and maintain regulatory compliance.
• Supervise laboratory personnel and ensure quality standards.
• Support fertility treatment through andrology and hormone testing services.

Skills

Knowledge of male fertility diagnostics

Experience with SEMEN ANALYSIS

Leadership

Communication skills

Analytical skills

Education

Bachelor's Degree in Clinical Laboratory Science or related field

Master's Degree in a related scientific discipline

Tools

Roche Cobas e411

Laboratory Information Systems (LIS)

Electronic Medical Records (EMR)

Job description

Clinical Laboratory Scientist (CLS) – Senior Andrologist

IVI RMA North America is seeking a full‑time Clinical Laboratory Scientist (CLS) – Senior Andrologist to join our growing Andrology Department located in San Francisco, California. The Clinical Laboratory Scientist (CLS) – Senior Andrologist is responsible for performing and overseeing advanced andrology and reproductive laboratory procedures within a fertility clinic setting. This role supports male fertility evaluation, endocrine testing, and assisted reproductive technologies (ART) by performing semen analyses, sperm preparation, hormone testing, and laboratory quality management while ensuring compliance with California laboratory regulations.

Why Join IVIRMA?

Join a highly specialized fertility team where your expertise directly impacts patients on their family‑building journey. Unlike traditional hospital laboratory settings, this role offers a more predictable schedule, limited overnight coverage, and a supportive, collaborative environment focused on reproductive medicine.

What We Offer

• Predictable and stable scheduling
• Limited or no overnight coverage requirements
• Predictable weekend and holiday rotations
• Smaller team environment with greater visibility and collaboration
• Specialized reproductive medicine and fertility testing
• Opportunity to work alongside expert embryologists and fertility specialists
• Improved work‑life balance and reduced burnout compared to hospital laboratories
• Comprehensive benefits package, retirement plan, and generous paid time off

This is an excellent opportunity for an experienced Clinical Laboratory Scientist to grow their career with a global leader in reproductive medicine while making a meaningful difference in patients' lives.

Purpose

The Clinical Laboratory Scientist (CLS) – Senior Andrologist serves as the technical and operational leader for the Andrology and Endocrinology Laboratory. This position is responsible for performing advanced diagnostic testing, maintaining regulatory compliance, ensuring laboratory quality standards, supervising laboratory personnel, and supporting fertility treatment through andrology and hormone testing services.

All laboratory testing and procedures must be conducted in accordance with laboratory policies, CAP, CLIA, FDA, OSHA, HIPAA, and California Department of Public Health (CDPH) regulations. Attention to detail, technical expertise, leadership, and commitment to quality patient care are essential to success in this role.

Responsibilities

Andrology Laboratory Testing

• Perform diagnostic semen analysis according to WHO guidelines and laboratory protocols.
• Conduct advanced sperm function testing, including morphology assessment, motility and vitality analysis, sperm concentration and total motile count, DNA fragmentation testing when applicable.
• Prepare sperm samples for Assisted Reproductive Technologies (ART), including IUI, IVF, and ICSI.
• Process surgical sperm retrieval specimens, including TESA, PESA, and Micro-TESE.
• Review, validate, and accurately report andrology laboratory testing results.

Endocrinology & Hormone Testing

• Perform and oversee reproductive endocrinology testing related to fertility diagnostics.
• Operate immunoassay analyzers, including Roche Cobas e411, for hormone testing such as FSH, LH, Estradiol, Progesterone, AMH, Testosterone, hCG, Prolactin.
• Perform linearity verification and calibration verification (CALVER) according to laboratory validation protocols.
• Conduct and document CAP Proficiency Testing (PT) in compliance with CLIA and CDPH requirements.
• Troubleshoot analyzer performance issues and implement corrective actions as needed.
• Perform routine preventive maintenance, calibration checks, and functional verification of instrumentation.
• Monitor assay performance and maintain quality documentation for regulatory inspections.

Sperm Banking & Cryopreservation

• Perform sperm cryopreservation and thawing procedures for fertility preservation and donor banking.
• Maintain specimen tracking and chain‑of‑custody documentation.
• Ensure compliance with CAP, CLIA, FDA tissue regulations, and CDPH requirements.
• Monitor cryostorage systems and maintain accurate inventory records.

Laboratory Operations & Quality Management

• Maintain compliance with California Clinical Laboratory licensing regulations.
• Implement and maintain laboratory quality assurance and quality control programs.
• Perform method validation, verification studies, and instrument performance evaluations.
• Assist with preparation for CAP, CLIA, FDA, and CDPH laboratory inspections.
• Maintain laboratory documentation, standard operating procedures (SOPs), and quality records.
• Remain current on laboratory operating procedures, quality systems, regulatory standards, and industry best practices.
• Maintain compliance with OSHA safety requirements and infection control procedures.
• Support laboratory inventory management and cost‑control efforts while maintaining high‑quality laboratory services.

Leadership & Training

• Supervise, mentor, and train andrology laboratory personnel.
• Ensure staff competency assessments and continuing education compliance.
• Participate in hiring, onboarding, and performance management activities.
• Assist in the development, implementation, and revision of laboratory SOPs.
• Participate in internal audits, regulatory inspections, and laboratory readiness activities.
• Promote a culture of quality, collaboration, and continuous improvement.

Clinical Collaboration

• Work closely with reproductive endocrinologists, urologists, embryologists, and nursing staff.
• Provide technical consultation regarding male fertility testing, sperm preparation methods, and endocrine testing results.
• Participate in multidisciplinary patient case discussions and treatment planning.
• Collaborate with multidisciplinary teams to support excellent patient outcomes and achieve laboratory objectives.

General Responsibilities

• Maintain patient confidence and protect operations by keeping all patient and proprietary information confidential in accordance with HIPAA requirements.
• Adhere to all company policies and procedures.
• Perform other duties as assigned to support laboratory and patient care needs.

Academic Training

• Bachelor's Degree or higher in Clinical Laboratory Science, Biology, Biochemistry, Medical Technology, or a related scientific field – required
• Master's Degree in a related scientific discipline – preferred

Licensure

• Active California Clinical Laboratory Scientist (CLS) License issued by the California Department of Public Health (CDPH) – required

Requirements

• Minimum five (5) years of laboratory experience in fertility, andrology, reproductive medicine, or related clinical laboratory environments – required
• Experience performing semen analysis and sperm preparation for ART procedures – required
• Experience performing reproductive endocrinology testing and hormone immunoassay testing – required
• Experience operating and troubleshooting Roche Cobas e411 or similar immunoassay analyzers – required
• Ability to work in a high‑volume, fast‑paced laboratory environment.
• Ability to communicate clearly and effectively with patients, physicians, and team members.
• Ability to work weekends, early mornings, overtime, and on‑call schedules as needed.
• Ability to travel and provide support to satellite laboratory locations when required.
• Excellent organizational, analytical, interpersonal, leadership, and problem‑solving skills.

Preferred Qualifications

• Experience working in IVF or Assisted Reproductive Technology laboratories.
• Familiarity with CAP accreditation standards, CLIA requirements, FDA regulations, and CDPH laboratory regulations.
• Experience with instrument validation, proficiency testing programs, and laboratory inspections.
• Previous supervisory or team leadership experience within a clinical laboratory setting.

Technical Skills

• Electronic Medical Records (EMR) experience – required
• Laboratory Information System (LIS) experience preferred
• Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)
• Advanced knowledge of male fertility diagnostics and semen analysis methodologies
• Expertise in ART sperm preparation techniques
• Strong understanding of endocrinology testing and immunoassay instrumentation
• Ability to troubleshoot laboratory equipment and perform technical maintenance
• Thorough knowledge of CAP, CLIA, FDA, and CDPH regulatory compliance requirements
• Strong documentation and quality management skills

Physical Requirements

• Ability to sit at a microscope for extended periods while performing semen analyses and sperm preparation procedures.
• Some standing, stooping, bending, and reaching above shoulder level.
• Moderate lifting of up to 35 pounds.
• Manual dexterity and finger coordination required for pipetting and laboratory procedures.
• Ability to perform repetitive laboratory tasks with precision and accuracy.
• Visual acuity and eye‑hand coordination necessary for microscopic evaluations.
• Sensory requirements of speech, touch, vision, and hearing within normal range, with or without correction.
• Must be able to drive and travel between clinical sites as needed.

Environmental Conditions

• Work performed primarily in a temperature‑controlled fertility clinic laboratory environment.
• Frequent handling of human reproductive specimens and biological materials.
• Occupational exposure to bloodborne pathogens and potentially infectious materials.
• Exposure to laboratory reagents, liquid nitrogen, cryostorage systems, and electrical laboratory equipment.
• Potential physical hazards including burns, cuts, needle sticks, and equipment‑related injuries.
• May require early morning, weekend, holiday, or on‑call work depending on clinical schedules.
• Work routines and schedules may occasionally change with limited notice based on patient care needs.

Benefits

• Medical, Dental, Vision Insurance Options
• Retirement 401K Plan
• Paid Time Off & Paid Holidays
• Company Paid: Life Insurance & Long‑Term Disability & AD&D
• Flexible Spending Accounts
• Employee Assistance Program
• Tuition Reimbursement

About IVIRMA Global

IVIRMA is the largest group in the world devoted exclusively to human Assisted Reproduction Technology. Along with the great privilege of providing fertility care to our patients, IVIRMA embraces the great responsibility of advancing the field of human reproduction. IVIRMA Innovation, as one of the pillars of IVIRMA Global, is a renowned leader in fertility research and science. Check out our websites at: https://rmanetwork.com/ and https://www.ivirma.com/

EEO

IVIRMA is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: IVIRMA is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at IVIRMA are based on business needs, job requirements and individual qualifications, without regard to race, color, religion and/or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. IVIRMA will not tolerate discrimination or harassment based on any of these characteristics. IVIRMA encourages applicants of all ages.