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Remote Clinical Genomics Jobs in Spring, TX (NOW HIRING)

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How much do remote clinical genomics jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for remote clinical genomics in Spring, TX is $30.80, according to ZipRecruiter salary data. Most workers in this role earn between $14.76 and $29.33 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote Clinical Genomics Specialist, and why are they important?

To thrive as a Remote Clinical Genomics Specialist, you need a strong background in genetics, molecular biology, and clinical data interpretation, typically supported by a degree in genetics or a related field. Familiarity with bioinformatics software, genomic databases, and tools like Next-Generation Sequencing (NGS) analysis platforms is essential, and certifications such as CGC (Certified Genetic Counselor) may be preferred. Excellent communication, attention to detail, and problem-solving skills help in explaining complex genomic information to both clinicians and patients remotely. These skills are crucial for delivering accurate, actionable genomic insights that improve patient care and support collaborative diagnostic decision-making.

How do remote clinical genomics professionals typically collaborate with laboratory teams and healthcare providers?

Remote clinical genomics professionals often work closely with laboratory staff, genetic counselors, and physicians through digital communication platforms, such as secure email, video conferencing, and specialized lab management software. They may be responsible for interpreting genetic test results, preparing reports, and discussing findings in virtual team meetings. This collaborative approach ensures that patient care remains seamless, even when team members are geographically dispersed. Strong communication skills and familiarity with digital collaboration tools are essential for success in this role.

What is a Remote Clinical Genomics professional?

A Remote Clinical Genomics professional is a specialist who analyzes genetic data and interprets genomic information to assist in diagnosing and treating patients—all while working remotely. They may work with physicians, researchers, and laboratories to provide insights into genetic disorders and recommend personalized treatment plans. Their work often involves using advanced bioinformatics tools and communicating findings to healthcare teams, patients, or research groups. Remote roles in this field require strong analytical skills, attention to detail, and knowledge of genetics and clinical workflows.
What are popular job titles related to Remote Clinical Genomics jobs in Spring, TX? For Remote Clinical Genomics jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Genomics jobs in Spring, TX look for? The top searched job categories for Remote Clinical Genomics jobs in Spring, TX are:
What cities near Spring, TX are hiring for Remote Clinical Genomics jobs? Cities near Spring, TX with the most Remote Clinical Genomics job openings:
Remote Clinical Genomics jobs near you
Associate Director, Assay Validation

Associate Director, Assay Validation

Baylor Miraca Genetics Laboratories

Houston, TX • On-site, Remote

Full-time

Posted 5 days ago

Job description

KEY RESPONSIBILITIES

  • Lead the planning, design, and execution of analytical validation studies for sequencing-based assays, including germline, somatic, and liquid biopsy applications.
  • Develop and maintain validation strategies, protocols, and reports that comply with CLIA, CAP, NYS, and internal quality standards.
  • Collaborate with Assay Development, Bioinformatics, Quality, and Product teams to align validation strategy with assay design, clinical claims, and product readiness.
  • Establish acceptance criteria, reference materials, and performance metrics to support analytical and clinical validation activities.
  • Serve as the subject matter expert for NGS validation methods, study design, assay performance characterization, and regulatory expectations.
  • Analyze validation data and provide data-driven recommendations for assay optimization, issue resolution, and launch readiness.
  • Support regulatory or laboratory inspections and contribute to responses, documentation, or corrective action plans as needed.
  • Mentor scientists at different levels and contribute to building a scalable validation function within the R&D organization.
  • Maintain up-to-date knowledge of emerging trends, technologies, and regulatory guidance in NGS assay validation and clinical genomics.
  • Perform other duties as assigned to support team and organizational objectives.
  • Comply with all company policies, procedures, and applicable regulatory requirements.

QUALIFICATIONS

Required

  • PhD. in Molecular Biology, Genetics, Genomics, or a related discipline with 6+ years of relevant experience; or M.S. with 8+ years of experience in NGS assay development and validation.
  • Demonstrated track record leading validation of clinical NGS assays under CLIA, CAP, NYS, or equivalent regulatory frameworks.
  • Strong expertise in NGS library preparation, sequencing platforms, and assay performance characterization.
  • Deep understanding of analytical validation parameters, including accuracy, precision, limit of detection, specificity, reproducibility, and related statistical evaluation.
  • Experience collaborating with bioinformatics teams for pipeline verification and integrated assay validation.
  • Familiarity with quality management systems, design control, and documentation best practices.
  • Excellent problem-solving, communication, and cross-functional collaboration skills.
  • Proven ability to lead complex projects and influence without direct authority in a matrixed environment.
  • Equivalent combination of education and experience may be considered.

Preferred:

  • Prior experience with germline clinical genetic testing or prenatal liquid biopsy testing.
  • Knowledge of NYS clinical test submission requirements or FDA IVD development processes.
  • Experience managing a small team.
  • Familiarity with automation or process scaling for NGS workflows.

COMPETENCIES

  • Scientific rigor and strong attention to detail.
  • Strategic thinking with hands-on execution capability.
  • Collaborative mindset with strong communication across scientific and business functions.
  • Commitment to quality, compliance, and continuous improvement.

PHYSICAL DEMANDS AND WORK ENVIRONMENT

  • Location: Houston, TX / Remote.
  • Work may be performed in an office, remote, and/or laboratory environment depending on business needs and assigned responsibilities.
  • May require exposure to standard laboratory conditions and adherence to applicable safety, quality, and regulatory requirements.
  • Must be able to use standard office equipment and computer systems for extended periods.
  • Travel requirements may vary based on business needs.

EEO STATEMENT

Baylor Genetics is proud to be an equal opportunity employer committed to fostering an inclusive and diverse workplace. We welcome and encourage applicants from all backgrounds to apply. We do not discriminate on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, pregnancy, childbirth, or any other status protected by applicable federal, state, or local law.

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