Clinical Biospecimen Operations Associate
Natera, Inc. - Austin, TX
Posted Jun 11, 2026
Benefits
- Parental leave
- Not verified
- Non-birth-parent leave
- Not verified
- Family-building benefits
-
- Fertility benefits: Not verified
- Adoption assistance: Not verified
- Surrogacy assistance: Not verified
- Mental health support
- Not verified
- Relocation assistance
- Not verified
- Childcare support
- Not verified
- Learning budget
- Not verified
- Verification
- Not verified
- Salary
- $88K-$110K not verified - source not recorded; timestamp not recorded
- 401(k) match
- Not verified
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Market context
- U.S. role benchmark (BLS OEWS)
- $81,444 U.S. median for this role
- Projected growth (BLS Employment Projections)
- +6.9% - Faster than average
22% above the BLS role benchmark for healthcare aggregate.
Matched to SOC 29-1141 - Healthcare aggregate by role bucket.
Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.
Schedule
- Shift type
- Not verified
- Weekend work
- Not verified
Application
- Cover letter
- Not verified
- Assessment
- Not verified
- Deadline
- Not stated
Where they hire
State eligibility is not yet verified.
About this role
Clinical Biospecimen Operations Associate Austin, TX POSITION SUMMARY: The Clinical Biospecimen Operations Associate executes oncology clinical research studies, including coordination of all operational activities required for tracking, testing and reporting clinical trial samples. This position will perform required job duties with oversight from the Pharma Operations Team Leader and will work closely with internal and external central testing laboratories, vendors, Data Management, Product Management, Engineering and external collaborators in compliance with the study protocol(s), SOPs, and applicable regulatory requirements. PRIMARY RESPONSIBILITIES: - Maintain oversight of all study sample operational activities including planning, coordinating and tracking clinical trial sample testing to ensure results are provided within agreed upon TAT - Work with Data Management to develop and maintain dashboards and KPIs representing metrics and trends related clinical trial sample testing and the status of clinical studies and present to study teams and management teams, as needed. - Meticulously track clinical trial samples from sample receipt to result reporting to investigator sites and/or external collaborators (and sample return, if applicable) - Utilize operational and project management skills to anticipate, investigate and resolve issues to ensure deliverables and TAT are met; raise issues to Pharma Operations Team Leader - Responsible for handling data files to support timely result reporting - Review and provide input to clinical study protocol for sample collection requirements and alignment with the SOW, study plans and company policies - Administer clinical trial supplies related to biospecimen collection, processing, shipment, and storage as, well as maintenance of associated tracking information
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