Clinical Lab Information Specialist
Precision for Medicine · Frederick, MD, USA
Posted about 3 months ago
or apply directly on Precision for Medicine's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 80 days Precision for Medicine's roles stay open a median of 77 days
- Reposted
- No
- Salary listed
- No 0% of Precision for Medicine's roles list one
- Ghost-job risk at Precision for Medicine
- high 118 stale, 4 reposted of 122 open
- Hiring momentum
- 246 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-10-23
Measured from postings appearing on and disappearing from Precision for Medicine's own greenhouse board since 2026-08-03. Full hiring picture for Precision for Medicine.
About this role
The Clinical Lab Information Specialist is responsible for supporting laboratory technology initiatives, focusing on User Acceptance Testing (UAT), system validations, and regulatory compliance documentation. This role involves coordinating UAT activities, ensuring systems meet regulatory standards, and serving as a liaison between laboratory operations, IT, and external vendors. The position requires strong clinical laboratory knowledge and expertise in system implementation and validation methodologies.
- benefits
- 3/5
- freshness
- 1/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Precision for Medicine as an employer.
What you need
- Bachelor’s Degree or Master Degree in Clinical Laboratory Science, Life Sciences, Health Informatics, or related field
- 5-8 years of related experience in clinical laboratory operations, laboratory informatics, or business analysis
- Strong experience with laboratory systems (LIS, LIMS, middleware, instrument interfaces)
- Demonstrated expertise in UAT coordination and execution
- Hands-on experience with system validation in regulated environments (GxP, CLIA, CAP, FDA)
- Experience authoring validation and regulatory documentation
Nice to have
- Experience with specific LIS platforms (e.g., Epic Beaker, SCC Soft, Sunquest, Cerner Millennium)
- Familiarity with data standards (HL7, interfaces, instrument connectivity)
- Experience in audit/inspection readiness and regulatory submissions
- Knowledge of electronic document management systems (eDMS) and change control processes
What you get
- Discretionary annual bonus
- Health insurance
- Retirement savings benefits
- Life insurance and disability benefits
- Parental leave
- Paid time off for sick leave and vacation
Worth weighing
- Position is fully onsite in Frederick, MD
- No specific salary mentioned, but a range of $83,200 — $124,800 USD is provided
- Compensation decisions depend on various factors and may not be at the top of the range
- Candidates must be legally authorized to work in the country without employer sponsorship
Summarised from Precision for Medicine's posting. Read the full original.
Listed by Precision for Medicine on their greenhouse job board, last confirmed open on 2026-10-23. PitchMeAI is not the employer.
More roles at Precision for Medicine
- Clinical Research Associate I/ Clinical Research Associate IIRemote, France
- Senior Project Manager - OncologyRemote, United States
- Senior Clinical Research Associate (Argentina)Remote, Argentina
- Clinical Project Manager / Senior Clinical Project ManagerRemote, Slovakia
- Clinical Trial ManagerRemote, China
- Clinical Project Manager / Senior Clinical Project ManagerRemote, Spain
- Clinical Project Manager / Senior Clinical Project ManagerRemote, Romania
- Senior Clinical Research Associate/ Clinical Research Associate IIRemote, United Kingdom