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Precision Medicine Group

Clinical Lab Information Specialist

Precision Medicine Group · Frederick, MD, USA

Posted about 3 months ago

or apply directly on Precision Medicine Group's site. We never take the application ourselves.

Is this posting real?

This role has been open
80 days
Precision Medicine Group's roles stay open a median of 81 days
Reposted
No
Salary listed
No
0% of Precision Medicine Group's roles list one
Ghost-job risk at Precision Medicine Group
high
152 stale, 8 reposted of 157 open
Hiring momentum
309 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 Medicine Group's own greenhouse board since 2026-08-03. Full hiring picture for Precision Medicine Group.

About this role

The Clinical Lab Information Specialist is responsible for leading User Acceptance Testing (UAT) and ensuring system validations and regulatory compliance within laboratory technology initiatives. This role involves collaborating with laboratory operations, IT, and vendors to implement and maintain laboratory systems, while also developing necessary documentation and supporting audit activities. The position requires a strong understanding of clinical laboratory operations and regulatory standards.

Our read on this posting2.6out of 5
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 Medicine Group 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 listed, but a range is provided
  • Role requires strong regulatory compliance knowledge and experience in a highly controlled environment

Summarised from Precision Medicine Group's posting. Read the full original.

Listed by Precision Medicine Group on their greenhouse job board, last confirmed open on 2026-10-23. PitchMeAI is not the employer.

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