Clinical Pharmacology System Analyst

Cambridge, Cambridge, Massachusetts, United States

7 - 10 Years

Consultant

Job Description
:
Clinical Pharmacology Systems Specialist

Location
: USA (Hybrid, in office when needed)

Working hour
s: US Eastern Time (EST)

Experience
: 8+ years

Department :
Clinical Pharmacology, working closely with IT, QA, Info Sec, Data Security and AI teams

We need an experienced Clinical Pharmacology Systems Specialist to connect our Clinical Pharmacology (Clin Pharm) team with IT. You'll handle the technical side of Clin Pharm tools and platforms: setting them up, deploying them and keeping them running. You'll also make sure every system follows GxP rules and is fully validated and documented. You'll also help us bring AI and LLM (large language model) tools into Clin Pharm work in a safe and compliant way.

• IT Liaison and Communication
• Be the main link between the Clinical Pharmacology team and IT for anything technical.
• Lead communication with IT whenever Clin Pharm tools are set up, upgraded or maintained.
• Turn Clin Pharm business needs into clear technical requirements, and explain technical limits back to scientists in simple terms.
• Track open requests, issues and timelines, and keep everyone informed.
• Tool and Platform Implementation
• Help deploy, implement, and maintain Clin Pharm platforms and tools (for example PK/PD modeling software, NCA tools, data platforms and scientific computing environments).
• Take part in the full system lifecycle: requirements, vendor review, installation, setup, testing, go-live and support
• Plan and support upgrades, patches, change requests and system retirement.
• Make sure systems stay available and reliable, and handle incidents with IT.

• Plan and run GxP testing, including IQ, OQ and PQ, user acceptance testing (UAT) and regression testing.
• Write and maintain validation documents, such as validation plans, user and functional requirements, risk assessments, test scripts, traceability matrices, summary reports and SOPs.
• Build and improve GxP processes around each tool, covering change control, access management, audit trails, backup and restore, and periodic review.
• Follow 21 CFR Part 11, EU Annex 11, GAMP 5 and data integrity (ALCOA+) principles.
• Support internal audits and regulatory inspections that involve Clin Pharm systems.

• Keep up with AI and LLM tools that could help clinical pharmacology work.
• Help evaluate, deploy and implement AI/LLM solutions with the AI, IT and Info Sec teams.
• Help set up validation, governance and risk controls for AI tools used in a GxP setting.
• Work closely with IT, QA, Info Sec, Data Security and AI teams.
• Make sure new tools pass security reviews, data privacy checks and QA approval before go-live.
• Coordinate with outside vendors on implementation, support and validation packages.

• Bachelor's or Master's degree in Life Sciences, Pharmacy, Computer Science, Information Systems or a related field
• 8+ years of experience in pharma, biotech or a CRO, in a role covering IT systems, computer system validation (CSV/CSA) or scientific platform support.
• Hands-on experience with GxP testing and validation documentation.
• Proven experience deploying and maintaining enterprise or scientific software.
• Good knowledge of 21 CFR Part 11, EU Annex 11, GAMP 5 and data integrity rules.
• Working knowledge of AI and LLM tools, including how they are deployed and the risks and controls they need.
• Strong communication skills, with the ability to explain technical topics to non-technical people and the other way round.
• Available during US EST hours and able to come into the office when needed.

• A background in clinical pharmacology, or knowledge or experience of it (PK/PD, NCA, population PK, exposure-response).
• Familiarity with Clin Pharm tools such as Phoenix Win Nonlin/NLME, NONMEM, R/RStudio, Monolix, Simcyp or similar.
• Experience with cloud platforms (AWS), Linux servers or high-performance computing environments
• Exposure to CSA (Computer Software Assurance) approaches.
• Project management or ITIL certification.

01-10-2026

JOB
880

Scientific Informatics

Location Cambridge, Cambridge, Massachusetts, United States