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# SKDL Programming Lead - FSP - Remote (UK or Ireland)

- **Company:** PAREXEL
- **Location:** UK (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Microsoft Excel, Application Programming Interfaces (APIs), Clinical Data Repository, Computer Programming, Databases, Programming Tools, Perl (Programming Language), R (Programming Language), Python (Programming Language), Laboratory Information Management Systems, Microsoft Office, SQL Databases, Data Management, Programming Languages
- **Published:** October 22, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=21d44b74a8e982f8

## About the Role

* Strong project management, organizational, and analytical problem-solving capabilities within a matrix environment.
 * Experience working in clinical research, biotechnology, pharmaceutical, academic, or Contract Research Organization environments.
 * The ability to build productive partnerships across multidisciplinary teams and communicate effectively with internal and external stakeholders.
 * A quality-focused approach with strong attention to detail and commitment to advancing clinical research outcomes.
 * Comfort working with laboratory databases, biomarker data, sample management processes, and role-specific technology platforms., * Bachelor's degree in Life Sciences or equivalent discipline such as Science, Technology, Engineering, or Mathematics, or relevant work experience. Biology or a related major preferred.
 * Minimum of 6 years of clinical research experience within an academic institution, Contract Research Organization, pharmaceutical company, or biotechnology organization.
 * Working knowledge of clinical drug development, clinical databases, ICH-GCP guidelines, and applicable regulatory requirements including FDA and local country regulations as appropriate.
 * Proficiency with Microsoft Office applications, including strong Excel capabilities, and relevant role-specific systems.
 * Strong written and verbal communication, organizational, and problem-solving skills.
 * Proficiency in Python, R, Perl, SQL, or other programming languages, together with familiarity with APIs and Linux/Unix environments.
 * Fluent English language skills, both written and verbal.

Preferred Qualifications

 * Degree concentration in Biology or a related life sciences discipline.
 * Experience supporting precision medicine, biomarker operations, laboratory data management, or biosample logistics within clinical trials.
 * Familiarity with laboratory information management systems (LIMS), specialty laboratory databases, and clinical data transfer processes.
 * Experience working with global clinical study teams, specialty vendors, and laboratory operations across multiple studies.

## Description

We are seeking an experienced Programming Lead, Samples, Kits and Laboratory to support precision medicine initiatives across global clinical development programs. This role serves as a key technical and operational partner, driving the management, oversight, and optimization of biomarker samples, laboratory operations, kit logistics, and associated data throughout the clinical trial lifecycle.

Working cross-functionally with clinical study teams, data management, biostatistics, laboratory vendors, and operational stakeholders, you will play a critical role in ensuring high-quality sample management, laboratory data integrity, and operational excellence. Your expertise will help advance precision medicine strategies that support the development of innovative therapies for patients worldwide., * Participate in cross-functional study teams to support and deliver precision medicine strategies across assigned clinical studies.

 * Serve as a subject matter expert for technical and operational aspects of sample management, testing activities, and biomarker-related study operations.
 * Lead the planning, tracking, and oversight of biomarker samples, kits, laboratory operations, logistics, and associated data throughout the study lifecycle.
 * Develop tools and dashboards that support tracking of samples, kits, laboratory data, and operational metrics within precision medicine programs.
 * Use programming tools and technologies to aggregate, extract, process, and assess study data in accordance with industry standards and study requirements.
 * Support the development and review of sample-related content for study documents, including protocols, informed consent forms, and sample management guidelines.
 * Collaborate with data management and biostatistics teams to define biomarker data capture, transfer, reporting, and database requirements.
 * Review laboratory databases, resolve biomarker data queries, and support database lock activities to ensure data quality and compliance.
 * Manage operational activities related to biosample storage, shipping, testing, data transfers, budgeting, reporting, and vendor oversight.
 * Help ensure human sample management processes meet protocol requirements, standard operating procedures, and applicable regulatory standards.