Programming Lead – Samples, Kits, Data, Logistics

This is a fully remote position, open to applicants in Ireland.

📋 Description

• Engage in cross-functional study teams to facilitate and implement precision medicine strategies for designated clinical studies.

• Act as a subject matter expert on the technical and operational facets of sample management, testing procedures, and biomarker-related study operations.

• Oversee the planning, tracking, and management of biomarker samples, kits, laboratory operations, logistics, and related data throughout the study lifecycle.

• Create tools and dashboards to monitor samples, kits, laboratory data, and operational metrics.

• Utilize programming tools to compile, extract, process, and evaluate study data in accordance with industry standards and study specifications.

• Assist in the development and review of sample-related materials for protocols, informed consent documents, and sample management guidelines.

• Collaborate with data management and biostatistics teams on the capture, transfer, reporting, and database specifications for biomarker data.

• Examine laboratory databases, address biomarker data inquiries, and support activities related to database locking.

• Oversee biosample storage, shipping, testing, data transfers, budgeting, reporting, and vendor management.

• Ensure that human sample management procedures comply with protocols, SOPs, and regulatory standards.

⛳️ Requirements

• Bachelor's degree in Life Sciences or a related discipline such as Science, Technology, Engineering, or Mathematics, or equivalent professional experience.

• At least 6 years of clinical research experience within an academic institution, Contract Research Organization, pharmaceutical company, or biotechnology firm.

• Solid understanding of clinical drug development, clinical databases, ICH-GCP guidelines, and relevant regulatory requirements, including FDA and local country regulations where applicable.

• Proficient in Microsoft Office applications, particularly Excel, and familiar with role-specific systems.

• Excellent written and verbal communication skills, along with strong organizational and problem-solving abilities.

• Proficient in programming languages such as Python, R, Perl, SQL, or others, with a basic understanding of APIs and Linux/Unix environments.

• Fluent in English, both written and spoken.

• Experience in clinical research, biotechnology, pharmaceuticals, academia, or Contract Research Organizations.

• Comfortable working with laboratory databases, biomarker data, sample management processes, and technology platforms specific to the role.

🏝️ Benefits

• Health, Vision & Dental Insurance

• Vacation/Holiday/Sick Time

• Flexible benefit portal

• Car or car allowance (applicable to specific roles)

• Opportunities for flexibility and growth