Remote Programming Lead – Biomarker Samples & Logistics

Parexel; United States; A distancia; GBP 65.000 - 90.000; Jornada completa

Descripción de la vacante

Parexel is seeking a physician-science oriented professional to support precision medicine studies. The role involves cross-functional study team participation, subject-matter expertise in sample management, and development of study documents related to biospecimens.

You will oversee biosample planning, data transfer, and biomarker sample testing while coordinating with vendors and clinical teams to ensure protocol compliance and data integrity throughout the study lifecycle.

Formación

• Minimum of 6 years clinical research experience with academic, CRO, pharma or biotech industry.
• Bachelor degree in life sciences or equivalent; Biology or related major preferred.
• Fluent in speaking/writing English; strong communication skills.

Responsabilidades

• Participates in cross-functional study team meetings to support precision medicine delivery.
• Supports clinical study teams on sample management and testing, including risk management and stakeholder queries.
• Develops and reviews sample-related sections of study documents (protocols, ICFs, sample management guidelines).
• Supports creation and validation of specialty laboratory databases for data collection and kit tracking.
• Manages biosample process planning, storage, shipping, and data transfer through study lifecycle.
• Oversees acquisition and testing of samples for biomarker research and defines contract scope with vendors.

Conocimientos

Project management

Analytical skills

Communication skills

English fluency

MS Office / Excel

Programming languages

Educación

Bachelor's degree in life sciences

Herramientas

Python/R/Perl/SQL

Linux/Unix environments

Descripción del empleo

Parexel is seeking a physician-science oriented professional to support precision medicine studies. The role involves cross-functional study team participation, subject-matter expertise in sample management, and development of study documents related to biospecimens.

You will oversee biosample planning, data transfer, and biomarker sample testing while coordinating with vendors and clinical teams to ensure protocol compliance and data integrity throughout the study lifecycle.