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

Parexel; United States; Remote; USD 120,000 - 170,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Vacation/Holiday/Sick Time

Flexible benefit portal

Car or car allowance

Job summary

Parexel is seeking an experienced Programming Lead, Samples, Kits and Laboratory to advance precision medicine across global clinical programs. You will oversee biomarker sample operations, kit logistics, and data integrity from study design through database lock.

You will collaborate with data management, biostatistics, and vendors to deliver high-quality data and compliant laboratory processes, contributing to patient-focused therapies worldwide.

Qualifications

• Bachelor’s degree in Life Sciences or equivalent; biology or related major preferred.
• Minimum of 6 years of clinical research experience in academic, CRO, pharma, or biotech.
• Knowledge of clinical drug development, clinical databases, ICH-GCP, and FDA/local regulations.
• Proficiency with Microsoft Office, especially Excel, and role-specific systems.
• Strong written and verbal communication, organizational, and problem-solving skills.
• Proficiency in Python, R, Perl, SQL or similar, and familiarity with APIs and Linux/Unix.
• Fluent English, written and spoken.

Responsibilities

• Participate in cross-functional study teams to support precision medicine strategies across assigned clinical studies.
• Serve as SME for biomarker sample management, testing activities, and biomarker-related study operations.
• Lead planning, tracking, and oversight of biomarker samples, kits, laboratory operations, logistics, and data throughout the study lifecycle.
• Develop tools and dashboards that track samples, kits, laboratory data, and operational metrics.
• Use programming tools to aggregate, extract, process, and assess study data per industry standards and study requirements.
• Support development and review of sample-related content for study documents (protocols, informed consent forms, etc.).
• Collaborate with data management and biostatistics to define biomarker data capture, transfer, reporting, and database requirements.
• Review laboratory databases, resolve biomarker data queries, and support database lock activities.
• Manage biosample storage, shipping, testing, data transfers, budgeting, reporting, and vendor oversight.
• Ensure human sample management meets SOPs and regulatory standards.

Skills

Python

R

SQL

APIs

Linux/Unix

Excel

Communications

English

Education

Bachelor’s degree in Life Sciences

Biology or related major preferred

Tools

LIMS

Laboratory databases

Job description

When our values align, there’s no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world’s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we’re committed to making a difference.

About Parexel

Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose, moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry-leading innovation, With Heart®.

About the Role

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.

Key Responsibilities

• 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.

Candidate Profile

You’ll thrive in this role if you bring:

• 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.

Required Qualifications

• 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.

Benefits and Compensation

• Health, Vision & Dental Insurance
• Vacation/Holiday/Sick Time
• Flexible benefit portal
• Car or car allowance (only applicable roles)

We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research and help bring innovative treatments to patients around the world.