Barrington James

www.barringtonjames.com

4 Jobs

421 Employees

About the Company

The global Life Sciences industry is dominant in today's world. Drug development processes are progressing faster than ever before. The need for vaccines, treatments and medical devices continues to grow at an exponential rate to ensure treatment for disease reaches those it needs to.

That means for Barrington James, we grow at the same speed. With 14 global offices specialising in niche areas of the Life Science industry, we are ready to support our growing group of clients in sourcing the most, senior, specialist and rare candidates to join them.

'We Invest In Our People' through training and development, through meritocratic progression, and through unrivalled commission structures, shareholder and bonus schemes.

Barrington James Board & Executive Partners
Barrington James is your global and award- winning Life Science Executive recruitment partner. With combined experience of over 100 years, our Executive Search team has access to the deepest pharmaceutical networks.

Our primary focus is to understand and address the business challenges and hiring needs of our clients through a range of bespoke services, including Executive Search, Project Management, Market Research, Mapping Practice and Reference Check Insights.

Listed Jobs

Company Name: Barrington James
Job Title: Software Team Lead-Cutting-Edge Technology (Quantum)
Job Description: Job title: Software Team Lead‑Cutting‑Edge Technology (Quantum) Role Summary: Lead, mentor, and architect software solutions for quantum‑enabled systems, driving technical vision and team performance in a fast‑paced R&D environment. Expectations: - 8+ years software development, 4+ years in a formal leadership role. - Demonstrated ability to build scalable, high‑performance systems. - Strong communicator who can translate complex concepts to diverse audiences. Key Responsibilities: - Direct a team of engineers to deliver innovative, scalable software. - Drive architecture design and implementation of quantum‑related software stacks. - Mentor team members, set performance goals, and foster a collaborative culture. - Coordinate with cross‑functional stakeholders to ensure seamless technology integration. - Align engineering initiatives with overarching product strategy and business objectives. Required Skills: - Proficient in Python and modern software architecture patterns. - Experience designing and deploying scalable, maintainable systems. - Exposure to quantum computing or quantum‑adjacent technologies. - Leadership experience: coaching, goal setting, performance management. - Strong written and verbal communication skills, capable of explaining technical topics to non‑technical audiences. Required Education & Certifications: - Bachelor’s or Master’s degree in Computer Science, Software Engineering, Physics, or related field. - Relevant certifications (e.g., AWS Certified Developer, Microsoft Certified: Azure Developer) are a plus.

Company Name: Barrington James
Job Title: Freelance HEOR Oncology Director
Job Description: Job title: Freelance HEOR Oncology Director Role Summary: Lead the ownership, coordination, and execution of the company’s first Joint Clinical Assessment (JCA) dossier for an ex‑US oncology asset. Provide strategic oversight of evidence synthesis, HTA alignment, and cross‑functional collaboration with Market Access, Medical Affairs, Clinical Development, and Biostatistics. Expectation: - Remote work throughout Europe, with occasional travel to Paris. - Commit 2–3 days per week. - Start ASAP; initial contract through September, with potential extension. Key Responsibilities: - Prepare and assemble the JCA dossier, managing timelines, governance, and cross‑functional input. - Oversee vendor‑led evidence synthesis and statistical workstreams. - Guide PICO‑driven systematic literature reviews and payer advisory materials. - Supervise development of Statistical Analysis Plans and indirect treatment comparisons. - Evaluate feasibility for Real‑World Evidence initiatives. - Provide early‑stage cost‑effectiveness modeling direction. - Serve as the central HEOR liaison for ex‑US cross‑functional teams. Required Skills: - Solid oncology expertise, ideally in rare or targeted therapies. - Proven experience leading JCA or major EU HTA submissions. - In‑depth knowledge of the EU HTA framework and evolving requirements. - Strong vendor management and stakeholder alignment capabilities. - Ability to operate in lean environments and establish processes. - Strategic mindset with strong subject‑matter expertise. Required Education & Certifications: - Advanced degree (MSc, PhD, or equivalent) in Oncology, Epidemiology, Biostatistics, Health Economics, or related field. - Professional certification or membership in relevant HEOR or oncology professional societies (e.g., AACB, CEOMA) preferred.

Suresnes, France

Remote

10-03-2026

Company Name: Barrington James
Job Title: Business Operations Manager
Job Description: Job Title: Business Operations Manager Role Summary: Lead and coordinate day‑to‑day business operations for the UK & Ireland team in a life sciences environment, ensuring efficient, compliant processes and supporting cross‑functional initiatives such as meetings, events, and marketing materials. Expactations: - Deliver reliable operational support to multiple internal teams. - Maintain high standards of compliance and internal process adherence. - Manage logistics for meetings, congresses, and internal events. - Oversee contract, invoice, and purchase order processing. - Collaborate with external partners and vendors. Key Responsibilities: - Support smooth daily business operations across the region. - Plan and coordinate logistics for meetings, congresses, and internal events. - Provide administrative and operational support to multiple teams. - Manage contracts, invoices, and purchase orders. - Ensure compliance with internal processes and regulatory requirements. - Develop and distribute marketing and operational materials. - Maintain inventory and lifecycle management of materials, including version control and reprints. - Coordinate with external partners and vendors. - Work cross‑functionally with Marketing, Finance, Market Access, and Medical teams. Required Skills: - Minimum 5 years experience in business operations, office management, or similar role. - Strong organisational and project management abilities. - Excellent written and verbal communication. - Ability to manage multiple priorities independently. - Experience supporting cross‑functional teams and multiple stakeholders. - Proficiency in Microsoft Office. - Knowledge of CRM systems, contract management, and finance processes preferred. - Experience in life sciences, healthcare, or regulated industry preferred. - Comfortable working in a fast‑paced, dynamic environment. Required Education & Certifications: - Bachelor’s degree or equivalent work experience. ---

England, United kingdom

Hybrid

11-03-2026

Company Name: Barrington James
Job Title: Quality Assurance Consultant
Job Description: Job title: Quality Assurance Consultant Role Summary: Provide expert quality assurance for clinical trials, ensuring adherence to Good Manufacturing Practice (GMP) and regulatory standards through audits, documentation review, and corrective action coordination. Expactations: - Deliver accurate, timely audit findings and quality reports. - Maintain consistent compliance with GMP and local regulations. - Foster collaboration across clinical operations, regulatory, and medical teams. - Support a culture of continuous quality improvement. Key Responsibilities: - Lead internal and external audits of clinical trials, verifying GMP and regulatory compliance. - Review protocols, CRFs, informed consent documents, and regulatory submissions for accuracy and completeness. - Identify, document, and track deviations and quality issues; recommend corrective and preventive actions. - Collaborate with clinical operations, regulatory, and medical teams to address quality concerns. - Participate in vendor and site audits when required. - Maintain QA documentation, produce management reports, and prepare materials for regulatory inspections. Required Skills: - Strong knowledge of GMP, clinical trial regulations, and quality management. - Proficient audit planning, execution, and reporting. - Excellent analytical, problem‑solving, and documentation skills. - Effective communication and stakeholder collaboration. Required Education & Certifications: - Bachelor’s degree in Life Sciences, Pharmacy, Biology, or related field (or equivalent experience). - Relevant GMP or regulatory certification preferred (e.g., Certified Quality Auditor, GMP credential).

Brussels, Belgium

On site

13-03-2026