Warman O'Brien

About the Company

Warman O'Brien is a global Life Sciences Recruitment partner, working across the UK, Europe, USA, and APAC.

We're proud to say that we have a 90% success rate of CV-to-interview matches, and our partnerships with pioneering Biotech, Pharma, and CROs across the USA, UK, Europe, and APAC. We recruit top talent across multiple functional areas, including Biometrics, Data Science, Quality Assurance, Regulatory Affairs, Clinical Research, Discovery Sciences, and Medical.

Roles we recruit for
Biostatisticians | Statistical (SAS & R) Programmers | MSL | Data Managers | Data Scientists | Bioinformaticians | Software Engineers | Clinical Research Associates | Clinical Project Managers | Translational Research | Product Characterisation | Discovery Sciences | Heads of and Directors of Departments | QA Managers | Qualified Persons | Regulatory Affairs and the C-Level role: CMO, CTO, CEO, COO, CSO.

Geographical Coverage
USA | UK | Europe | APAC

Service Offering
Permanent Recruitment | Contract Recruitment | Executive Search | Project and SOW Delivery

Our constant endeavour has been to effectively build a world leading network of candidates and clients. Since 2005, our consultants have been exhibiting our services and presenting our industry expertise at PhUSE, PSI, PharmaSUG and ASGCT.

info@warmanobrien.com | www.warmanobrien.com | +44 (0) 2033255075

Listed Jobs

Company Name

Warman O'Brien

Job Title

Medical Advisor

Job Description

**Job Title:** Medical Advisor **Role Summary:** Support the UK launch of a novel cardiovascular therapy for difficult-to-treat hypertension, requiring independent operation, external stakeholder engagement, and translation of complex clinical data into scientific insights. **Expectations:** Medical Affairs experience in cardiology; proven KOL engagement; understanding of UK healthcare/regulatory frameworks; launch experience; ability to interpret clinical data and deliver compliant medical inputs swiftly in a contract role. **Key Responsibilities:** - Lead external engagement with cardiology specialists and centers. - Translate clinical data into clear, educational scientific communications. - Contribute to launch strategy and medical planning. - Collaborate cross-functionally to drive market access and insights. - Develop compliant medical content aligned with UK standards. **Required Skills:** - Cardiology/CVD Medical Affairs expertise. - Stakeholder engagement and KOL relationship management. - Clinical data interpretation and scientific communication. - Cross-functional collaboration and project management. - UK healthcare regulatory compliance knowledge. - Autonomy, adaptability, and rapid delivery in high-pressure settings. **Required Education & Certifications:** - Medical degree (MD/PhD) or advanced clinical training in cardiology. - Relevant medical certifications (e.g., cardiology fellowship, UK licensing if applicable). - Proven experience in medical affairs or pharmaceutical launch support.

London, United kingdom

On site

18-03-2026

Company Name

Warman O'Brien

Job Title

Statistical Programmer

Job Description

Job Title: Statistical Programmer Role Summary: Lead statistical programming for oncology clinical trials, partnering with cross-functional teams to develop regulatory submissions and optimize programming standards, automation, and data workflows. Expectations: Provide technical leadership in SAS-based programming for SDTM/ADaM dataset development, TLF validation, and study deliverables, while mentoring teams and ensuring compliance with CDISC standards. Key Responsibilities: - Lead statistical programming across multiple clinical studies. - Develop, validate, and review SDTM and ADaM datasets per CDISC guidelines. - Generate and validate tables, lists, and figures (TLFs) for clinical reports and regulatory submissions. - Oversee programming standards, automation tools, and efficiency initiatives. - Author/review study plans (SAPs) and programming specifications. - Mentor technical teams and collaborate with biostatistics/data management. Required Skills: - Expert SAS programming in clinical trials, including CDISC (SDTM/ADaM) standards. - Proficiency in SQL and advanced SAS (STAT/Graph) for reporting. - Demonstrated leadership as a technical/study lead programmer. - Oncology clinical trial experience. - Background in CRO or pharmaceutical environments. Required Education & Certifications: Not specified.

United kingdom

Remote

26-03-2026