Warman O'Brien

www.warmanobrien.com

2 Jobs

24 Employees

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: Senior Process Quality Excellence Specialist
Job Description: **Job Title:** Senior Process Quality Excellence Specialist **Role Summary** Provide expertise in SOP development, process improvement, and quality documentation for global pharmaceutical clinical studies. Deliver independent, cross‑functional SOPs and process documentation, supporting governance and risk management initiatives over a 12‑month contract. **Expectations** - 12‑month contract, 2 days per week on site (Slough). - Autonomously produce and revise SOPs aligned with global quality standards. - Collaborate with data management, risk management, and clinical research teams. **Key Responsibilities** - Draft, review, and update SOPs and supporting process documents for clinical studies. - Lead process improvement initiatives targeting efficiency, compliance, and risk mitigation. - Provide guidance and support to stakeholders on SOP application and best practices. - Ensure documentation meets regulatory and internal quality criteria across global programs. **Required Skills** - Extensive SOP writing and documentation experience. - Clinical research and data management knowledge, including risk and data standards frameworks. - Strong analytical and cross‑functional collaboration abilities. - Effective written and verbal communication in English. **Required Education & Certifications** - Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Engineering, or related field. - Professional certifications such as GCP, or Quality Management System (QMS) related credentials preferred but not mandatory.

Slough, United kingdom

Hybrid

Senior

25-11-2025

Company Name: Warman O'Brien
Job Title: Director Biostatistics
Job Description: Job title: Director – Biostatistics Role Summary: Lead independent statistical strategy for clinical, observational, biomarker, PK/PD, and regional projects in a global pharmaceutical environment. Act as subject‑matter expert, mentor junior statisticians, and ensure high‑quality data analysis and regulatory submission content. Expectations: Deliver expert statistical design and analysis for complex studies, maintain methodological rigor, collaborate cross‑functionally, and support continuous improvement of statistical practices. Key Responsibilities: - Serve as lead statistician for early and late‑phase clinical trials, observational research, and biomarker studies. - Provide strategic statistical input to study design, development plans, and decision‑making processes. - Mentor and guide study‑level statisticians; maintain high‑quality outputs across projects. - Prepare and review statistical sections for regulatory submissions, payer dossiers, and scientific publications. - Present data and findings to study teams and leadership. - Ensure integrated databases and external data sources support analysis and submissions. - Participate in due‑diligence, data review, and provide expert statistical advice. - Implement and validate advanced statistical methods; provide methodological oversight. - Identify and resolve statistical issues affecting data integrity and development decisions. - Contribute to improvements in statistical systems, processes, and standards. - Support recruitment, mentorship, and development of statistical staff. - Engage with external professional networks and collaborate on innovative methods. Required Skills: - Deep expertise in biostatistical methods for clinical and biomarker data. - Proficiency in SAS; R preferred. - Strong data management and programming knowledge. - Experience working with international teams and cross‑functional stakeholders. - Ability to translate complex statistical concepts for diverse audiences. Required Education & Certifications: - PhD or Master’s degree in Biostatistics, Statistics, or related scientific discipline. - Minimum 6 years of relevant experience with PhD (9+ years with Master’s), preferably in pharma, CRO, academia, or healthcare.

England, United kingdom

On site

Mid level

25-01-2026

Company Name: Warman O'Brien
Job Title: Senior Data Team Lead
Job Description: **Job Title:** Senior Data Team Lead **Role Summary:** Lead end‑to‑end data management (DM) services for large, multi‑country clinical trials (1,000+ patients), serving as the primary client liaison and overseeing a team of Data Team Leads. Drive process improvements, ensure delivery excellence from study start‑up through close‑out, and mentor DM staff. **Expectations:** - Minimum 15 years of data management experience in clinical research. - At least 10 years acting as an independent lead on global studies. - Proven track record delivering multiple large, multi‑regional trials. - Ability to negotiate timelines, budgets, and resources directly with clients. - Strong leadership, mentorship, and strategic influence skills. **Key Responsibilities:** - Oversee full‑cycle DM operations for multi‑country studies. - Lead, mentor, and develop a team of Data Team Leads and DM staff. - Define and implement process improvements and innovation initiatives. - Serve as primary client contact; negotiate project scope, timelines, and budgets. - Ensure data quality, regulatory compliance, and delivery excellence from start‑up to close‑out. - Collaborate with cross‑functional teams (e.g., biostatistics, clinical operations) to align data strategies. - Monitor project performance metrics and report status to stakeholders. **Required Skills:** - Expert knowledge of clinical data management processes, standards (CDISC, SDTM, ADaM), and regulatory requirements. - Strong project management and budgeting abilities. - Excellent client‑facing and negotiation skills. - Proven team leadership and staff development capabilities. - Proficiency with DM tools (e.g., Medidata Rave, Oracle Clinical, Veeva Vault) and data visualization/reporting tools. - Analytical thinking, problem‑solving, and decision‑making under pressure. - Effective communication (written and verbal) across global, virtual teams. **Required Education & Certifications:** - Bachelor’s degree in Life Sciences, Health Informatics, Computer Science, or a related field (Master’s preferred). - Relevant certifications such as Certified Clinical Data Manager (CCDM) or Project Management Professional (PMP) are advantageous.