The Senior Business Analyst will elicit and document business and functional requirements, maintain requirements traceability, support UAT, facilitate stakeholder workshops, and translate business needs to technical teams. The role requires experience in regulated environments (pharma/CRO), familiarity with CSV, SDLC and 21 CFR Part 11, and domain knowledge of clinical trials. Generative AI experience is preferred. The position can be fully home based in the UK, Serbia, Romania, or Poland.

Netguru seeks a part-time freelance Business Intelligence expert skilled in QlikView (maintenance, development, data analysis). The role includes ad hoc and retainer-based support, BI solution migrations, and consulting on BI platform selection. Engagement is remote, starts August 2026, and is expected to last 3–6 months; rate from 40 EUR/hour. Candidate must be located in the European Union and have a good command of written and spoken English.

Senior Business Analyst based in Poland responsible for running discovery, translating business needs into testable requirements, mapping processes (BPMN/UML), identifying integration points across ERP/CRM/CMS/APIs, and validating technical solutions. Requires 5+ years in IT/technical BA roles, strong SQL and analytics skills, experience with Agile frameworks, and C1+ English.

Principal Clinical Business Analyst responsible for planning, designing, implementing and driving adoption of Business Operation Systems to support clinical study delivery. Requires ~8 years' relevant experience, expertise with clinical trial systems (CTMS, EDC, eTMF, RTMS), requirements gathering, configuration, integrations, testing/UAT, training, change management, stakeholder engagement and supporting audit/CAPA activities. Remote role based in Hungary, Poland, Romania, Serbia or Slovakia.

Lead the planning, design, development, implementation and adoption of Business Operation Systems to support clinical study delivery, including requirements gathering, configuration, testing (UAT), integrations, training and change management. Role requires experience with clinical trial systems (CTMS, EDC, eTMF, RTMS), experience in transforming business requirements into functional requirements, leadership experience, and effective English communication; Bachelor’s degree plus 8 years of relevant experience.

Principal Clinical Business Analyst responsible for planning, design, implementation and adoption of Business Operation Systems to support clinical study delivery. Role requires at least a bachelor's degree plus 8 years' relevant experience, expertise with clinical trial systems (CTMS, EDC, eTMF, RTMS), requirements gathering, configuration, integrations, UAT, training and change management. Salary estimate for Poland: 173,000 PLN - 259,400 PLN gross per annum.

Seeking a Principal Clinical Business Analyst with a minimum of 8 years' relevant experience to lead system implementation, requirements gathering, configuration, integrations, testing (including UAT), training and adoption for clinical trial systems (CTMS, EDC, eTMF, RTMS). Role is remote and based in Hungary, Poland, Romania, Serbia or Slovakia and requires effective English communication and experience in clinical operations and change management.

The Principal Clinical Business Analyst leads design, configuration, testing and adoption of clinical Business Operation Systems (e.g., CTMS, EDC, eTMF, RTMS). Responsibilities include requirements gathering, system implementation and integrations, UAT, training and change management, stakeholder engagement, audit/CAPA support, and using data/metrics to monitor adoption. Requires a bachelor's degree (or equivalent) plus 8 years of relevant experience and prior clinical operations/system experience.

Responsible for implementing eClinical technology for studies, including requirements gathering, design, configuration and integrations; primary contact for study technology with internal teams and external clients. Requires clinical trials experience, familiarity with CTMS/EDMS/EDC/IVRS, knowledge of CDISC SDTM, ICH-GCP and 21 CFR Part 11, and strong project/client management and communication skills.

Responsible for conducting feasibility analyses (competitive, recruitment, epidemiology, protocol review), site identification and outreach, enrollment modelling, and presenting recommendations to business development and clients. Requires a bachelor’s in life sciences, minimum 5 years' relevant experience, strong data/IT skills, and professional-level English. Knowledge of ICH-GCP and experience with oncology/rare disease trials preferred.

Role responsible for conducting feasibility analyses (pre- and post-award), site and country analysis, protocol review, recruitment and epidemiology analysis, site outreach, and enrollment modelling. Requires a bachelor's in life sciences (or equivalent), minimum 5 years' related experience, professional-level English, strong data/IT skills and familiarity with ICH-GCP. Remote in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.

Join Veeva as a Senior Consultant in Clinical Operations to configure and support Vault Clinical modules (e.g., eTMF, CTMS, SSU), lead implementations and post-implementation programs, liaise with customers and product teams, and drive change management. Position requires 8+ years' relevant experience, fluent English, and deep knowledge of Clinical Operations and ICH-GCP.

Responsible for implementing Veeva Quality suite and guiding life sciences customers on quality, compliance, and change management. Requires experience with quality management systems, document control, CAPA/Deviations/Change Control, customer-facing consulting, and strong English communication. Total compensation listed at 240,000–380,000 PLN. Candidates must be authorized to work in Hungary or Poland; employer does not anticipate visa sponsorship.