Responsible for conducting feasibility analyses, site and country assessments, site identification and outreach, recruitment and enrollment modelling, and presenting findings to business development and clients. Requires a life sciences bachelor's degree, a minimum of 5 years' related experience, professional-level English, and experience with data platforms and MS Office; ICH-GCP knowledge is expected.

Responsible for delivering feasibility deliverables including pre-award RFP input, protocol and assumptions review, site and country analysis, recruitment/enrollment modelling, site identification and outreach, and presenting feasibility recommendations to BD/clients. Requires a life sciences bachelor's degree and a minimum of 5 years' related experience; English professional proficiency and knowledge of ICH-GCP. Role can be covered remotely in the UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.

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.

Role involves reviewing, drafting, negotiating and tracking site Clinical Trial Agreements, vendor and other client contracts; coordinating with Clinical Operations and study teams to meet timelines; maintaining contract files and metrics; and contributing to contracting policies and process improvements. Requires a 4-year degree and at least 5 years' relevant experience in CRO/healthcare contracting.

Responsible for security and IT diligence of potential acquisitions/partnerships, leading integration of IT systems and security practices, driving technical workstreams across M&A transactions, and improving workflows via automation and AI-enabled tooling. Requires 4+ years of relevant experience and deep expertise in at least one area such as IAM, application security, DevOps/SRE, or cloud security.

Responsible for leading client solutions and business development, delivering regulatory outsourcing projects on time and within budget, and mentoring project leaders and teams. Requires a university degree in a scientific/technical discipline, extensive life sciences or consulting experience, proven regulatory affairs project leadership and business development skills, and fluent English.

Veeva seeks a remote Program Lead to oversee IT operations, release management, and post-implementation adoption for Veeva Vault R&D SaaS customers. The role is customer-facing, requires partnering with managed services, QA, IT and business teams, and involves occasional travel. Requires 8+ years of IT project/program management experience, strong communication skills, and familiarity with agile delivery; experience with Veeva Vault, data/content management tools (SharePoint, Smartsheet, Monday.com, Google Docs) and life sciences domains is desirable.

Netguru is hiring a Project Manager based in Poland to manage budgets, scope and timelines, report to stakeholders, coordinate design and software development, and maintain client relationships. Role requires at least 2.5 years managing agile IT projects, strong knowledge of Scrum/Kanban and tools like Jira/Pivotal Tracker, technical communication with development teams, and fluency in English (C1+) and Polish (C2). Posted salary ranges: PLN 7,700–12,000 gross/month (employment contract) and PLN 9,300–14,400/month (B2B).

Responsible for leading a multi-year, multi-phased global implementation program of Veeva Quality Cloud, acting as primary customer liaison, overseeing release management and IT operations, mentoring project teams, and guiding adoption of Quality Cloud and industry best practices. Requires 8+ years in IT project management/consulting/product management, experience with large enterprise implementations, technical affinity for software implementation, and willingness to travel 25-50%. Candidate must be legally authorized to work in the EU.

Remote (UK/Europe) manager role owning customer onboarding and integrations for Sardine’s fraud and risk platform. Responsibilities include leading the integration team, owning APIs and integration documentation, designing technical solutions, managing implementation projects, troubleshooting production issues, and providing product feedback. Requires 7+ years in implementations/integration/TA/solutions roles and experience with B2B SaaS domains such as payments, fraud, risk, or compliance.

Parexel is recruiting a Central Laboratory Vendor/Project Manager to support global clinical studies from the UK, Poland or Serbia. The role covers oversight of sample collection/processing/storage/shipping, vendor and CRO coordination, ICF/protocol review for sample sections, tracking and reporting of samples and data, and support through study set-up to close-out. Requires clinical research experience (6–8 years) and central laboratory and oncology experience.

Lead end-to-end delivery of web and mobile projects for connected devices (IoT, wearables). Act as single point of contact for US-based clients, manage cross-functional squads, run Scrum ceremonies, handle discovery, scoping, staffing, timelines and budgets, and use AI tools in daily workflow. Role requires 4+ years PM experience, hands-on delivery of custom software, familiarity with hardware-software trade-offs (firmware, OTA, certifications), and English at C1+.