Lead and oversee Project Directors and Project Managers to plan, execute and govern global clinical study projects in autoimmune, ensuring quality, scope, cost and timeline objectives. Requires a bachelor's in a science/health field (advanced degree preferred), minimum 10 years clinical research experience, working knowledge of GCP/ICH, experience in pharmaceutical/device research, proficiency with Microsoft Office and Microsoft Project, people management experience, and willingness to travel domestically and internationally.

Lead clinical logistics projects including supply, sourcing, manufacturing, distribution, and laboratory logistics for biopharmaceutical studies. Responsible for project scope, timelines, budgets, resource allocation, client liaison, vendor management, regulatory compliance (ICH GCP, GCLP, GMP, GDP), and process improvement initiatives.

Lead company-level strategic initiatives and the Product & R&D operating system (intake, prioritization, launch, post-release feedback). Translate strategy into execution, align senior stakeholders across functions, represent product vision externally, and drive measurable outcomes. Requires ~8+ years experience in Product Operations, Product Management, Strategy & Operations or similar roles.

The Local Study Associate Director (LSAD) for Peru remotely leads Local Study Team(s) to ensure timely, compliant delivery of clinical study commitments. Key responsibilities include site identification/qualification, oversight of monitoring from activation to closure, regulatory and EC/IRB submissions, CTMS and eTMF management, budget and agreement preparation, risk management, and training/coaching of local study staff. Minimum required experience is 3 years in Development Operations (CRA/SrCRA) or related fields; proficiency in English and fluency in local language(s) are required.

Permanent Programme Manager role with Equal Experts based in South Africa. No further details provided (description: TBC).

The Program Manager will manage the full project lifecycle and enforce PMO processes, providing portfolio-level oversight, consolidated reporting, resource and vendor management, risk and issue escalation, budgeting support, stakeholder engagement, and ensuring smooth transition to BAU for enterprise applications (e.g., SAP, CRM).

The Engagement Manager, Professional Services at GitLab scopes outcome-oriented services engagements, conducts discovery with customers and account teams, builds proposals and statements of work, coordinates with delivery and operations (including staffing and time zone/language coverage), manages forecasting in Salesforce and Clari, and supports commercial discussions to drive deal closure. Role is remote (US-based salary range listed).

The Local Study Associate Director leads Local Study Team(s) at the country level to ensure sites are qualified, set up, initiated, monitored and closed in compliance with client SOPs, ICH-GCP and local regulations. Responsibilities include CTMS and eTMF management, regulatory and IRB/EC submissions, budget and agreement preparation, patient recruitment support, risk management, team leadership and coordination with global stakeholders. Requires minimum 3 years' relevant experience and proficiency in English.

Local Study Associate Director responsible for country-level delivery of clinical study activities including site identification/qualification, initiation, monitoring and closure; maintaining CTMS/eTMF, coordinating regulatory and ethics submissions, managing budgets and vendor relationships, developing risk plans and reporting to global study leadership. Requires a minimum of 3 years' relevant experience and proficiency in English.

Responsible for implementing eClinical platforms for studies, gathering and documenting requirements, configuring systems (CTMS, EDMS, EDC, IVRS), coordinating global virtual teams, managing client communications, ensuring compliance with SOPs/ICH-GCP/21 CFR Part 11, and supporting timely, high-quality delivery. Role can be fully home based in Romania, Serbia, Poland, or South Africa.

Regional Director of Professional Services (Americas) responsible for driving bookings and PS revenue through sales partnership and pre-sales engagement; executing partner-first co-delivery models; owning delivery operations, utilization, margin, and CSAT targets; and managing and developing a regional delivery team. Requires 10+ years in professional services (including 5+ years in senior leadership), experience with partner ecosystems, and familiarity with IAM/cybersecurity/cloud. Travel within the Americas up to 30%.

Remote Senior Executive Assistant role supporting the SVP, Global Customer Solutions at Grafana Labs. Combines high-level executive support (calendar, travel, expenses, meeting coordination, confidential communications) with hands-on program management responsibilities (tracking programs, driving cross-functional accountability, preparing leadership materials). Role favors experience in tech/high-growth environments, comfort with AI/automation tools, and working in PST or MST time zones. US-based compensation range listed.

The role manages the clinical data management process from study start-up through post database lock, including CRF specification, database build and UAT, edit checks, medical coding, AE/SAE reconciliation, vendor liaison, and training. Candidates should have 5+ years (Clinical Data Manager II) or 8+ years (Senior CDM) relevant experience; oncology experience and database migration experience are preferred. Position is remote with candidates considered in the UK, Poland, Hungary, Romania, Serbia, or Slovakia and may require occasional travel.

Remote role supporting clinical data management across assigned studies from start-up to post-database lock, including CRF/spec development, database build and UAT, edit checks, query and data entry oversight, medical coding and SAE/AE reconciliation. Candidates may be based in the UK, Poland, Hungary, Romania, Serbia or Slovakia. Requires professional English and 5+ years (Clinical Data Manager II) or 8+ years (Senior CDM) relevant experience; occasional travel may be required.

The Clinical Data Manager II/Senior Clinical Data Manager will manage all aspects of clinical trial data management for assigned projects, including CRF specification, database build and UAT, edit checks, medical coding, SAE/AE reconciliation, vendor coordination, documentation for the TMF, and training. Requires 5+ years as a Clinical Data Manager II or 8+ years as a Senior Clinical Data Manager; occasional travel may be required. Oncology experience and SAS familiarity are preferred.

The Business Operations Associate reports to the VP of Business Operations and will drive strategic planning (including OKRs), conduct research and analysis to support leadership decisions, improve processes and knowledge sharing (Notion as SSOT), and coordinate company-wide activities such as all-hands and offsites. Requires 3–6 years of relevant experience, strong stakeholder management, analytical skills, comfort with macOS and remote collaboration tools, and authorization to work from the US or Canada. US cash compensation range listed as $109,000–$125,000.

Lead and govern large-scale, cross-functional AI transformation programmes across Delivery and GTM, including establishing Nearform’s AI Centre of Excellence in Ireland. Responsibilities include programme governance, integrated planning, risk and dependency management, change management and adoption, workforce planning and talent strategy, and executive reporting. Requires 10+ years experience in large-scale transformation (technology/consulting/digital services), exposure to AI/ML concepts, strong data literacy, and senior stakeholder communication skills.

The Investigator Grants Associate II provides grant administration and financial support to project and finance teams, focusing on site payment tracking, CTA review, advance balance tracking, reconciliations, and relevant reporting (e.g., Sunshine Act, MMSE). Requires ~3 years clinical research experience, accounts payable background, and professional English proficiency.

Responsible for coordinating customer onboarding and ongoing program initiatives for SIEMaaS, developing and managing project plans, tracking milestones, facilitating status updates and executive communications, identifying and driving resolution of risks and blockers, and ensuring alignment across sales, product, professional services, and contractor partners (ECS Federal). Role focuses on stakeholder communication, resource coordination, and continuous improvement of onboarding processes.

Role responsible for the strategy, governance, configuration, QA, and launch processes for event platforms, registration, mobile apps, onsite technology, data flows into Salesforce/Tableau, and scalable operational frameworks. Requires hands-on experience with major event tech platforms, strong data and reporting skills, vendor management, and the ability to build templates, runbooks, and automation to scale event execution.