Jobs at Worldwide Clinical Trials

Administers and maintains the global LMS, including course workflows, training assignments, user accounts, reporting, support documentation, security configurations, and audit records. Resolves user and system issues, coordinates with IT and vendors, supports compliance inspections, develops guidelines and FAQs, trains end users, mentors team members, and leads assigned training projects. The role requires strong LMS expertise, customer service, communication, organization, and knowledge of pharmaceutical or CRO environments.

Negotiate, draft, review, and finalize clinical trial site agreements and related contracts with UK sites. Responsibilities include negotiating contract language and budgets, reviewing study costs, quality-checking documents, coordinating with legal, privacy, study, sponsor, regulatory, and site teams, facilitating signatures, maintaining contract records, and preparing amendments or termination documents. The role requires clinical research or CRO experience, UK site negotiation expertise, regulatory knowledge, strong communication, analytical, and risk mitigation skills.

Coordinates global learning and development operations, including training logistics, calendars, learner communications, rosters, attendance tracking, materials, evaluations, and session closeout. Partners with facilitators, subject-matter experts, LMS administrators, People Partners, and business stakeholders to deliver virtual, hybrid, and in-person programs. Maintains training trackers, catalogs, SharePoint resources, and standardized workflows while identifying process improvements and supporting learning program planning across global time zones.

Leads European quality and compliance strategy for a global CRO, overseeing quality management, regulatory inspection readiness, audits, CAPA effectiveness, risk mitigation, and QMS governance. Provides executive-level guidance to clients and internal stakeholders, supports business development and regulatory activities, and leads quality transformation initiatives. Manages global quality teams and partners with senior leadership to ensure compliance with clinical research regulations and industry expectations.

Leads large, multinational clinical research projects and programs, ensuring delivery within cost, timeline, quality, and client expectations. Provides leadership, supervision, mentoring, and performance management for Project Managers; coordinates cross-functional teams, subcontractors, vendors, and clients; manages resources, budgets, risks, and project plans; supports proposals and business development; and drives process improvements aligned with clinical research standards and regulatory requirements.

Lead statistical design, analysis and reporting for clinical trials. Develop and validate SAS programs, produce SDTM/ADaM datasets, tables/figures/listings, write SAPs and reports, advise on study design, ensure regulatory compliance, and manage statistics support for sponsor projects.

Lead statistical support for clinical trials: design consultation, write and review SAPs, develop and validate SAS programs and CDISC datasets (SDTM/ADaM), produce tables/figures/listings, support reporting, QA, bids, and process improvements while ensuring regulatory compliance.

Support post-award site identification by developing site identification strategies, managing feasibility questionnaires, coordinating CDAs and outreach, recommending sites, training and overseeing Site Activation Specialists, and supporting remote teams. Travel under 10%.