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Oversee end-to-end clinical study delivery, including study plans, vendors and CROs, country progress, budgets, supplies, risks, and cross-functional team communications. Maintain inspection readiness through oversight of study data and eTMF completeness, while resolving or escalating delivery issues and mentoring colleagues.
Lead end-to-end clinical data management start-up, including protocol review, study specifications, database configuration, testing, validation, and production go-live. Coordinate cross-functional stakeholders, manage timelines and changes, and ensure documentation and deliverables meet SOP, ICH-GCP, regulatory, and quality requirements.
The Creative Operations Associate will coordinate project workflows, manage production logistics, and maintain internal systems to support the creative team. They are responsible for organizing digital assets, managing vendor relationships, and implementing process improvements to enhance operational efficiency.
The Senior Clinical Team Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor study performance, and ensure compliance with ICH GCP and regulatory standards.
The Document Review Specialist is responsible for reviewing Informed Consent Forms and patient recruiting materials to ensure compliance with regulatory requirements and GCP guidelines. They also manage the filing of documentation in TMF/eTMF and provide input for CAPA activities related to document review.
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You will own the end-to-end influencer and affiliate revenue engine, from sourcing and recruitment to commission structures and performance reporting. You are responsible for managing relationships with creators and partners to drive scalable revenue and pipeline growth.
The Senior Global Study Manager acts as the primary liaison between clients, CROs, and internal teams to ensure seamless study delivery. They provide project management oversight, manage complex global study portfolios, and ensure all deliverables meet quality and regulatory standards.
The Project Administrative Assistant will manage the administrative and financial aspects of COA licensing projects, including budget tracking and invoice coordination. They will also maintain project data, generate status reports, and liaise with internal and external stakeholders to ensure timely project delivery.
Act as the first point of contact for customers facing technical challenges with broadband, mobile networks, and TV apps. Resolve issues using internal tools or coordinate on-site technician visits while identifying commercial opportunities to improve customer satisfaction.
You will coordinate QA activities across complex Salesforce projects, acting as the primary point of contact between internal teams and external providers. Your role involves managing test evidence, overseeing defect lifecycles, and ensuring all quality gates are met for delivery acceptance.
The role involves drafting, reviewing, and negotiating clinical research site contracts and budgets with investigators and sponsors. You will also liaise with legal and regulatory teams to ensure compliance and facilitate the execution of agreements.
The Senior Change Orders Associate manages the budget development lifecycle for clinical change orders by collaborating with operational, finance, and business development teams. They are responsible for preparing resource and service fees, ensuring accurate budget timelines, and presenting budgets to stakeholders as needed.
The Project Budget Coordinator will manage clinical trial budgets, track indirect costs, and provide financial reporting for project teams. They will also coordinate cross-functional activities and handle purchase requisitions within the clinical supplies lifecycle.
The Associate Data Manager assists in maintaining clean clinical trial databases by reviewing data and ensuring protocol compliance. They also support the development of CRFs, edit check specifications, and perform user acceptance testing for study deliverables.
The Head of Affiliates & Agents is responsible for owning the partner acquisition strategy, managing the P&L, and leading the affiliate and agent teams. This role involves driving growth through market expansion, deal negotiation, and rigorous performance management of partner networks.
Advise clients on market entry, business strategy, and cultural navigation within Chinese markets and European diaspora communities. Represent projects in meetings across Europe and maintain a network of partners and stakeholders.
Lead and manage the strategic, operational, and financial delivery of site activation activities across assigned studies and regions. Collaborate with internal and external stakeholders to ensure efficient study start-up, regulatory compliance, and timely patient enrollment.
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Coordinate global artwork creation and modification projects from initial brief through to final approval while ensuring regulatory and strategic alignment. Act as a central point of contact for cross-functional teams including Regulatory, Marketing, R&D, and Graphic Design to ensure project timelines and quality standards are met.
The Senior Site Specialist will manage operational activities for investigator sites across the Benelux region, including site start-up, maintenance, and regulatory documentation. They will act as a primary liaison for site staff and provide mentorship to junior team members to ensure efficient study execution.
Manage hotel, flight, and car rental bookings while coordinating payments and verifying invoices with providers. Provide support to the Trip Planner team and troubleshoot issues to ensure a seamless client experience.
Manages complex translation project lifecycles, including planning, scheduling, and risk management. Facilitates communication between project teams and clients while ensuring financial and administrative processes are completed.
The Study Manager is responsible for the end-to-end delivery, governance, and performance of site engagement activities across assigned clinical trials. They lead cross-functional coordination, analyze site performance data, and serve as the primary point of contact for sponsors and clinical teams.
The Qualified Person for Pharmacovigilance acts as the EU/UK QPPV for selected clients, ensuring compliance with EU Directive 2001/83/EC and associated regulatory guidance. They also contribute to scientific safety services, manage budgets, and promote QPPV services to potential clients.
The AdOps Specialist is responsible for implementing and optimizing ad setups on client websites to maximize revenue. They must identify and resolve technical issues while ensuring data accuracy and providing comprehensive reporting to clients.
The Senior Associate is responsible for supporting Real-world Evidence services by delivering complex analyses of data from global observational studies and secondary sources. They will develop analysis-ready datasets, create tables, figures, and listings, and provide programming support to biostatisticians and epidemiologists.
The Statistical Scientist will contribute to study design, statistical analysis, and programming for Real World Evidence projects. They will also support scientific communication activities, including publications and conference presentations, while collaborating with cross-functional teams.
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Act as the primary point of contact for customers of an online pet supply store via phone and email. Identify and communicate technical issues to the supervision team while providing professional guidance on products and orders.
The CIO will define and execute a global technology strategy to support the university's mission, operational excellence, and international growth. They are responsible for leading a distributed team and overseeing product management, software engineering, data analytics, AI transformation, and cybersecurity.
Interns will conduct literature reviews and prepare research summaries, issue notes, and analytical briefs on policy, legal, or human rights topics. They are also responsible for drafting a supervised research paper or policy report while meeting deadlines in a remote environment.
The Media Monitoring Specialist validates media content, produces editorial summaries, and maintains search strategies to ensure high-quality client deliverables. They also collaborate with cross-functional teams to analyze data and provide actionable insights through reports and dashboards.
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