Lead day-to-day clinical monitoring delivery, particularly for European CRAs, overseeing staffing, resource planning, training, performance, compliance, and continuous improvement. Coordinate with sponsors, research partners, project teams, and independent contractors to support study delivery, resolve concerns, maintain quality, and meet regulatory and service requirements.
Lead and execute all data management activities for assigned projects, ensuring data integrity and reliability from study start-up through database lock. Supervise team members, manage project resources, and act as a subject matter expert to support process improvements and departmental goals.
The Senior Clinical Data Manager leads the planning and execution of data management activities, ensuring data integrity and validity throughout the study lifecycle. They also supervise team members, provide mentorship, and act as a Subject Matter Expert to drive process improvements and regulatory compliance.
The HR Generalist provides operational and administrative support across various HR functions including talent management, employee relations, and total rewards in a global context. They are responsible for managing onboarding, performance management processes, health and safety compliance, and maintaining accurate HR data.
The Talent Acquisition Specialist is responsible for supporting global full-cycle recruitment, including sourcing, screening, and interviewing candidates. They also manage offer negotiations, maintain talent pipelines, and contribute to employer branding and HR projects.
The Image Service Coordinator assists in the execution of image services activities, ensuring data integrity and reliability according to regulatory standards. They provide ongoing support to clinical sites and sponsors while performing quality assurance activities to ensure accuracy and completeness.
The TMF Associate is responsible for managing Trial Master File content and processes throughout the study lifecycle to ensure inspection readiness. They will collaborate with cross-functional teams, perform quality control, and provide training to stakeholders to maintain document integrity.
Provide administrative and project coordination support, including managing documents and records, coordinating meetings and training, and assisting with billing and payment activities. Serve as the first point of contact for project queries and maintain project materials and processes in accordance with project requirements, quality standards, and regulatory guidelines.
Provide administrative and project support, including managing, reviewing, tracking, filing, and retrieving paper and electronic documents in accordance with project, corporate, industry, and regulatory standards. Coordinate meetings, travel, correspondence, records, and inquiries; maintain tracking databases, prepare reports, and contribute to improving document management processes.
Independently manage clinical site monitoring and site management activities across Portugal and Spain throughout the study lifecycle. Ensure investigative sites comply with protocols, ICH-GCP, and regulatory requirements while providing mentorship to junior staff.
The Proposal Specialist supports the Business Development team by preparing high-quality clinical trial budgets, proposals, and Statements of Work. They collaborate with cross-functional teams and subject matter experts to ensure accurate, competitive, and timely responses to sponsor requirements.
The Director provides leadership and oversight for global clinical trial execution, including project management and financial reporting. They also participate in senior leadership strategy development, staff performance management, and business development activities.
The Director provides leadership and oversight for global clinical trial activities, including project management and financial operations. They also participate in senior leadership to develop organizational strategies, manage staff performance, and support business development initiatives.
The Clinical Database Programmer will design, build, and maintain clinical study databases within EDC systems, including configuring eCRFs and edit checks. They will also collaborate with project teams to support data integrations, validation activities, and the implementation of innovative AI-driven solutions.
The Information Security Analyst will identify vulnerabilities, monitor threats, and strengthen security controls across cloud and infrastructure platforms. They will also contribute to compliance, audit readiness, and incident response to reduce organizational risk.
The Database Programmer designs, develops, and maintains clinical study databases throughout the study lifecycle. They also program custom functions using C# and support the deployment of Medidata Rave EDC.
The ServiceNow Platform Specialist will administer, configure, and develop the ServiceNow platform to support IT Service Management and workflow automation. They will collaborate with stakeholders to translate business requirements into scalable technical solutions while ensuring system stability and security.
Lead validation activities for GCP-regulated computerized systems, from planning and documentation through testing, release, and post-execution management. Coordinate with IT, Quality Assurance, business stakeholders, and vendors to manage testing issues, support change control, and maintain ongoing regulatory compliance.
The Senior Clinical Research Associate will independently manage clinical site monitoring and site management activities across Croatia, Serbia, and Bosnia. They are responsible for ensuring protocol compliance, maintaining study documentation, and providing mentorship to junior team members.
Oversee regional clinical project planning and delivery, ensuring studies meet sponsor expectations, timelines, budgets, quality standards, and regulatory requirements. Manage sponsor relationships, project resources, risks, vendors, and team development while contributing to proposals, business development, and continuous improvement.
The Clinical Project Manager leads the planning, execution, and monitoring of clinical research projects to ensure objectives and regulatory standards are met. They coordinate cross-functional teams and serve as the primary point of contact for sponsors to manage project timelines, budgets, and deliverables.
The manager is responsible for planning, managing, and evaluating the daily delivery of the Clinical Monitoring unit while ensuring regulatory compliance and high-quality service. They also oversee staff resource planning, performance management, and third-party contractor coordination throughout the project life cycle.
The manager is responsible for planning, organizing, and evaluating the daily delivery of the Clinical Monitoring unit while ensuring regulatory compliance and high-quality service. They also manage staff resources, contractor performance, and collaborate with internal and external stakeholders to drive process improvements.
The Senior Integration Developer will design, build, and maintain robust integration solutions using Azure and AWS services to connect business and clinical platforms. They will also implement monitoring, automation, and security protocols while providing technical leadership and guidance to junior team members.
The Lead Data Engineer will design, build, and operationalize scalable data solutions while driving automation and integration across the Azure ecosystem. They will provide technical leadership, mentor junior staff, and ensure data governance compliance across enterprise analytics initiatives.
Lead accounting operations across accounts payable, accounts receivable, procurement, general ledger activities, and reconciliations while ensuring accurate, timely, and well-controlled financial processes. Develop the accounting operations team, improve and scale processes through automation, monitor financial risks and metrics, and provide analysis and reporting to senior leaders and business stakeholders.
The Senior Clinical Research Associate independently performs and oversees clinical site monitoring activities to ensure protocol and regulatory compliance. They serve as the primary liaison between sponsors and investigative sites while mentoring junior staff and supporting site recruitment and setup.
The Senior Clinical Research Associate independently performs and oversees clinical site monitoring, ensuring protocol and regulatory compliance. They serve as the primary liaison between sponsors and investigative sites while mentoring junior staff and managing site recruitment and setup activities.
The developer will manage the software development lifecycle from design to implementation, focusing on imaging products and cross-functional collaboration. Responsibilities also include providing technical support, performing code reviews, and authoring comprehensive technical documentation.
The Senior Clinical Research Associate will act as a subject matter expert, providing mentorship and performance feedback to peers while overseeing site monitoring and study integrity. They will also manage monitoring services for complex projects, assist in hiring and training, and serve as the primary escalation point for site or patient issues.
