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The Clinical Data Manager acts as the primary data lead for global clinical trials, overseeing study start-up, data review, and database lock activities. They ensure regulatory compliance and drive operational excellence while managing cross-functional study teams and sponsor partnerships.
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 management. They are responsible for ensuring study integrity, managing site relationships, and guiding teams on patient recruitment and protocol compliance.
The Clinical Trial Manager will oversee clinical trials and programs, managing external vendors and contract research organizations to ensure efficient execution. They are responsible for study documentation, regulatory compliance, and providing leadership to clinical research associates.
The Senior Clinical Trial Manager will oversee complex Phase I-IV clinical trials, managing CROs, vendors, and global clinical operations teams to ensure operational excellence. They are responsible for study planning, regulatory compliance, financial tracking, and coordinating cross-functional teams to deliver high-quality clinical research.
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The recruiter is responsible for identifying, engaging, and delivering qualified candidates through full-cycle recruitment activities. They will collaborate with account managers to build talent pipelines and ensure a positive candidate experience throughout the hiring process.
The Senior Decentralized Clinical Trial Study Lead is responsible for the strategic development and delivery of decentralized clinical trials, ensuring they meet quality, speed, and financial objectives. They act as the primary point of contact for customers and lead cross-functional teams to manage study milestones, risks, and project performance.
Lead complex clinical trial projects and regulatory submissions while managing client meetings and cross-functional collaborations. Develop statistical analysis plans, provide expert biostatistical consulting, and support data safety monitoring boards.
Lead data management activities across assigned studies from start-up through database lock and close-out. Perform EDC data review, data cleaning, and reconciliation of external data sources while partnering with study teams to resolve data issues.
The virtual assistant will manage patient communications, including phone calls and emails, while assisting with medication refill requests and scheduling inquiries. Additionally, the role involves maintaining standard operating procedures to support the practice's transition to a cash-based model.
The Senior Biostatistician will independently create randomization schedules, develop statistical analysis plans, and lead clinical trial projects across various phases. They will also collaborate with sponsors, regulatory teams, and programmers to ensure high-quality statistical outputs and regulatory compliance.
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The specialist will research and identify government grant opportunities in the US and Canada while managing the full lifecycle of applications. They are responsible for writing high-quality proposals, liaising with stakeholders, and maintaining accurate records of the grant pipeline.
The Clinical Operations Lead provides oversight of project deliverables, CRAs, and investigator sites to ensure compliance with protocols and regulations. They act as the primary liaison between the monitoring team and the clinical project team while managing site performance and recruitment strategies.
Manage and execute day-to-day operational activities for clinical trials in accordance with ICH/GCP and regulatory guidelines. Lead clinical operations for early and late phase trials, including budget control, vendor selection, and mentoring of clinical staff.
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Provide dedicated 1:1 support to the Managing Director by managing calendars, travel, and communications. Streamline business operations through administrative support, report preparation, and internal process improvements.
The Associate will conduct market and landscape research to develop value propositions and go-to-market strategies for medicines in Low- and Middle-Income Countries. They will also prepare high-quality client deliverables and support stakeholder engagement to advance global health initiatives.
Coordinate day-to-day operations, compliance, and financial administration for a UK-based dental group. Monitor staff rotas, track clinical KPIs, and manage patient communication workflows.
Manage a caseload of clients through virtual communication systems to provide nutritional support for medically supported weight loss. Coordinate care with doctors and create personalized, evidence-based content to help clients manage obesity and related chronic conditions.
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