The Centralized Monitoring Analyst is responsible for setting up, programming, and refreshing the Centralized Monitoring platform to support study-specific quality and risk indicators. They work directly with clients to manage deliverables and ensure data quality through ongoing monitoring and assessment.
The VP of Global Sales will develop and execute a comprehensive commercial strategy to drive revenue growth and market expansion within the MedTech industry. They will lead a high-performing global team while building strategic relationships with C-suite executives and key decision-makers.
The Senior Project Set-Up Coordinator provides operational support for laboratory projects, including the design, configuration, and validation of databases within Clinical Trial Management Systems. They are responsible for maintaining project documentation, coordinating internal meetings, and ensuring all activities comply with established procedures and regulatory standards.
The epidemiologist will lead the design and implementation of real-world studies, including drug safety and effectiveness research, using common data models like OMOP. They will also author study protocols, review statistical analysis plans, and provide epidemiological expertise to cross-functional teams and clients.
The Data Analyst will perform data analytics activities to provide insights for business problems and support internal project teams. Responsibilities include updating and maintaining databases, ensuring data accuracy, and identifying trends or anomalies in projected data.
The role involves reviewing clinical and safety data to ensure medical accuracy and completeness while supporting study start-up activities. You will collaborate with study physicians to evaluate medical cases and contribute to the development of patient narratives and safety processes.
Lead cross-functional clinical trial teams and guide assigned studies from planning through execution and reporting, ensuring quality, timely delivery, patient recruitment, and clinical data objectives. Manage study budgets and resource allocation, embed risk management and contingency planning, and promote operational excellence and knowledge sharing.
Conduct in-home visits with clinical trial patients to collect samples, monitor vitals, and administer medications. Document adverse events and ensure accurate reporting of clinical trial data.
Conduct in-home visits with clinical trial patients to collect samples, monitor vitals, and administer medications. Document adverse events and ensure accurate reporting of clinical trial data.
The Clinical Project Manager is responsible for the planning, implementation, and execution of clinical trials while managing project teams and maintaining client relationships. They ensure compliance with SOPs, ICH GCP guidelines, and FDA regulations while overseeing project timelines and budgets.
The Clinical Trial Nurse conducts in-home visits to collect samples, administer medications, and monitor patient safety during clinical trials. They are responsible for documenting adverse events and ensuring accurate reporting of clinical data.
Conduct in-home visits with clinical trial patients to collect samples, monitor vitals, and administer medications. Document adverse events and ensure accurate reporting of clinical trial data.
The Associate Consultant supports the design and delivery of patient-focused and outcomes research projects for healthcare clients. They are responsible for conducting qualitative and quantitative research, synthesizing evidence, and managing cross-functional stakeholders to develop client-ready deliverables.
Conduct in-home visits with clinical trial patients to collect samples, monitor vitals, and administer medications. Document adverse events and ensure accurate reporting of clinical trial data.
Conduct in-home visits with clinical trial patients to collect samples, monitor vitals, and administer medications. Document adverse events and ensure accurate reporting of clinical trial data.
The Associate Consultant will analyze market trends, build forecasting models, and develop strategic insights for the IVD and Diabetes testing markets. They will also support client-facing projects, conduct industry expert interviews, and ensure the quality of junior consultant outputs.
The Contracts Manager will review, draft, and redline commercial service contracts while ensuring alignment with IQVIA business objectives. They will independently manage high-volume legal reviews and communicate concerns to relevant stakeholders.
Manage laboratory-related aspects of clinical trial projects from startup through closeout while partnering with project managers. Coordinate day-to-day activities, monitor project status, and maintain clear communication with clients to ensure high-quality execution.
Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead study set-up, monitor project timelines and budgets, and coordinate cross-functional resources to ensure high-quality execution.
Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead study set-up, monitor project timelines and budgets, and coordinate cross-functional resources to ensure high-quality execution.
The Business Development Manager will prospect and secure new business within the MedTech and medical device industry by building relationships with key decision-makers. They will lead the end-to-end sales process, including solution positioning, proposal development, and contract negotiations to meet client needs.
The role involves providing medical safety expertise, conducting signal detection, and performing medical evaluations of adverse drug reactions. The director will also contribute to periodic aggregate reports, risk management plans, and provide safety oversight for clinical trials and post-marketing activities.
The Senior Clinical Investigator Payment Associate manages accurate and timely clinical site payments while ensuring compliance with contracts and budgets. They also serve as a primary point of contact for investigative sites and internal stakeholders to resolve payment discrepancies and support financial forecasting.
The Clinical Investigator Payment Associate manages accurate and timely payments to clinical sites in accordance with Clinical Trial Agreements and budgets. They are responsible for reconciling transactions, maintaining audit-ready documentation, and collaborating with internal and external stakeholders to resolve payment-related issues.
Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead study set-up, monitor project timelines and budgets, and coordinate cross-functional resources to ensure high-quality, customer-focused execution.
The Virtual Patient Educator provides education and resources to patients regarding specific diabetes treatments and prescribed medications. They conduct one-on-one communications via telephone, video, email, and SMS while maintaining strict program guidelines.
The Solution Implementation Lead oversees the end-to-end execution, development, and operationalization of connected medical device and digital health solutions. This role coordinates cross-functional teams and manages startup plans to ensure solutions are ready for scalable study deployment.
The role involves administering, scoring, and reviewing psychiatric assessments such as MINI and MADRS for a depression study. You will act as a Central Independent Rater to support clinical trial data integrity and patient outcomes.
The Field Service Coordinator facilitates and tracks daily activities to ensure field service needs are met on time and in accordance with organizational goals. They act as the primary point of contact for healthcare facilities to coordinate assignments and manage customer expectations.
Define the product vision and roadmaps for agentic AI initiatives to streamline clinical trial workflows. Lead multiple early-stage projects by collaborating with engineering and clinical teams to drive rapid experimentation and scaling.
