The Sales Representative will build partnerships with healthcare professionals, deliver scientific information, manage a diverse portfolio, and influence clinical decisions across the Southern Region of Chile.

The Senior Global Process Owner leads the design, governance, and continuous improvement of clinical study processes, ensuring compliance and efficiency, while managing risks and fostering cross-functional collaboration.

Oversee statistical programming and data analytics for drug development projects, ensuring quality, cost-efficiency, and compliance with timelines. Mentor associates and drive project-level standardization and solutions.

The Study Start-Up Lead coordinates global trial activities, ensuring timely document readiness and site activation, while leading the SSU team and managing vendor relations.

The Director will lead compliance risk management initiatives, conduct risk assessments, and enhance risk processes in healthcare.

The Analyst Clinical Label Management executes label design, ensures compliance with study requirements, manages documentation and reporting, and collaborates with internal and external stakeholders during clinical trials.

The GPRM develops and implements global regulatory strategies, coordinates submissions, and represents regulatory affairs across teams and regions.

The Payroll Services Expert will oversee payroll processes, coordinate data analysis, manage service requests, and improve payroll services by implementing standards and providing training.

The Study Start-Up Senior Lead manages global SSU activities for complex clinical trials, ensuring timely document completion and site activation, leading a multidisciplinary team, and overseeing project management to support efficient clinical trial processes.

As Head of Ethics, Risk, and Compliance, lead ethical practices, risk management, and compliance culture in a highly regulated environment while partnering with leadership teams.

The Associate Director leads a team in biotherapeutic engineering and bioconjugation, develops strategy, collaborates on therapeutic innovations, and ensures compliance with documentation and safety standards.

The Clinical Research Associate will manage site relationships, conduct monitoring activities for clinical trials, and ensure compliance with regulatory standards and protocols, focusing on patient recruitment and data integrity.

The Central Monitor oversees clinical trials through data surveillance, manages risks, collaborates with teams, and ensures compliance with GCP guidelines.

Lead the Regulatory Affairs function in Vietnam, ensuring compliance, strategic approvals, and collaboration with internal and external stakeholders for supply continuity and regulatory excellence.

The Product Specialist drives sales of oncology products, builds relationships with healthcare professionals, manages government business, and collaborates with hospitals to enhance product reach and adoption.

The role involves providing analytics support and driving data enablement initiatives to inform business decision-making in the pharmaceutical industry.

The role focuses on onboarding data for SIEM platforms, collaborating with various teams, and ensuring system stability with 24x7 on-call support. Key responsibilities include deploying security tools and managing customer onboarding requests.

The Supply Chain Manager oversees demand and supply planning for clinical supplies, ensuring project fulfillment and managing supply constraints while leading cross-functional teams.

Manage operations for digital finance analytics tools, ensuring optimal performance, user support, and process improvements in collaboration with stakeholders and technical teams.

The Lead Central Monitor oversees clinical trial monitoring by managing a team, developing strategies, ensuring data integrity, and fostering collaboration. They drive risk management and process improvements while supporting clinical trial teams in their execution.