The Platform & Automation Manager oversees automation operations, ensuring scalable solutions, compliance, and team support within an IT environment.

The Reg Affairs Specialist supports regulatory compliance by managing project deliverables, preparing documentation, liaising with clients, and ensuring adherence to guidelines.

The role involves preparing electronic regulatory submissions, ensuring compliance with regulations, and leading project-specific processes while mentoring junior staff.

As a Marketing Specialist II, you will enhance the digital customer experience, manage web content, analyze data, and collaborate with teams to drive improvement and optimize web pages using CMS and project management tools.

The Manager of Regulatory Affairs - CMC will prepare CMC packages for submissions and manage global change control assessments while ensuring compliance with regulations. They will provide regulatory strategy advice and lead project teams, ensuring high-quality standards and alignment with clients for effective project management.

The role involves authoring regulatory submissions, collaborating with departments, and managing compliance in CMC for biotech products.

The role involves ensuring timely delivery of quality regulatory submissions, managing projects, and leading quality reviews while mentoring staff and addressing sponsor needs.

This role manages global labeling activities, ensuring compliance with regulatory standards, and coordinates labeling processes across various markets while leading cross-functional initiatives.

The Regulatory Affairs Manager oversees global labeling processes, ensuring compliance with regulatory standards and managing submissions across markets. This role requires expertise in regulatory requirements and strong project management skills to coordinate labeling activities and support clinical trial regulations.

The Vendor Management Coordinator manages clinical supplies lifecycle, coordinates vendors, ensures compliance, and supports departmental project teams for studies.

The Sr Programmer Analyst will manage the configuration and maintenance of the Oracle Argus Safety database, developing reports and troubleshooting user queries. They will lead data migration projects and collaborate with business users on system requirements and enhancements.

The CRA performs clinical monitoring and site management, ensuring compliance with protocols and regulations. Responsibilities include monitoring sites, documenting observations, and managing relationships with investigators.

Supports project team in clinical trials by providing administrative and technical support, managing site activation, and contributing to feasibility assessments while maintaining audit readiness.

Lead all data management activities for clinical studies, mentoring junior staff, maintaining documentation, and ensuring compliance with protocols and regulatory guidelines.

As the Principal Medical Writer, you will produce high-quality medical writing, mentor writers, ensure compliance, and manage complex writing projects.

The Associate Manager Safety Data and PV Systems manages GPS Safety Data operations, supports Oracle Argus Safety system, collaborates with teams, and ensures compliance with regulatory standards.

The Analyst - Lab Informatics will configure, support, and enhance laboratory systems, ensuring compliance and efficient lab data workflows in regulated environments.

As a Senior Clinical Data Associate, you will manage data for projects, ensuring accuracy and compliance with protocols, while training junior staff and improving processes.

The Senior Clinical Data Associate supports data management projects, ensuring accuracy, compliance, and improvement of processes while mentoring junior staff.

The Sr Clinical Data Associate manages data for clinical trials, ensures data quality, trains junior staff, and improves data processes.