The Talent Acquisition Coordinator builds a talent pipeline, assesses candidate suitability, maintains candidate records, and engages with community employment groups.

Provide administrative support to the Clinical Project Management department including document management, scheduling, and clerical services to ensure efficient operation.

Manage financial planning and analysis operations by preparing budgets, analyzing data, enhancing product efficiency, and supervising staff to ensure high-quality service delivery.

A Senior Statistician applies biostatistical methods to support clinical trials, overseeing statistical analysis and collaborating with project teams for data management and reporting.

The Product Support Specialist provides technical support, triages issues, and maintains a knowledge base to enhance product performance and user experience.

Manage IT projects by planning, executing, and ensuring adherence to methodologies. Oversee team performance, vendor management and ensure compliance with industry standards.

Responsible for programming in SAS, creating variables, data extraction, debugging, and supporting statistical models for clinical and pharmaceutical projects.

The Statistician is responsible for applying biostatistical methods to support clinical trials, perform data management, and provide statistical expertise throughout the project life cycle.

As a Senior Quality & Compliance Auditor, you will lead audits, ensure regulatory compliance, and develop training programs in clinical research contexts.

Lead Database Programmer responsible for building, testing, and maintaining clinical study databases. Provides mentorship to team members and communicates project progress to stakeholders.

The Senior Quality & Compliance Auditor leads audit planning and execution, ensuring compliance with GxP guidelines and regulatory requirements in clinical research activities. Responsibilities include developing audit strategies, conducting audits, and implementing corrective actions while training and guiding teams on quality assurance processes.

Support development and monitoring of Quality Management Systems, assist in audits, and manage quality assurance training programs.

The Quality Associate/Specialist oversees technology quality management processes, ensuring compliance and identifying continuous improvement opportunities in clinical research.

The Country Manager oversees clinical trial operations, engages with investigators and vendors, ensures compliance, and leads regional operational activities.

The Country Manager oversees clinical trial operations, ensuring compliance with regulations, managing project deliverables, and liaising with investigators and vendors. The role includes leading regulatory submissions and financial processes for clinical trials across the designated region.

Lead the planning, management, and oversight of clinical trials in a country, ensuring compliance and effective collaboration with various stakeholders.

The Country Manager oversees clinical trial operations in a region, ensuring compliance and managing relationships with investigators and vendors, while supporting operational functions and project management.

The Study Start Up Specialist supports project management, regulatory and legal activities for clinical site start-up. Responsibilities include document preparation, contract negotiation, tracking site intelligence, and maintaining relationships with study sites to meet start-up timelines.

Coordinate all start-up activities for clinical studies, collaborating with various teams to ensure timely completion of necessary documents and regulations.

The Study Start Up Specialist coordinates site start-up activities, manages documentation, negotiates contracts, and ensures project timelines while maintaining relationships with clinical sites.