Design and develop software solutions, focusing on Scala and Python. Collaborate on APIs, database management, and distributed data processing using Spark. Participate in Agile processes and system architecture discussions.

The Site Activation Specialist serves as a SPOC for clinical studies, overseeing regulatory compliance, site contracts, project timelines, and performance metrics, while ensuring all deliverables are met efficiently.

This role involves leading the preparation of safety aggregate reports, conducting literature surveillance, managing signals, and collaborating with regulatory bodies while ensuring compliance with safety standards.

Manage clinical studies, ensure compliance with protocols and SOPs, perform site monitoring, support project teams, and provide mentorship.

The Regional Specialist coordinates remote clinical visits, facilitates site and nurse onboarding, manages logistics and documentation, and ensures compliance with regulations, acting as the main liaison among sites, nurses, and internal teams.

The Consultant will develop and execute statistical analyses for real world studies, support project delivery, and communicate findings effectively.

The Client Relationship Associate will manage client relationships, drive business growth, and ensure exceptional client service while supporting sales initiatives.

The Associate Data Scientist will support antibody research through bioinformatics workflows, collaborate with teams, optimize methods, analyze data, and troubleshoot. Required qualifications include a PhD or MS with relevant experience.

The Project Manager leads clinical trial projects, ensuring delivery aligns with contractual requirements and optimizes quality and cost while collaborating with internal teams and clients.

The Senior Software Engineer will develop and maintain cloud-native full-stack applications, collaborate across teams, ensure software quality, and participate in code reviews.

The Statistical Programmer will create statistical outputs and visualizations using SAS and R, collaborate with cross-functional teams, assist in programming specifications, and ensure data quality for clinical trials.

Assist in clinical trial activities, including subject recruitment, scheduling, data management, and compliance with protocols and guidelines.

The role involves developing client relations and business opportunities, ensuring client satisfaction, managing proposals, and mentoring others, all while achieving revenue targets.

The MedTech Project Coordinator will manage customer remediation for field actions, coordinate projects, and support financial reporting, requiring strong project management and communication skills.

The role involves supporting market research projects, conducting data analysis, and assisting in client deliverables within the pharmaceutical sector.

The Bilingual Study Analyst supports project delivery for pharmaceutical clients through study document development, site selection, and data management, focusing on real-world evidence studies in Canada.

Lead cross-functional laboratory initiatives to improve efficiency and harmonize processes in ligand binding assay development. Provide technical leadership, troubleshooting support, and oversee method transfers. Contribute to SOP development and regulatory compliance.

This role involves designing and maintaining reporting templates, manipulating large datasets, and delivering insightful reports that inform healthcare service improvements.

In this role, you will lead consulting projects in life sciences, oversee business development, foster client relationships, and ensure high satisfaction. Responsibilities include leveraging insights for value and access strategies, presenting proposals, and enhancing team capabilities.

The Regional Contract Manager will support contract template maintenance, lead negotiations, conduct risk assessments, and provide guidance on contractual agreements.