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As a Clinical Research Associate, you will liaise with investigational sites, ensuring compliance, monitoring studies, maintaining documentation, and supporting recruitment efforts in oncology trials.

The Senior Clinical Research Associate manages monitoring for cardiovascular clinical trials, ensuring compliance with FDA regulations and guiding teams to resolve site issues effectively.

Senior-level network engineer providing highest-tier escalation for global network operations. Lead troubleshooting, major incident recovery, root-cause analysis, network design and delivery for enterprise projects, datacenter/cloud connectivity, security compliance, and automation across multi-vendor environments (Cisco ACI, Fortinet, F5, SD-WAN, Azure/AWS). Mentor junior engineers and support 24x7 mission-critical operations.

As a Global Study Manager, you will lead projects, manage cross-functional teams, and ensure successful project execution while mentoring team members.

Provide day-to-day HR support and guidance to employees and managers on employee relations, performance management, and policy interpretation. Assist in developing and implementing HR policies and initiatives, support recruitment and onboarding, collaborate on employee engagement and talent development projects, and maintain accurate records to ensure legal and regulatory compliance.

Manage marketing automation platforms to build and optimize email campaigns, customer journeys, lead scoring and nurturing. Integrate marketing automation with Salesforce CRM, develop dashboards/reporting, improve campaign performance, and train colleagues on processes.

Manage marketing automation and email campaigns, optimise lead nurturing and scoring, integrate marketing systems with Salesforce, build dashboards and reporting, support campaign execution (landing pages/forms), collaborate with sales, agencies, and designers, and document/train colleagues on automation tools and processes.

The Clinical Research Associate II will conduct site visits, ensure compliance and data integrity, collaborate with sites, and prepare study documents.

Oversee and manage clinical trials, ensuring compliance with timelines, budgets, and regulations while collaborating with cross-functional teams and stakeholders.

Manage negotiations and execution of clinical trial agreements and budgets independently, collaborating with sites and stakeholders to ensure efficient study start-up.