Top Tech Jobs & Startup Jobs in Manchester

The Manager, Sales Effectiveness drives revenue growth by enhancing sales performance, implementing tools, managing Salesforce effectiveness, and collaborating with Sales and Marketing teams.

A mid-level C# .Net Back End Software Engineer responsible for the software development lifecycle, collaborating with teams, and maintaining software applications with a focus on Azure cloud services.

The Senior Programmer Analyst leads statistical programming for analyzing real-world data, ensuring high-quality deliverables that support evidence generation and regulatory submissions, collaborating with various stakeholders in the healthcare industry.

Lead biostatistics contributions for commercial development, develop analysis plans for clinical trial data, and collaborate with cross-functional teams. Manage data analysis and ensure quality deliverables while communicating findings effectively.

Lead web merchandising and Digital Sales initiatives for Thermo Fisher Scientific, focusing on customer experience and data-driven strategies. Collaborate with various teams to enhance digital marketing capabilities and run multifaceted campaigns.

Provide legal advice and support for drafting, reviewing and negotiating contracts, while handling legal concerns and improving processes.

Manage sales for Biosciences products in Central London, achieve sales targets, maintain customer accounts, and collaborate with internal teams.

The role involves coordinating clinical monitoring and site management, ensuring compliance with protocols, managing documentation, and fostering relationships with investigational sites.

The Assistant Clinical Research Associate at Thermo Fisher Scientific supports clinical trials by assisting with site management, monitoring tasks, and logistical support while ensuring compliance with regulations. Responsibilities include managing study activities, supporting training, coordinating site supplies, and verifying documents.

Coordinate and oversee clinical monitoring activities for international Phase 2/3 studies, ensuring compliance with GCP and regulatory standards while managing relationships with CROs.