Description

In this role, you will play a vital part in advancing clinical research by managing project documentation and coordinating supply chain activities. Your daily focus will involve collaborating with teams and clients to ensure the success of clinical trials while upholding quality standards.

Requirements

• •Bachelor's degree
• •Preferred fields of study: healthcare, supply chain management, life sciences, or related field
• •Project Management certification beneficial
• •Strong understanding of GMP/GxP principles and quality management systems
• •Demonstrated project management skills
• •Advanced proficiency in Microsoft Office suite
• •Experience with enterprise systems like Salesforce, GPMS, and TrackWise preferred
• •Strong analytical and problem-solving capabilities
• •Effective written and verbal communication skills
• •Detail-oriented with excellent organizational and documentation abilities
• •Ability to work independently and as part of cross-functional teams
• •Fluent English required, additional languages beneficial
• •Experience coordinating with teams and managing stakeholder relationships
• •Ability to analyze data and generate clear, accurate reports
• •Focus on quality service and continuous improvement
• •Adaptable to changing priorities while maintaining attention to detail
• •Travel to client sites or other facilities may be required

Tasks

• •Support clinical trials by managing project documentation
• •Coordinate supply chain activities
• •Ensure consistent delivery of services
• •Collaborate with internal teams and clients to support study success
• •Maintain the highest quality standards
• •Handle project planning and documentation management
• •Facilitate cross-functional coordination to meet timelines and client expectations

Tools & Technologies