Global Project Manager

Emmes hires a Global Project Manager to lead the delivery of biopharmaceutical-sponsored clinical trials throughout the study lifecycle. The role manages client relationships, project teams, timelines, budgets, quality, risks, and deliverables.

Responsibilities:

• May serve as a primary lead for project bids and multi trial initiatives
• Ensures that deliverables for assigned projects are completed according to the contract budget, schedule, and quality standards. Effectively manages projects in all areas of performance
• Develops effective working relationships with clients, executive management, and project staff
• Collaborates with stakeholders to manage project issues, proactively identify and mitigate risks and drive milestone achievement
• Serves as the primary point of contact for biopharma clients. Demonstrates proficiency in knowledge and understanding of client needs
• Tracks project deliverables against contract using Emmes' tools. Proactively prepares presents study metrics to maintain transparency for internal external stakeholders
• Monitors trends and drives changes to the plan as needed; identifies risks to delivery and collaborates with the project team to develop mitigation plans to be presented to the client
• Ensures adherence to quality control expectations and milestone timelines for delivery of contractually required reports and deliverables
• Manages project resources i.e., budget, personnel, and subcontracts
• Identifies and manages change to scope and requests for out of scope activities
• Collaborates with Business Development, the Contracts Team, and executive management to ensure timely execution of contract amendments change orders
• Prospectively manages client expectations
• May present in bid defense meetings in collaboration with Business Development
• Develops study management plans in collaboration with core project team members
• Identifies and documents lessons learned from study successes and challenges to promote development of best practices
• Models and propagates Emmes' commitment to a culture of quality in all aspects of our deliverables, utilizing a solution based, science driven, value added approach in collaborating with clients
• Performs other duties as assigned
• Complies with all policies and standards

Requirements:

• Bachelor's Degree Scientific discipline
• 7-9 years Demonstrating scientific principles appropriate in managing a clinical research portfolio including multi-phase research experience in a broad range of indications and client types
• 1-3 years Pharmaceutical and/or CRO setting, serving in a global Trial Team Lead or Global Project Management role or equivalent position
• Demonstrable track record of success delivering complex and high priority clinical trials within agreed time, quality and cost working across multiple therapeutic areas, phases 1 to 4, in a global capacity
• Demonstrated experience in developing and fostering client and internal relationships
• Thorough understanding of ICH GCP and applicable global regulatory regulations and guidelines
• Skilled in MS Office Suite of products and working knowledge of Clinical Trial Management Systems, electronic Trial Master File, and electronic Data Capture systems and solutions
• Successful record in managing diverse staff and leading strong teams
• Strong verbal and written communication skills