Senior Global Project Manager - US (CP11NC369)

Aixial Group • Greensboro, NC

14h • Remote

About The Position

The Aixial Group is in international Contract Research Organization (CRO), a member of the ALTEN Group, providing complex services in clinical trials (phase I-IV) and non-interventional studies. Our offices are located in France, UK, US, Belgium, Denmark, Sweden, Switzerland, Romania, and India.
We are currently looking for an enthusiastic and talented Senior Global Project Manager. This is a full-time permanent position that requires 1 FTE of availability. This role can be home-based in the US and will require about 10% of travel.

As a Global Project Manager, you will be responsible for managing and executing on small to large, global, complex, full-service clinical project(s) or multi-project programs. You'll work well alongside a project team, as well as independently to plan and deliver effectively. You are accountable for assessing and deliver on KPIs, including identifying project study trends, budgets, performance metrics and project reports.
The role as Global Project Manager requires high level of leadership with the ability to problem solve and day to day decision making while providing support to your project team members.

With proven global project management experience working within a CRO, Phase I-IV studies and profound knowledge of ICH-GCP, you will have the ability to understand, interpret and execute on key business and project deliverables. You are great at building relationships, have exceptional stakeholder management skills and you are an excellent communicator. You'll be managing client expectations, ensuring client satisfaction and will have a high impact role in a growing, dynamic, and successful CRO.

Requirements

• Substantial, proven experience as a Global Clinical Project Manager (required)
• Study finance management experience (required)
• Strong cross functional management skills (required)
• Strong problem solving, organizational and time management skills (required)
• Ability to develop and maintain positive, productive internal and external working relationships
• Bachelor's or equivalent combination of education and experience (required)

Nice To Haves

• Therapeutic area experience in early phase oncology, immunotherapies, CNS and/or radiopharmaceutical (therapeutic, diagnostic) research (desirable)
• Contract Research Organization (CRO) background (desirable)
• Strong and confident in bid defence meetings (desirable)

Responsibilities

• Plan and execute multiple phase I-IV studies to agreed timelines, scope, and budget, managing all aspects including overseeing vendors, to ensure patient safety, data integrity, and adherence to contract and protocol from study start-up to study closure.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 251-500 employees