As a Global Study Manager/ Project Manager, you will lead or contribute to one or more cross-functional global working groups and Study Teams, which deliver all operational aspects of one or more studies through all phases and stages. Responsibilities: - Drive Operational excellence by developing operational plans, creating and managing clinical study budget and overseeing the consistency of operations- Manage vendor and stakeholders by managing relationships with vendors and cross-functional stakeholders. Oversee performance of vendors and third-party providers -Lead and influence by establishing yourself as a leader within the team, being recognized as a thought leader who inspires others to perform at their best and learn from best practices. You’ll be shaping our capabilities and evolving your role overtime- Manage risk and compliance by developing site monitoring and risk mitigation strategies and ensuring your team adheres to all appropriate standards, including ICH/GCP and other regulations- Plan demand and supply by overseeing the resource management, forecast and maintenance of supplies needed to ensure sites have the necessary supplies to run clinical studies- Provide country oversight by leading feasibility assessments to ensure countries and sites are selected for participation in trials. Provide guidance to country operational reps during trials You are:Talented and passionate. Here at PRA we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
Have a growth mindset and are excited about learning through experience
Feel comfortable thinking on your feet and thrive in fast-paced, ambiguous and highly collaborative environments
Have a minimum 3 years of relevant experience like clinical trial management or project management experience
Hold a university degree or equivalent years of experience, preferred focus in life sciences
A self-starter who finds passion in achieving successful outcomes by leading, directing and inspiring peers
Want to make a difference and find excitement in innovating practices, products and processes
Possess strong working knowledge of drug development process and respective regulations, including ICH and GCP guidelines
Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better. PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.
