6-7 years of industry experience, with at least 5 years in Clinical Project Management within a CRO
University/College degree in Life Sciences preferred
Proven capability to manage and lead multidisciplinary project teams
Thorough knowledge of project management processes and budget management
Strong communication skills
Ability to function effectively in high-pressure situations
Proficient in MS Office and relevant software applications
Responsibilities
Coordinate and manage clinical trials from start-up through closeout activities
Direct technical, financial, and operational aspects of clinical projects
Evaluate project fundamentals and interpret complex data
Ensure all project deliverables meet customer time, quality, and cost expectations
Collaborate with functional area leads to align project goals and expectations
Benefits
Opportunity to develop in-depth global operational expertise in a specific therapeutic area
Benefit from exceptional scientific and medical background from experts
Work in a client-focused environment with a strong team
Full Job Description
What you will do
Senior Project Manager (SPM) is responsible for the overall coordination and management of clinical trials from start-up through closeout activities.
Directs the technical, financial and operational aspects of the projects -- thus securing the successful completion of clinical trials.
Works with major functional area leads to identify and evaluate fundamental issues on the project, interpret data on complex issues, make good business decisions and ensure solutions are implemented.
Works to ensure that all project deliverables meet the customer's time/quality/cost expectations
The SPM, with support from the Project Management Directors, working in collaboration with other functional area leads, is accountable for ensuring that all project deliverables meet the customer/contract expectations.
What you will bring to the role
High level of responsibility and accountability in all tasks
Communication skills
Ability to effectively perform in demanding situations
Thorough knowledge of project management processes with a solid understanding of how to craft and manage a project budget
Can demonstrate experience of successfully managing and/or leading multidisciplinary project teams
Proficiency in computer skills, including familiarity with relevant software and application (MS Office)
Your experience
6-7 years' industry experience with a minimum of 5 years in a Clinical Project Management role, within a CRO setting
University/College degree, within Life Science is preferred
Ability to travel when needed
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
About Worldwide Clinical Trials
Worldwide Clinical Trials is a global contract research organization (CRO) that provides clinical research services to pharmaceutical and biotechnology companies. They specialize in early phase development, late phase development, and full-service clinical research. Worldwide Clinical Trials has experience in a wide range of therapeutic areas, including oncology, neuroscience, and infectious diseases. They are committed to providing high-quality, efficient, and cost-effective services to their clients.
