Worldwide Clinical Trials

Senior Project Manager -Oncology- US - Remote

Worldwide Clinical Trials • $110K — $130K *
Research Triangle Park, NC 27709In-Person
Pharmaceuticals & Biotech
5 - 7 years of experience
Reposted Today
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Job Overview by Ladders

Qualifications

  • 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.
Learn more about Worldwide Clinical Trials
Size
1,500 employees
Industry
Healthcare
Founded
1986
* Ladders Estimates

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