Senior Project Manager -Oncology- US - Remote

Worldwide Clinical Trials

Milwaukee (WI)

On-site

USD 90,000 - 120,000

Full time

14 days+

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Job summary

Worldwide Clinical Trials is looking for a Senior Project Manager based in Milwaukee, WI. The role involves overall management of clinical trials, ensuring project deliverables meet expectations, and leading cross-functional teams. The ideal candidate will have 6-7 years in the industry with at least 5 years in clinical project management roles. A degree in Life Sciences is preferred. The position requires excellent communication skills, accountability, and proficiency in project management processes.

Qualifications

  • 6-7 years in the industry with at least 5 years in Clinical Project Management.
  • Demonstrated ability to travel when needed.
  • High level of responsibility and accountability.

Responsibilities

  • Coordinate and manage clinical trials from start-up to closeout.
  • Direct the technical, financial, and operational aspects of projects.
  • Work with functional area leads to resolve project issues.
  • Ensure deliverables meet time, quality, and cost expectations.

Skills

Communication skills
Project management processes
Budget management
Multidisciplinary team leadership
MS Office proficiency

Education

University/College degree in Life Sciences

Job description

What The Project Management Department Does At Worldwide

Worldwide Clinical Trials Project management is the perfect blend of operational rigor and therapeutic expertise, with a client‑focused approach. Our Global Project Leads (GPLs) and Clinical Project Managers (CPMs) expertly guide our project teams to deliver with high quality, focusing on “doing it right the first time”.

The Project Management team is engaged in all aspects of the trial, collaborating with scientific and therapeutic leadership, coordinating across project teams, and providing flexible, innovative and proactive solutions. At Worldwide, you will be dedicated to a specific therapeutic area, giving you an opportunity to develop in‑depth global operational expertise and benefit from an exceptional scientific and medical background.

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.
  • Direct the technical, financial and operational aspects of the projects—thus securing the successful completion of clinical trials.
  • Work 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.
  • Ensure all project deliverables meet the customer’s time/quality/cost expectations.
  • With support from the Project Management Directors, collaborate with other functional area leads to ensure 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.
  • Strong 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.
  • Demonstrated experience successfully managing and/or leading multidisciplinary project teams.
  • Proficiency in computer skills, including familiarity with relevant software and applications (MS Office).
Your Experience
  • 6‑7 years in the industry with a minimum of 5 years in a Clinical Project Management role within a CRO setting.
  • University/College degree, preferably within Life Sciences.
  • Ability to travel when needed.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or any other class protected by applicable law.

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