Worldwide Clinical Trials

Senior Project Manager - Oncology - US/Canada - Remote

Worldwide Clinical Trials$128K — $254K *
US-Anywhere
+ 2 other locationsRemote
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 6-7 years' industry experience, with at least 5 years in Clinical Project Management at a CRO.
  • Required oncology experience in project management.
  • Preferred degree in Life Sciences.
  • Strong project management process knowledge, including budget management.
  • Ability to travel as needed.

Responsibilities

  • Coordinate and manage clinical trials from start-up to closeout.
  • Direct all technical, financial, and operational aspects of projects for successful trial completion.
  • Evaluate project issues with functional area leads to interpret data and implement solutions.
  • Ensure all deliverables align with customer expectations regarding time, quality, and cost.
  • Collaborate with Project Management Directors and functional leads to meet customer and contract expectations.

Benefits

  • Commitment to an inclusive and equitable workplace.
  • Competitive benefits package depending on location.
Full 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 which will not only give you an opportunity to develop in depth global operational expertise, but also benefit from exceptional scientific and medical background that our experts bring. 

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 budge.

  • Can demonstrate experience of successfully managing and/or leading multidisciplinary project teams.

Your experience 

  • 6-7 years' industry experience with a minimum of 5 years in a Clinical Project Management role, within a CRO setting. 

  • Oncology experience in a PM role is required. 

  • University/College degree, within Life Science is preferred. 

  • Ability to travel when needed 

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):


United States of America - $128,500.00 - $254,500.00


The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

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
Founded
1986

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