Senior Project Manager -Oncology- US - Remote

Worldwide Clinical Trials Holdings, Inc.

North Carolina

Hybrid

USD 100,000 - 150,000

Full time

14 days+
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Job summary

Worldwide Clinical Trials is seeking a seasoned Senior Project Manager to lead clinical trials from start-up through closeout, coordinating technical, financial, and operational aspects to ensure quality and compliance. You will guide cross-functional teams and client stakeholders to keep programs on time and on budget.

The role emphasizes accountability, proactive problem-solving, and doing it right the first time in a global CRO environment; travel as needed and collaboration with science and

Qualifications

  • Proven ability to lead multidisciplinary project teams.
  • Strong communication with clinical and business stakeholders.
  • Demonstrated budget, risk and change-control management.

Responsibilities

  • Senior Project Manager 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.

Skills

Communication skills
Travel readiness
Under pressure
Budget management
Leadership
Problem solving

Education

Life Science degree

Tools

MS Office

Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

What the Project Management department does at Worldwide

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 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.

For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We're on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity.

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 other class protected by applicable law.

We're a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever. We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we're here, you'll get a different answer. And that's what makes us special.

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