JobsProject ManagerRaleighSenior Project Manager - Oncology (U.S., Canada)
Worldwide Clinical Trials
Posted 2 days ago · Jobs at Worldwide Clinical Trials
Senior Project Manager - Oncology (U.S., Canada)
Worldwide Clinical Trials · Durham, North Carolina, United States · also Ontario, Canada, North Carolina, United States
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In short
Lead cross-functional teams to manage Phase I–IV clinical trials from start-up through close-out while ensuring project scope, quality, and financial targets are met. Act as the primary client contact to build relationships, resolve challenges, and maintain alignment with program expectations.
What they're looking for
MUST-HAVE SKILLS
ALSO MENTIONED
Requires a university degree in life sciences or a related health profession and at least 7 years of clinical pharmaceutical industry experience. Candidates must possess thorough knowledge of ICH/GCP guidelines and demonstrated success in leading multidisciplinary project teams.
About the employer
Worldwide Clinical Trials
Worldwide Clinical Trials (Worldwide) is a global CRO serving development-driven biopharmaceutical companies, with more than 4,400 professionals operating across more than 70 countries. The company delivers therapeutically dedicated expertise in neuroscience, oncology, rare disease, and internal medicine, with comprehensive support across every development phase – from early-stage and first-in-human studies through Phase III registration trials.
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The company's flexible service model – spanning full-service trial management to functional service partnerships through Worldwide Flex – is powered by a people first, partnership driven outsourcing approach that strengthens collaboration, enhances data transparency, and supports more informed decision making. This provides sponsors with tailored, adaptable solutions that keep pace with the evolving demands of clinical research. Learn more at www.worldwide.com
- INDUSTRY
- Research Services
- COMPANY
- Privately Held
- HEADQUARTERS
- Research Triangle Park, NC
- SIZE
- 1,001-5,000
- OFFICES
- 11 on LinkedIn
- OPEN HERE
- 3 roles
KNOWN FOR
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Questions about this role
- Is this Worldwide Clinical Trials role remote?
- Tagged remote.
- What does it pay?
- The posting lists $128,500–$254,500 a year.
- Does it sponsor visas?
- Listed as no visa sponsorship.
- What experience does it ask for?
- Listed as 5-10 years.
The posting, in full
Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.
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Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.
With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research.
Make an Impact as a Senior Project Manager at Worldwide
Take ownership of complex Phase I–IV clinical trials and lead them from start-up through close-out. As a Senior Project Manager at Worldwide, you’ll be accountable for bringing together the people, plans, and resources needed to deliver successful local, regional, or global studies.
You’ll combine clinical project leadership with financial and operational oversight, partnering with cross-functional teams to solve challenges, manage risk, and keep programs aligned with client expectations for time, quality, and cost.
As a key client contact, you’ll also build strong relationships with client teams and vendors while creating an environment where multidisciplinary project teams can perform at their best.
Where You'll Work
This is a remote role open to candidates based in United States. You will collaborate with global teams across multiple time zones. Ability to travel 10% is required.
What You'll Do
- Lead core and extended cross-functional project teams, coordinating internal partners, clients, vendors, and subcontractors across assigned clinical trials.
- Manage Phase I–IV clinical trials from start-up through close-out, maintaining accountability for project scope, timelines, quality, cost, and delivery.
- Develop and maintain project plans, resource strategies, and contingency plans to support successful study execution.
- Drive financial performance by managing project budgets and working toward established financial targets.
- Partner with functional leads to evaluate complex project issues, interpret information, make sound business decisions, and implement effective solutions.
- Build strong client relationships as a key project contact, maintaining clear communication and helping ensure client expectations are met.
- Resolve project and team challenges through effective communication, negotiation, prioritization, and conflict management.
- Improve the efficiency and quality of project delivery while ensuring teams operate in accordance with established clinical research standards and SOPs.
What You'll Bring
- A university or college degree, preferably in life sciences, or certification in a related allied health profession such as nursing, medical technology, or laboratory technology; an equivalent combination of education and experience that provides the required knowledge and capabilities will also be considered.
- At least 7 years of clinical pharmaceutical industry experience, including demonstrated clinical project management skills and competencies; alternatively, more than 5 years of supervisory experience in a healthcare setting plus 6 years of clinical research experience in the pharmaceutical or CRO industries.
- Demonstrated success managing or leading multidisciplinary project teams, with thorough knowledge of project management processes and experience using project management software.
- Strong financial acumen, including an understanding of how to develop and manage project budgets, alongside effective negotiation and commercial skills.
- Thorough knowledge of ICH Guidelines and GCP, including international regulatory requirements for clinical development programs, and broad knowledge of the drug development process.
- Strong leadership, communication, organization, prioritization, and relationship-building skills, with the ability to work independently and effectively across cultures.
- Proficiency in English, written and verbal, as well as fluency in the local office language.
- Availability for domestic and international travel, including overnight stays, with a valid current passport and a valid driver’s license.
Discover the Difference
We love knowing that someone is going to have a better life because of the work we do. Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit http://www.worldwide.com/careers, or connect with us on LinkedIn.
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.
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.
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