Project Manager- CARDIOVASCULAR (US/CANADA)

Worldwide Clinical Trials4 Locationsonsite$112k–$222kView the original posting at Worldwide Clinical Trials ↗

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. Join us! Make an Impact as a Project Manager at Worldwide Lead clinical trials that span Phase I through IV studies and help drive successful outcomes from study start-up through closeout. In this role, you'll take full ownership of assigned projects, coordinating cross-functional teams and ensuring studies are delivered on time, within scope, and to the expected quality standards. You'll collaborate with internal experts, external partners, and sponsors to navigate complex challenges, manage resources effectively, and keep projects moving forward. Your leadership will play an important role in delivering high-quality clinical research that supports the advancement of new therapies. Working across local, regional, and global studies, you'll have the opportunity to influence strategy, solve problems proactively, and help teams achieve project and customer objectives. Where You'll Work This is a REMOTE role open to candidates based in US, CANADA. You will collaborate with global teams across multiple time zones. Some domestic and international travel, including overnight stays, will be required. What You'll Do Lead cross-functional project teams to successfully deliver Phase I-IV clinical trials from start-up through closeout Direct the operational, technical, and financial aspects of assigned projects to achieve study objectives Coordinate internal functions, external customers, and subcontractors to ensure seamless project execution Develop, maintain, and adapt project plans while proactively identifying risks and implementing mitigation strategies Partner with functional leaders to define resource requirements and establish contingency plans for critical project needs Monitor project progress, resolve challenges, and drive solutions that support quality, timeline, and budget expectations Foster collaboration, accountability, and effective teamwork across matrixed project teams Communicate project status, risks, and key developments to leadership and stakeholders Ensure all project deliverables align with customer expectations, contractual commitments, and quality standards What You'll Bring University or college degree in a life science discipline preferred, or certification in a related allied health profession, or an equivalent combination of education and experience Minimum 5 years of clinical pharmaceutical industry experience, including demonstrated clinical project management expertise Alternatively, 5+ years of supervisory experience in a healthcare setting combined with 4 years of clinical research experience in the pharmaceutical or CRO industry, or equivalent demonstrated clinical development experience Thorough knowledge of project management methodologies and processes Strong understanding of ICH Guidelines, Good Clinical Practice (GCP), and internationa

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