Project Manager – Rare Disease

🔥 35 minutes ago

🇨🇦 Canada – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 10%

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Lead cross-functional project teams and coordinate internal and external partners, including subcontractors, to deliver assigned clinical trials • Own project plans from start-up through close-out • Ensure deliverables meet agreed timelines, quality standards, budgets, and client expectations • Manage project resources with functional leaders, identifying needs and developing contingency plans • Oversee financial performance of assigned projects and work toward established financial targets • Anticipate project risks and complex issues • Develop contingency and recovery strategies and drive solutions through implementation • Build relationships with client project teams and act as a key point of contact • Support client satisfaction and operational excellence • Promote teamwork across a matrix environment, resolve conflicts, and maintain clear communication • Ensure team members are trained and follow study protocols, applicable SOPs, GCP, and local regulations • Drive improvements to enhance project efficiency and quality • Collaborate with global teams across multiple time zones • Travel approximately 10%

🎯 Requirements

• University or college degree, preferably in life sciences; certification in a related allied health profession; or equivalent combination of education and experience • At least five years of clinical pharmaceutical industry experience, including demonstrated competency in clinical project management • Alternatively, more than five years of supervisory experience in a healthcare setting combined with four years of clinical research experience in the pharmaceutical or CRO industries may be considered • Proven relevant clinical development experience and skills may be considered • Thorough knowledge of clinical project management processes • Ability to manage multiple competing priorities and resources effectively • Thorough knowledge of ICH Guidelines and GCP, including international regulatory requirements governing clinical development programs • Broad knowledge of the drug development process and client needs • Strong problem-solving, planning, organizational, and computer skills • Strong leadership and interpersonal skills • Ability to motivate matrix teams, work independently, resolve challenges, and negotiate professionally with clients • Valid current passport and driver's license • Ability to drive and undertake domestic and international travel, including overnight stays • Proficiency in English and French, both written and verbal

🏖️ Benefits

• Collaborative and inclusive work environment • Growth and career development opportunities • Opportunity to learn and grow • Remote work arrangement • Opportunity to contribute to life-changing clinical research • Global team collaboration

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