Associate Project Manager – Oncology

🔥 6 minutes ago

🌐 Canada, United States – Remote

🇨🇦 Canada – Remote 🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👷‍♀️ 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

• Coordinate and manage clinical trials from start up through close out activities • Define and manage project resource needs and establish contingency plans for key resources • Ensure successful design, implementation, tracking and revision of project plans for assigned projects • Ensure project deliverables meet customer time, quality and cost expectations • Meet financial performance targets for assigned clinical projects • Serve as a key client contact for assigned projects • Collaborate with scientific and therapeutic leadership across project teams • Provide flexible, innovative, and proactive project solutions

🎯 Requirements

• Excellent oral and written communication skills • Ability to chair meetings and participate in bid defenses • Excellent planning and organizational skills with effective time management • Excellent interpersonal skills • Ability to work logically and methodically • Initiative and problem-solving skills • Ability to negotiate and liaise with clients in a professional manner • University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution • Minimum of three (3) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks • In lieu of the above requirements, candidates with > three (3) years supervisory experience in a health care setting and two (2) years clinical research experience in the pharmaceutical or CRO industries will be considered and/or proven ability and demonstration of relevant experience and skill in clinical development • Experience working with Oncology studies is required • Ability to travel when needed

🏖️ Benefits

• Equal employment opportunities 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