Associate Project Manager - Oncology (US/Canada)

Worldwide Clinical Trials • Quebec, QC

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About The Position

Worldwide Clinical Trials is a global, midsize Contract Research Organization (CRO) that focuses on pushing boundaries and innovating to find cures for persistent diseases. The company employs over 3,500 experts and aims to change the way the world experiences CROs. Their mission is to improve lives through passionate and purposeful work. They are committed to enabling professionals from all backgrounds to succeed by cultivating a diverse, inclusive, collaborative, and creative environment where people can thrive and do their best work. The Project Management team at Worldwide Clinical Trials combines operational rigor with therapeutic expertise and a client-focused approach. Global Project Leads (GPLs) and Clinical Project Managers (CPMs) guide project teams to deliver high-quality results with a focus on accuracy. The team collaborates across scientific and therapeutic leadership, coordinates project teams, and provides flexible, innovative, and proactive solutions. Professionals in this role are dedicated to a specific therapeutic area, allowing for in-depth global operational expertise and benefiting from the scientific and medical background of the company's experts.

Requirements

• University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
• Minimum of three (3) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks.
• Experience working with Oncology studies is required.
• Ability to travel when needed.

Nice To Haves

• 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.

Responsibilities

• Overall coordination and management of 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 that all project deliverables meet the customer’s time/quality/cost expectations.
• Meet financial performance targets for the assigned clinical projects.
• Serve as a key client contact for assigned projects.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level