Senior Project Manager, Oncology Studies
Location: Philadelphia, PA — Hybrid (Wednesdays onsite)
Drive complex oncology clinical trials from strategy through completion for my client, ensuring studies stay on schedule, within budget, and focused on quality and patient safety. You’ll unite cross-functional teams, sponsors, sites, and clinical partners to successfully execute high-impact registration trials.
Why You Should Apply
Lead important, multisite oncology clinical trials
High-visibility role partnering directly with sponsors and senior leadership
Mentor and develop PMs, Associate PMs, and CRAs
Hybrid working environment
What You’ll Be Doing
Lead project plans, timelines, budgets, and sponsor communications
Coordinate Medical, Data Management, Regulatory, Monitoring, and Clinical Supplies teams
Ensure regulatory, protocol, SOP, data-quality, and safety compliance
Drive study issue and query resolution
Provide study status reporting and support new contract proposals
About You
Bachelor’s degree required; relevant Master’s degree and SOCRA certification preferred
Oncology clinical trial management and/or data management expertise
Pharmaceutical, CRO, site network, and multisite trial experience
Registration trial experience
Mastery of Excel and proficiency with Microsoft Office
How To Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to tomt@scientificsearch.com and tell me why you’re interested. Or, feel free to email your resume. Please include Job#20113.
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