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Senior Clinical Project Manager

Job in Chicago, Cook County, Illinois, 60290, USA
Listing for: Cedent Consulting
Full Time position
Listed on 2026-09-25
Job specializations:
  • Healthcare
    Clinical Research
Job Description & How to Apply Below
Responsibilities Contribute to our cutting-edge radiopharmaceutical development program

Conceptualize, plan, design, place, execute, and summarize clinical trials

Drive daily vendor and site management, including collaboration with Study Medical Monitor and KOLs to determine the medical and scientific needs

Effectively communicate project-related information including the planning and execution of meetings and presentations as well as creation and maintenance of metrics, e.g., dashboards, timelines, resources, and budgets

Contribute to regulatory filings (e.g., IND / IMPD / CTN, NDA)
Identify issues and propose solutions. Proactively assess potential risks to the clinical study and propose mitigation plans

Work in an office (Wilmette, IL north of Chicago) with a dynamic, talented team

Qualifications MINIMUM EXPERIENCEBiotech or Pharma company clinical operations experience in progressively responsible positions, including Senior/Clinical Project or Trial Manager7+ years’ experience managing clinical trials including study design and initiation, oversight, study closeout, project management, and regulatory filings

Demonstrated ability to plan and execute Pharma-Sponsored clinical trials, managing vendors and resources in effective & creative manners to achieve business needs including on-time, on-budget, and on-spec study results for successful use in regulatory marketing applications

Thorough knowledge of ICH-GCP, Food and Drug Administration (FDA), and European regulations

Excellent communication (oral and/or written), leadership, and risk mitigation skills plus a positive attitude

Require minimal guidance; is able to function in an independent manner

Proven ability to effectively manage internal and external personnel in clinical trial conductPREFERRED EXPERIENCE9 years’ clinical trials experience in pharmaceutical or biotechnology firms

Experience in oncology trials

Experience managing clinical trials in Europe and/or Australia Experience in a small or growth-stage biopharma company
Position Requirements
10+ Years work experience
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