Senior Clinical Project Manager (Chicago, IL)

Senior Clinical Project Manager (Chicago, IL)

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 EXPERIENCE

• Biotech or Pharma company clinical operations experience in progressively responsible positions, including Senior/Clinical Project or Trial Manager
• 7+ 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 conduct

PREFERRED EXPERIENCE

• 9 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

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