Job Description

Location: Malvern, PA (Hybrid - 2 days/week onsite)

We are partnering with an innovative late-clinical-stage CNS company focused on developing treatments for Alzheimer’s and Parkinson’s disease. This small, dynamic team is set to launch several key clinical trials in 2024, including:

• Ph3 Alzheimer’s Trial (100 sites in the US)
• Open-Label Alzheimer’s & Parkinson’s Study
• Ph3 Parkinson’s Trial

Key Responsibilities:

• Manage and execute clinical trial timelines and budgets, utilizing tools like Gantt charts.
• Collaborate closely with cross-functional teams to ensure smooth study progress.
• Oversee site monitoring and operational aspects.
• Proactively address challenges in a fast-paced, startup-like environment.
• Support multiple ongoing projects and initiatives.

MUST-HAVE Qualifications:

• Proven experience as a Clinical Project Manager, capable of working independently with minimal training.
• Experience with CNS clinical trials (Alzheimer’s preferred; Parkinson’s a plus).
• Strong background in managing timelines, financial planning, and using Gantt charts.
• Comfortable in a hybrid work model, with mandatory on-site presence in Malvern, PA, 2 days/week.
• Confident, dynamic personality capable of thriving in a startup environment.

Preferred Qualifications:

• Past experience as a CRA (Clinical Research Associate) is highly desirable.
• Strong leadership skills, with the ability to engage in healthy debates and voice opinions effectively.
• No strict educational requirements; extensive clinical research experience valued over formal degrees.

Benefits: Comprehensive package including medical, dental, vision, 401(k) with 4-4.5% match, PTO (3 weeks + rollover), and more.

Interview Process:

• Initial screening with the Director of Clinical Operations.
• On-site interview, including a case study.

If you're passionate about clinical research and looking for an exciting opportunity to join a growing company, we encourage you to apply!

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