Snr Clinical Project Manager - Mood

198297
  • $150,000.00 to $180,000.00
  • Chapel Hill United States

 

Overview

Are you an experienced clinical project leader ready to make an impact in the field of mood disorders and neuropsychiatry? This is a fantastic opportunity to lead innovative global Phase III studies, working on cutting-edge therapeutics including Major Depressive Disorder (MDD), epilepsy, and potentially psychedelics. Join a dedicated team committed to advancing mental health treatments and gaining invaluable experience with a major life sciences organization. If you thrive in a fast-paced environment and want to grow your career in a mission-driven setting, this role offers a rewarding pathway.

About our client

Our client is a leading organization in the life sciences sector, focusing on developing pioneering therapies for neurological and psychiatric conditions. Their mission is to improve lives through innovative research and clinical development. With a global footprint, they support groundbreaking studies and aim to transform mental health care worldwide.

The opportunity (Role summary)

As a Senior Clinical Project Manager specializing in mood disorders, you will oversee and drive large-scale, complex clinical trials. You’ll work closely with cross-functional teams, including clinical, regulatory, and data management, to ensure project success from start-up through completion. This on-site role in the US allows for flexible work arrangements within a collaborative, dynamic environment.

Key responsibilities

  • Lead the planning, execution, and delivery of global Phase III clinical studies for mood disorder treatments.
  • Manage relationships with multiple stakeholders, including investigative sites, vendors, and internal teams.
  • Drive study timelines, budgets, and compliance to ensure seamless progress.
  • Partner with data teams and external partners to ensure high-quality data collection and reporting.
  • Ensure adherence to regulatory standards and company policies.
  • Oversee trial start-up activities, site management, and study conduct.
  • Contribute to study design, risk management, and troubleshooting.

What you’ll bring

  • Minimum of 5 years’ experience in clinical project management, with a strong background in neuroscience, mood disorders, or psychiatric conditions.
  • Extensive hands-on experience managing global Phase III studies in a CRO or pharmaceutical setting.
  • Experience with neuro-related indications such as MDD, epilepsy, or psychotic disorders.
  • Well-versed in ICH-GCP guidelines, clinical trial regulations, and study start-up processes.
  • Proven ability to hit deadlines, manage complex projects, and lead cross-functional teams.
  • Strong communication skills and the ability to adapt in a fast-paced environment.
  • Eligible to work on-site in the US.

Compensation & benefits

This role offers a competitive base salary ranging from £150,000 to £180,000 per year, complemented by performance-based bonuses. Exact compensation details will be shared during the interview process.

Call to action

If you're eager to contribute to groundbreaking mental health research and grow your career with a forward-thinking organization, apply now. Join a team dedicated to making a difference in patients’ lives.


Human review note:
Sometimes we use AI to draft job adverts using information from our CRM as part of our effort to work more efficiently so we can focus on what matters most: getting to know you. If you apply, a real person from our team will review your details and reach out. We’re committed to transparency, fairness, and human connection.

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Meet Life Sciences. Meet Life Sciences Ltd (No.06972871) a company registered in England and Wales at Irongate House, 22-30 Dukes Place, London, EC3A 7LP.
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