Clinical Project Manager, CNS

Piper Companies

United States

Remote

USD 150,000 - 200,000

Full time

3 days ago
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Benefits offered by this job

Health, Vision, Dental
PTO & Holidays

Job summary

Piper Companies is seeking a Clinical Project Manager, CNS to lead CNS-focused clinical programs across Phase I-IV trials in multiple sites. You will oversee study timelines, budgets, vendor relationships, and cross-functional teams to drive successful CNS development programs.

Ideal candidates bring 8+ years in clinical research or project management within pharma/CRO sectors, with strong GCP/ICH knowledge and experience managing CROs and trial operations.

Qualifications

  • 8+ years of clinical research or clinical project management experience.
  • Extensive CNS clinical trials experience in neurology, psychiatry, or related areas.
  • Strong knowledge of GCP, ICH guidelines, FDA regulations, and trial processes.

Responsibilities

  • Lead planning, execution, and oversight of Phase I-IV CNS trials across multiple sites.
  • Manage study timelines, budgets, resources, and CRO/vendor relationships.
  • Collaborate with clinical operations, regulatory affairs, data management, biostatistics and medical affairs.
  • Monitor progress, identify risks, and implement mitigation strategies.

Skills

CNS clinical trials
Cross-functional leadership
Budget management
Vendor management
Regulatory knowledge

Education

Bachelor's degree in Life Sciences or related field
Advanced degree preferred

Tools

CTMS
EDC platforms

Job description

Piper Companies is seeking a Clinical Project Manager, CNS to lead and oversee clinical research programs focused on central nervous system (CNS) therapeutic areas for a leading organization within the pharmaceutical and biotechnology industry. The Clinical Project Manager, CNS will be responsible for managing clinical trial operations, ensuring study milestones are achieved, and coordinating cross-functional teams to support successful clinical development initiatives.

Responsibilities of the Clinical Project Manager, CNS:
  • Lead the planning, execution, and oversight of Phase I-IV CNS clinical trials across multiple sites.
  • Manage study timelines, budgets, resources, and vendor relationships to ensure project success.
  • Collaborate with clinical operations, regulatory affairs, data management, biostatistics, and medical affairs teams.
  • Monitor study progress, identify risks, and implement mitigation strategies to maintain project timelines.
  • Ensure compliance with ICH-GCP guidelines, FDA regulations, and applicable industry standards.
  • Oversee CRO activities and provide leadership during study start-up, enrollment, monitoring, and closeout activities.
  • Prepare and present project updates, metrics, and status reports to key stakeholders and executive leadership.
  • Support inspection readiness and contribute to audit preparation activities.
Requirements of the Clinical Project Manager, CNS:
  • 8+ years of clinical research or clinical project management experience within the pharmaceutical, biotechnology, or CRO industry.
  • Extensive experience managing CNS clinical trials, including neurology, psychiatry, or related therapeutic areas.
  • Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical trial processes.
  • Proven experience managing CROs, vendors, and cross-functional clinical teams.
  • Demonstrated ability to manage complex clinical programs, budgets, and timelines simultaneously.
  • Excellent communication, organizational, and stakeholder management skills.
  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; advanced degree preferred.
  • Experience with CTMS, EDC platforms, and clinical trial management tools.
Compensation for the Clinical Project Manager, CNS:
  • Salary range: $150,000 - $200,000 base salary
  • Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.
Keywords:

Clinical Project Manager, CNS, Central Nervous System, Clinical Trials, Clinical Operations, Pharmaceutical Industry, Biotechnology, CRO Management, Neurology, Psychiatry, Clinical Research, Project Management, ICH-GCP, FDA Regulations, Phase I, Phase II, Phase III, Phase IV, Vendor Management, CTMS, EDC, Risk Management, Study Start-Up, Clinical Development, Site Management, Regulatory Compliance, Cross-Functional Leadership, Clinical Program Management

This job opens for applications on 10/16/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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