VP, Clinical Operations – Global FIH Trial Leader

NewLimit

South San Francisco (CA)

On-site

USD 300,000 - 460,000

Full time

14 days+

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Benefits offered by this job

Health, dental, and vision insurance
401(k) with company match
Paid parental leave
20 days PTO + holidays
Meals and snacks on-site

Job summary

NewLimit is seeking a VP/Senior Director of Clinical Operations to orchestrate our first clinical trials focused on reprogramming medicines for aging. You will lead trial execution across protocols, CROs, and startup activities in US, AUS/NZ, EU, UK, with a patient-centric mindset.

As a founding member of the clinical operations team, you will manage timelines, budgets, and metrics, navigate regulatory requirements, and build a high-performance team to accelerate development and regulatory

Qualifications

  • 10+ years of industry experience in Clinical Operations.
  • Proven ability to orchestrate trials with CRO partners.
  • Recent experience managing first-in-human trials.
  • Experience spanning US, Australia, NZ, EU, UK, Japan.
  • Strong data-driven mindset with metrics and reporting.
  • Experience budgeting, forecasting and resource planning for trials.

Responsibilities

  • Lead clinical trial execution from protocol development to startup activities.
  • Manage CRO selection and oversight across geographies.
  • Ensure designs and execution maximize patient benefit and data value.
  • Own trial timelines and budgets; build operations metrics.
  • Address recruitment, cross-border logistics, regulatory compliance, staffing.
  • Build and lead the founding clinical operations team.
  • Support regulatory submissions and ongoing global compliance.

Skills

Clinical Operations
CRO Management
First-in-Human Trials
Global Trial Management
Metrics & Reporting
Budgeting & Forecasting

Education

Life sciences degree

Job description

NewLimit is seeking a VP/Senior Director of Clinical Operations to orchestrate our first clinical trials focused on reprogramming medicines for aging. You will lead trial execution across protocols, CROs, and startup activities in US, AUS/NZ, EU, UK, with a patient-centric mindset.

As a founding member of the clinical operations team, you will manage timelines, budgets, and metrics, navigate regulatory requirements, and build a high-performance team to accelerate development and regulatory

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