Remote Senior Clinical Trial Manager - Gene Editing

Rippling, Inc.

Cambridge (MA)

Remote

USD 165,000 - 185,000

Full time

17 hours ago
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Benefits offered by this job

Bonus potential
Equity
Health benefits
Parental leave 12 weeks
Parking or transit
401(k) match

Job summary

Arbor Biotechnologies in Cambridge, MA is seeking a Senior Clinical Trial Manager to lead day-to-day operations for early-phase gene-editing studies, partnering with sites, CROs, vendors, and internal teams to drive start-up, execution, and close-out.

You will manage timelines, budgets, trial documentation, risk mitigation, and regulatory submissions, with hands-on leadership in a fast-paced startup environment and the option to work remotely. Travel domestically and internationally as needed.

Qualifications

  • Bachelor’s degree in a scientific, health-related, or related field.
  • ≥6 years of progressive clinical operations experience.
  • Experience managing early-phase studies; rare disease or CNS preferred.
  • Experience with US and global trials across CROs and vendors.
  • Knowledge of regulatory submissions and GCP/ICH guidelines.
  • Strong leadership, planning, and communication skills.

Responsibilities

  • Lead day-to-day clinical trial operations across studies, sites, CROs, vendors.
  • Manage start-up, site activation, monitoring, and close-out activities.
  • Own timelines, budgets, invoices, and vendor deliverables.
  • Oversee trial master file quality and documentation for inspections.
  • Review protocols, ICFs, CRFs, SAPs, CSRs, and study plans.
  • Partner with cross-functional teams to drive study execution and milestones.
  • Manage clinical sample logistics between patients, sites, and labs.
  • Coordinate safety review boards and data monitoring committees; data cuts.
  • Lead vendor review, onboarding, contracting, and oversight.
  • Build relationships with sites, CROs, vendors, and investigators; plan meetings.
  • Identify and resolve study risks and operational issues.
  • Represent the company externally with partners and sites.
  • Travel domestically and internationally as needed.

Skills

Clinical operations leadership
Vendor management
Budget management
Regulatory submissions
GCP/ICH knowledge
Cross-functional collaboration

Education

Bachelor's degree in a scientific field

Tools

Smartsheet
Microsoft Office

Job description

Arbor Biotechnologies in Cambridge, MA is seeking a Senior Clinical Trial Manager to lead day-to-day operations for early-phase gene-editing studies, partnering with sites, CROs, vendors, and internal teams to drive start-up, execution, and close-out.

You will manage timelines, budgets, trial documentation, risk mitigation, and regulatory submissions, with hands-on leadership in a fast-paced startup environment and the option to work remotely. Travel domestically and internationally as needed.

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