Senior Clinical Trial Manager - Gene Editing (Remote)

Arbor; United States; Remote; USD 165,000 - 185,000; Full time

Benefits offered by this job

Bonus eligibility

New hire equity

Parental leave 12 weeks

Health insurance subsidy 90% premiums

401(k) match

Transit/parking allowance

Discretionary time off

Job summary

Arbor Biotechnologies seeks an experienced Senior Clinical Trial Manager to lead day-to-day operations for early-phase gene-editing studies. You will manage sites, CROs, vendors, budgets, and trial timelines, partnering with internal teams to ensure smooth execution.

Reporting to the Senior Director of Clinical Operations, you will drive startup through close-out, oversee documentation, and ensure inspection readiness across trials conducted in the US and abroad. Remote-friendly role.

Qualifications

• Bachelor’s degree in a scientific, health-related, or related field.
• 6+ years of progressive clinical operations experience in pharma/biotech.
• Experience managing early-phase studies; rare disease or CNS preferred.
• Experience with US/global trials across CROs, vendors, labs, sites.
• Familiarity with regulatory submissions and GCP/ICH guidelines.

Responsibilities

• Lead day-to-day clinical trial operations across studies, sites, CROs, and vendors.
• Own study timelines, budgets, invoices, and vendor deliverables.
• Oversee TMF quality and inspection readiness documentation.
• Coordinate starter activities, site activation, monitoring, and close-out.
• Collaborate with cross-functional teams and investigator meetings.
• Manage clinical sample logistics and data-related activities.

Skills

Clinical operations leadership

Budget management

Vendor management

Study timelines

Cross-functional collaboration

Investigator meetings

Education

Bachelor’s degree in scientific/health field

Tools

Smartsheet

Microsoft Office

Job description

Arbor Biotechnologies seeks an experienced Senior Clinical Trial Manager to lead day-to-day operations for early-phase gene-editing studies. You will manage sites, CROs, vendors, budgets, and trial timelines, partnering with internal teams to ensure smooth execution.

Reporting to the Senior Director of Clinical Operations, you will drive startup through close-out, oversee documentation, and ensure inspection readiness across trials conducted in the US and abroad. Remote-friendly role.