Global Clinical Trials Lead (Hybrid)

Alnylam Pharmaceuticals

Cambridge (MA)

Hybrid

USD 145,000 - 196,000

Full time

14 days+
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Benefits offered by this job

Bonus eligibility
Equity incentive
Medical insurance
Dental & Vision
401(k) match
Paid time off
Wellness days
Holiday entitlement
Recharge breaks

Job summary

Alnylam Pharmaceuticals seeks a Global Study Lead to orchestrate end-to-end global clinical trials from start-up to closeout. You will guide cross-functional teams, manage timelines and budgets, and ensure GCP and company procedures are followed.

Hybrid work options in Cambridge, MA or Philadelphia, PA with potential for remote arrangement for exceptional candidates. Responsibilities include trial delivery, vendor oversight, risk management, inspection readiness, and collaboration across

Qualifications

  • 7+ years of clinical research experience in CRO/biotech/pharma settings.
  • Experience leading global Phase 1-4 trials and Phase 3 registrational studies.
  • Proven ability to manage trial budgets, timelines and quality.

Responsibilities

  • Lead cross-functional trial teams to develop and execute study operational plans.
  • Accountable for trial delivery: timelines, budget, quality and milestones.
  • Oversee CRO/vendor selection, onboarding, contracting and monitoring.
  • Identify operational risks and implement mitigations across studies.
  • Ensure compliance with global regulations, GCP and internal SOPs.
  • Prepare for Health Authority inspections and internal QA audits.

Skills

Cross-functional leadership
Budget management
Regulatory compliance
Risk management
Vendor management
Project planning
Communication
MS Excel
MS Project

Education

BS/ BA degree

Tools

MS Project
MS Excel
CTMS

Job description

Alnylam Pharmaceuticals seeks a Global Study Lead to orchestrate end-to-end global clinical trials from start-up to closeout. You will guide cross-functional teams, manage timelines and budgets, and ensure GCP and company procedures are followed.

Hybrid work options in Cambridge, MA or Philadelphia, PA with potential for remote arrangement for exceptional candidates. Responsibilities include trial delivery, vendor oversight, risk management, inspection readiness, and collaboration across

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