Site Activation Lead — Drive Clinical Startups & Outcomes

Premier Research International

United States

On-site

USD 104,000 - 128,000

Full time

4 days ago
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Benefits offered by this job

Health insurance
Retirement plans
Paid time off

Job summary

Premier Research is seeking a Clinical Lead - Site Activation Lead to join our Clinical Management team. You will coordinate with functional leads to deliver site activation and oversee start-up activities, ensuring alignment with timelines and contractual obligations.

The role requires leadership across functions, strong project budgeting skills, and a focus on data quality and timely communications. Ideal candidates have 5 years of related experience, familiarity with ICH/GCP regulations, and

Qualifications

  • 5 years professional experience in CL/RSM/PM or equivalent.
  • Strong leadership of study start-up teams.
  • Understanding of project budgets and timelines.
  • Excellent communication and collaboration skills.
  • Familiarity with ICH/GCP regulations.

Responsibilities

  • Coordinate with functional leads to deliver site activation.
  • Lead Site ID Kick Off meetings and review budgets.
  • Oversee SSU and activation deliveries per timeline.
  • Work with cross-functional teams to finalize country mix and site selection.
  • Escalate risks, develop mitigation, and communicate with sponsors.
  • Monitor CTMS data entry and provide delay rationales.
  • Provide weekly updates to team and client.

Skills

Leadership
Project management
Budget management
ICH/GCP knowledge
Interpersonal skills
Team collaboration

Education

Bachelor's degree in clinical or life sciences

Job description

Premier Research is seeking a Clinical Lead - Site Activation Lead to join our Clinical Management team. You will coordinate with functional leads to deliver site activation and oversee start-up activities, ensuring alignment with timelines and contractual obligations.

The role requires leadership across functions, strong project budgeting skills, and a focus on data quality and timely communications. Ideal candidates have 5 years of related experience, familiarity with ICH/GCP regulations, and

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