Associate Director, Site Mgmt & Oversight Lead (remote)

csl.co.th

Base: $155,000 - $183,000; bonus/equity: incentive...
Fully remote
12 years clinical research experience
Site management and monitoring oversight
Cro vendor management and oversight
CSL Behring is seeking an Associate Director, Site Management & Oversight Lead for a fully remote position. The role involves overseeing clinical trials, ensuring compliance, and managing site relationships, with a focus on high-quality delivery within project timelines

Job Summary

  • This role leads one or more Therapeutic Areas to ensure all work is completed within project timelines with high quality while supporting remote operations due to travel needs.
  • The position requires building trusted relationships with investigators, serving as the primary sponsor contact, and advocating for process simplification to improve the site experience.
  • CSL Behring offers a competitive base salary range of $155,000 - $183,000 along with incentive compensation, equity, and a culture focused on inclusion and belonging.

Matching Summary

Match Score: 85

CSL Behring is seeking an Associate Director, Site Management & Oversight Lead for a fully remote position. The role involves overseeing clinical trials, ensuring compliance, and managing site relationships, with a focus on high-quality delivery within project timelines.

Salary

Base: $155,000 - $183,000; Bonus/Equity: Incentive compensation and equity included; Benefits: Not specified

Skills & Requirements

Must-have

  • 12 years clinical research experience
  • Site management and monitoring oversight
  • CRO vendor management and oversight
  • ICH guidelines and GCP knowledge
  • Team leadership and staff mentoring
  • Budget forecasting and management

Nice-to-have

  • Matrix environment navigation skills
  • Innovation in study approaches
  • Strong interpersonal conflict resolution
  • Drive to deliver program objectives
  • Ability to mentor reporting personnel

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Minimum 12 years relevant clinical research experience
  • Previous experience leading and managing professional staff
  • Solid understanding of drug development process steps
  • Experience overseeing large global clinical trials

Work Rights

Not specified

Tailored Resume

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