What are the responsibilities and job description for the Senior Manager, Global Site Management (Armonk, NY, Warren, NJ or Cambridge, MA) position at kps life?
KPS Life is hiring a Sr. Manager, Global Site Management to be fully dedicated to our sponsor client and work hybrid 3 days a week in either Warren, NJ or Armonk, NY.
This is a great opportunity for an experienced clinical operations professional to take a strategic role in global site management, risk-based monitoring, and CRO/FSP oversight. You’ll partner with clinical study teams and cross-functional stakeholders to strengthen monitoring strategies, drive vendor performance, identify operational risks, and support high-quality clinical trial delivery.
Interested in making an impact on global clinical trial delivery? Apply to KPS Life!
Senior Manager, Global Site Management
Position Overview
The Senior Manager, Global Site Management provides strategic oversight of monitoring and site management activities across a global clinical trial portfolio, ensuring quality, compliance, and consistent study execution. This role focuses on risk-based monitoring, CRO/FSP oversight, CRA resource planning, and site performance.
Key Responsibilities
This is a great opportunity for an experienced clinical operations professional to take a strategic role in global site management, risk-based monitoring, and CRO/FSP oversight. You’ll partner with clinical study teams and cross-functional stakeholders to strengthen monitoring strategies, drive vendor performance, identify operational risks, and support high-quality clinical trial delivery.
Interested in making an impact on global clinical trial delivery? Apply to KPS Life!
Senior Manager, Global Site Management
Position Overview
The Senior Manager, Global Site Management provides strategic oversight of monitoring and site management activities across a global clinical trial portfolio, ensuring quality, compliance, and consistent study execution. This role focuses on risk-based monitoring, CRO/FSP oversight, CRA resource planning, and site performance.
Key Responsibilities
- Monitoring Strategy & RBQM: Oversee monitoring strategies, risk-based quality management, risk indicators, and targeted source data verification (tSDV) specifications.
- CRO & FSP Oversight: Monitor CRO/FSP performance, CRA resource allocation, onboarding, training, and overall delivery.
- Study Delivery & Quality: Track site performance, identify and mitigate risks, support inspection readiness, and ensure compliance with ICH-GCP and applicable regulations.
- Cross-Functional Collaboration: Partner with Clinical Operations and other stakeholders to resolve issues, improve processes, and support study objectives.
- Performance & Process Improvement: Review metrics, identify trends, and implement improvements to monitoring effectiveness and trial execution.
- Budget & Resource Planning: Contribute to resource planning and budget oversight related to monitoring and site management activities.
- 4-year college degree required.
- At least 8 years of experience in the clinical trial industry, with experience in both monitoring and trial management.
- Strong knowledge of clinical monitoring, risk-based monitoring, and global clinical trial operations.
- Experience overseeing CROs, FSPs, and CRA performance.
- Knowledge of ICH-GCP, clinical research regulations, and inspection readiness requirements.
- Strong analytical, communication, and cross-functional collaboration skills.
- Ability to travel up to 25%.