Senior Global Clinical Trial Leader (Hybrid)

U175 (FCRS = US175) Novartis Institutes for BioMedical Research, Inc.; Cambridge (MA); Hybrid; USD 126,000 - 234,000; Full time

Benefits offered by this job

Health insurance

401(k) with company match

Disability insurance

Paid time off

Job summary

Novartis Institutes for BioMedical Research, Inc. in Cambridge, MA seeks an experienced Clinical Scientist to lead complex early-phase trials from design through reporting, collaborating with physicians and scientists worldwide.

This hybrid role emphasizes patient-centric trial design and seamless execution across a global network. You will manage study design, protocols, data reviews, and cross-functional coordination, with 6+ years in clinical trials and an advanced life sciences background.

Qualifications

• Bachelor's degree in life sciences/healthcare required, 6+ years' experience in clinical trials development.
• Advanced degree in life sciences/healthcare preferred (PhD/MD/PharmD/Masters).
• Strong project management, planning, prioritization and organizational skills.

Responsibilities

• Operationally and scientifically lead complex clinical studies.
• Drive global clinical trial execution from design to final reporting.
• Lead matrix-managed global trial teams and collaborate with sites and providers.
• Develop study protocols and execution plans, ensuring quality standards.

Skills

Budget Management

Clinical Research

Clinical Trials

Coaching

Data Analysis

Data Integrity

Learning Design

Risk Monitoring

Education

Bachelor's degree in life sciences/healthcare

Advanced degree (PhD/MD/PharmD/Masters) preferred

Job description

Novartis Institutes for BioMedical Research, Inc. in Cambridge, MA seeks an experienced Clinical Scientist to lead complex early-phase trials from design through reporting, collaborating with physicians and scientists worldwide.

This hybrid role emphasizes patient-centric trial design and seamless execution across a global network. You will manage study design, protocols, data reviews, and cross-functional coordination, with 6+ years in clinical trials and an advanced life sciences background.