Oncology Clinical Strategy & Solutions Lead

Faro; New York (NY); On-site; USD 69,000 - 76,000; Full time

Benefits offered by this job

Retirement Plan (401k)

Job summary

Faro is seeking a seasoned Clinical Operations professional in the New York area to lead sponsor-driven pharmaceutical trials. You will interpret complex protocols, manage oncology studies, and collaborate across functions while leveraging EDС, IRT, CTMS and related technologies.

Candidates should have 5-7+ years of Clinical Operations experience, strong regulatory knowledge, and be open to travel. This contract role supports multiple sites and demands meticulous leadership and communication.

Qualifications

• Bachelor's degree required in physical or life or statistics.
• 5-7+ years of Clinical Operations work experience at a sponsor company in pharmaceutical clinical trials preferred. Experience as a Clinical Research Associate a plus.
• Strong knowledge of clinical trials and drug development processes
• Ability to read and comprehend complex clinical trial protocols and designs
• Oncology study experience
• Familiarity with and experience using clinical trial technologies (e.g., EDC, IRT, CTMS, ePRO, eCOA, eConsent, TMF)
• Knowledge of regulatory requirements and information governance frameworks (e.g. ICH, GCP, HIPAA, GDPR)
• Excellent team player with demonstrated track record of success in a cross-functional team environment; consistent commitment to delivering on team goals with a sense of shared urgency

Skills

Clinical Operations

Cross-functional teamwork

Regulatory knowledge

Protocol reading

Oncology study experience

Clinical trial technologies

Travel readiness

Education

Bachelor's degree in physical or life sciences or statistics

Tools

EDC

IRT

CTMS

ePRO

eCOA

eConsent

TMF

Job description

Faro is seeking a seasoned Clinical Operations professional in the New York area to lead sponsor-driven pharmaceutical trials. You will interpret complex protocols, manage oncology studies, and collaborate across functions while leveraging EDС, IRT, CTMS and related technologies.

Candidates should have 5-7+ years of Clinical Operations experience, strong regulatory knowledge, and be open to travel. This contract role supports multiple sites and demands meticulous leadership and communication.