Oncology Clinical Trial Lead: Global Site & Compliance

Mass Digital Health; Boston (MA); On-site; USD 68,000 - 233,000; Full time

Job summary

IQVIA in the United States seeks a Senior Trial Manager with 3–5+ years of country-level trial leadership and oncology experience. You will drive feasibility, recruitment planning, CAPAs, and budget management across complex studies, while ensuring regulatory compliance and data quality.

Binched with strong communication in English, you will collaborate with cross-functional teams and may travel as required to trial sites and investigator meetings.

Qualifications

• 3 to 5+ years of trial management experience, including independent management of complex clinical trials at country level.
• Oncology experience.
• Strong knowledge of ICH-GCP, Sponsor SOPs, local laws and regulations, and related protocol procedures.
• Willingness to travel as needed.
• Proficiency in speaking and writing the country language and English.

Responsibilities

• Leads country-level operational planning and execution for complex studies requiring advanced trial management expertise.
• Manages site feasibility, country-level recruitment strategies, and CAPA when issues arise.
• Maintains trial management systems, tracks progress, and communicates risks and mitigation plans.
• Oversees budgeting, finance reporting, and potential contract/budget negotiations.
• Ensures regulatory approvals (IEC/HA) and conducts training for local trial management teams.
• Acts as primary Sponsor contact at country level and coordinates investigator meetings when needed.

Skills

Trial management

Oncology experience

ICH-GCP knowledge

IT skills

Travel willingness

English proficiency

Education

BA/BS degree

Health/science degree

Job description

IQVIA in the United States seeks a Senior Trial Manager with 3–5+ years of country-level trial leadership and oncology experience. You will drive feasibility, recruitment planning, CAPAs, and budget management across complex studies, while ensuring regulatory compliance and data quality.

Binched with strong communication in English, you will collaborate with cross-functional teams and may travel as required to trial sites and investigator meetings.