Global Clinical Program Lead - Late Respiratory & Immunology

AstraZeneca; Cambridge (MA); On-site; USD 288,000 - 432,000; Full time

Benefits offered by this job

Short-term incentive

Equity-based LTIP

401(k) plan

Paid vacation and holidays

Paid leaves

Health benefits including medical, Rx,

Job summary

AstraZeneca plc in Cambridge, MA is seeking a Global Clinical Program Lead to shape late-stage Respiratory development. You will lead a global team, drive study design, data interpretation and regulatory strategy, and collaborate across international functions to deliver safe, effective therapies for patients.

You will oversee a portfolio of studies, mentor study physicians and scientists, and ensure high ethical and scientific standards in line with GCP and global regulations.

Qualifications

• MD/PhD or equivalent medical or scientific qualification.
• 5–8 years of relevant clinical development experience with study design and trial execution.
• Experience working cross-functionally with regulatory, biostatistics and medical affairs.
• Strong English written and verbal communication; stakeholder engagement skills.

Responsibilities

• Lead and supervise Global Development Medical Directors and study teams.
• Oversee study design, monitoring, data interpretation and safety reviews.
• Develop risk mitigation strategies and liaise with regulatory agencies.
• Drive publication strategy and support cross-functional product teams.
• Mentor junior team members and ensure adherence to GCP and regulatory standards.

Skills

MD/PhD

Clinical development

Cross-functional teams

Biostatistics

Regulatory knowledge

GCP experience

English communication

Stakeholder engagement

Education

MD/PhD or equivalent

Job description

AstraZeneca plc in Cambridge, MA is seeking a Global Clinical Program Lead to shape late-stage Respiratory development. You will lead a global team, drive study design, data interpretation and regulatory strategy, and collaborate across international functions to deliver safe, effective therapies for patients.

You will oversee a portfolio of studies, mentor study physicians and scientists, and ensure high ethical and scientific standards in line with GCP and global regulations.