Global Director Clinical Trial Programs & Studies

Merck & Co.; Rahway (NJ); Hybrid; USD 256,000 - 403,000; Full time

Benefits offered by this job

Health insurance

401(k) retirement plan

Hybrid work arrangements

Job summary

Merck & Co. is seeking a senior leader to oversee HQ-sponsored and outsourced trials across Therapeutic Areas, ensuring expert program execution from planning through delivery. You will partner with Clinical Development and GCTO stakeholders to drive execution, compliance, and continuous improvement in a highly cross-functional role.

You will lead a global team, manage resources, and champion AI-enabled modernization to optimize trial performance, risk mitigation, and regulatory readiness.

Qualifications

• Bachelor's degree required with concentration in a scientific discipline; advanced degree preferred.
• Extensive experience in planning and execution of clinical trials; ability to translate knowledge across organizational levels.
• Strong regulatory and quality knowledge including GCP/ICH and global requirements.

Responsibilities

• Translate TA objectives into executable operational strategies for clinical programs and studies.
• Own end-to-end delivery of the clinical program portfolio on time, within budget, and with high quality.
• Lead cross-functional collaborations and ensure readiness for inspections and audits.
• Develop and mentor a global team, manage resources, and drive continuous improvement.
• Drive modernization and AI-enabled solutions to enhance trial management and KPIs.

Skills

Artificial Intelligence

Clinical Development

Clinical Trial Planning

Clinical Trials

Digital Leadership

Executive Leadership

Global Team Collaboration

GCP

ICH GCP

KPI

Matrix Leadership

Ophthalmology

Regulatory Requirements

Strategic Leadership

Education

Bachelor's degree in a scientific field

Advanced scientific degree (MS/PhD/PharmD) preferred

Job description

Merck & Co. is seeking a senior leader to oversee HQ-sponsored and outsourced trials across Therapeutic Areas, ensuring expert program execution from planning through delivery. You will partner with Clinical Development and GCTO stakeholders to drive execution, compliance, and continuous improvement in a highly cross-functional role.

You will lead a global team, manage resources, and champion AI-enabled modernization to optimize trial performance, risk mitigation, and regulatory readiness.