Global Clinical Programs Director & Execution Lead

MSD; Rahway (NJ); Sur place; USD 180 000 - 240 000; Plein temps

Résumé du poste

Merck & Co., Inc. in Rahway, NJ seeks an experienced Senior Program Lead to provide strategic and operational leadership across complex clinical development programs, spanning multiple disease areas.

You will direct global cross-functional teams, manage program plans and timelines, and drive risk mitigation and operational excellence across portfolios. The role emphasizes staff development, inspection readiness, regulatory submissions, and collaboration with stakeholders to deliver trials on

Qualifications

• Clinical Trials Monitoring, Cross-Functional Teamwork, Data Management, Ethical Standards, Exercises Judgment, Global Clinical Studies, Patient Safety, Regulatory Submissions, Scientific Writing, Therapeutic Knowledge

Responsabilités

• Lead global cross-functional teams in end-to-end clinical development.
• Develop and maintain the Clinical Operations Project Schedule with timelines for key milestones.
• Provide operational input on protocol design and program-level development planning documents.
• Provide program-level oversight to inform trial enrollment, site feasibility and engagement strategies.
• Conduct resource planning and staffing across a program or asset; manage Trial Managers.
• Oversee inspection readiness and collaboration with CQRM/CST to ensure quality and compliance.

Connaissances

Clinical Trials Monitoring

Cross-Functional Teamwork

Data Management

Ethical Standards

Exercises Judgment

Global Clinical Studies

Patient Safety

Regulatory Submissions

Scientific Writing

Therapeutic Knowledge

Formation

Bachelor’s degree + 15 years

Master’s + 12 years

PhD/PharmD + 8 years Pharmaceutical and/or clinical drug development experience

Description du poste

Merck & Co., Inc. in Rahway, NJ seeks an experienced Senior Program Lead to provide strategic and operational leadership across complex clinical development programs, spanning multiple disease areas.

You will direct global cross-functional teams, manage program plans and timelines, and drive risk mitigation and operational excellence across portfolios. The role emphasizes staff development, inspection readiness, regulatory submissions, and collaboration with stakeholders to deliver trials on