Immunology Study Lead for Global Clinical Trials

MSD Malaysia; Rahway (NJ); On-site; USD 117,000 - 184,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Medical, dental, vision

Job summary

Merck in Rahway, NJ seeks a Clinical Operations Lead to orchestrate the planning and execution of one or more clinical trials within the Tulisokibart program. The role requires expertise in study planning, country/site selection, and cross-functional collaboration to meet timelines and deliverables.

The ideal candidate demonstrates strong project management, leadership, and problem-solving skills, with solid knowledge of GCP/ICH regulatory requirements and excellent communication capabilities.

Qualifications

• Experience driving operational activities on clinical protocols.
• Solid knowledge of clinical research regulatory requirements (GCP/ICH).
• Ability to manage multiple priorities with planning and prioritization.
• Strong written and verbal communication skills.

Responsibilities

• Lead operational planning and execution of one or more clinical trials.
• Coordinate data management deliverables, timelines, and site selection.
• Collaborate with internal/external stakeholders to meet study objectives.
• Manage vendors and study partners to ensure milestones are met.
• Provide leadership in meetings and drive study goals in a matrix environment.

Skills

Clinical operations

Regulatory knowledge (GCP/ICH)

Project planning

Timeline management

Stakeholder management

Problem solving

Communication

Leadership

Team coordination

Microsoft Office

Education

Tools

MS Office

Job description

Merck in Rahway, NJ seeks a Clinical Operations Lead to orchestrate the planning and execution of one or more clinical trials within the Tulisokibart program. The role requires expertise in study planning, country/site selection, and cross-functional collaboration to meet timelines and deliverables.

The ideal candidate demonstrates strong project management, leadership, and problem-solving skills, with solid knowledge of GCP/ICH regulatory requirements and excellent communication capabilities.