Associate Director, Clinical Scientist — Immunology

MSD Malaysia

Rahway (NJ)

On-site

USD 142,000 - 224,000

Full time

4 days ago
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Job summary

Merck & Co., Inc. in Rahway, NJ, is seeking an Associate Director Clinical Scientist to provide scientific leadership across multiple studies and development programs, guiding study design, interpretation, and insights.

You will partner with Clinical Directors, Medical Monitors, Data Management, and Regulatory colleagues to ensure quality, strategy, and strong scientific integrity across indications. This role requires advanced biomedical training and 2+ years of clinical science experience.

Qualifications

  • Advanced degree and 2+ years of clinical science experience
  • Master’s degree with 6+ years of clinical science experience
  • Bachelor’s degree with 9+ years of clinical science experience
  • Experience with protocol development and clinical data review
  • Familiarity with autoimmune diseases and immunology

Responsibilities

  • Lead as the Clinical Scientist across multiple studies, from planning to reporting
  • Develop clinical protocols and informed consent forms for studies
  • Collaborate with cross-functional teams to align study objectives
  • Monitor safety signals and data quality through reviews
  • Translate evidence into development strategy and reports

Skills

Clinical Leadership
Clinical Data Review
Study Design
Data Management
Regulatory Compliance
Biostatistics
Strategic Thinking
Cross-functional Collaboration
Medical Monitoring
Safety Evaluation
Communication
Protocol Development

Education

Advanced degree in life sciences/medical field (PharmD/PhD/MD/DO/PA/ANRP)
Master’s degree in life sciences
Bachelor’s degree in life sciences

Job description

Merck & Co., Inc. in Rahway, NJ, is seeking an Associate Director Clinical Scientist to provide scientific leadership across multiple studies and development programs, guiding study design, interpretation, and insights.

You will partner with Clinical Directors, Medical Monitors, Data Management, and Regulatory colleagues to ensure quality, strategy, and strong scientific integrity across indications. This role requires advanced biomedical training and 2+ years of clinical science experience.

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