Remote Hematology Clinical Trials Director

Merck

Carson City (NV)

Remote

USD 280,000 - 379,000

Full time

11 days ago
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Benefits offered by this job

Annual bonus
Long-term incentive
Comprehensive benefits

Job summary

Merck is seeking a Clinical Director (Principal Scientist) in Oncology/Hematology to lead planning and execution of clinical research across phases, from design to publication. The role emphasizes medical oversight, data interpretation, and cross-functional teamwork with regulatory, statistics, and manufacturing groups.

The position requires an MD or MD/PhD with a strong track record in clinical medicine and biomedical research, plus experience in drug development.

Qualifications

  • MD or MD/PhD degree required.
  • Minimum of 3 years clinical medicine experience.
  • Minimum of 1 year industry or academia drug development.
  • Proven record of scientific scholarship and publication.

Responsibilities

  • Plan clinical trials and collaborate on operational plans.
  • Provide medical oversight of ongoing or new trials for investigational or marketed drugs.
  • Analyze and summarize clinical findings to support safety, efficacy, and regulatory decisions.
  • Collaborate with internal/external teams for development of new compounds and further study of marketed drugs.
  • Support business development assessments of external opportunities.
  • Travel on company business about 20% of the time to manage projects.

Skills

Academic Presentations
Adaptability
Allergy and Immunology
Biomedical Research
Clinical Investigations
Clinical Judgment
Clinical Research
Clinical Trial Planning
Clinical Trial Support
Cross-Functional Teamwork
Ethical Standards
Intellectual Curiosity
New Technology Integration
Regulatory Requirements
Scientific Consulting

Education

M.D. or M.D./Ph.D.

Job description

Merck is seeking a Clinical Director (Principal Scientist) in Oncology/Hematology to lead planning and execution of clinical research across phases, from design to publication. The role emphasizes medical oversight, data interpretation, and cross-functional teamwork with regulatory, statistics, and manufacturing groups.

The position requires an MD or MD/PhD with a strong track record in clinical medicine and biomedical research, plus experience in drug development.

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