Remote Clinical Director, Hematology Oncology Trials

Merck; Trenton (NJ); Remote; USD 256,000 - 403,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401(k) Plan

Paid holidays

Vacation & Sick days

Job summary

Merck is seeking a Clinical Director (Principal Scientist) to lead clinical research in Oncology, Hematology. The role covers design, execution, monitoring, analysis, regulatory reporting, and publication across development stages.

It emphasizes medical oversight, collaboration with cross-functional teams, and travel to manage trials. Qualifications include MD or MD/PhD, 3+ years clinical medicine, and 1+ year in drug development or biomedical research, with strong communication skills and

Qualifications

• Minimum of 3 years of clinical medicine experience.
• Minimum of 1 year of industry experience in drug development or biomedical research.
• Demonstrated record of scholarly achievement.
• Strong interpersonal, teamwork, and communication skills.

Responsibilities

• Plan clinical trials and design operational plans.
• Medical oversight of ongoing or new trials for investigational or marketed drugs.
• Analyze findings to support safety, efficacy, and regulatory decisions.
• Collaborate with cross-functional teams in development, regulatory, statistics, and manufacturing.
• Travel ~20% of the time.

Skills

Academic Presentations

Adaptability

Allergy & 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

MD

MD/PhD

Job description

Merck is seeking a Clinical Director (Principal Scientist) to lead clinical research in Oncology, Hematology. The role covers design, execution, monitoring, analysis, regulatory reporting, and publication across development stages.

It emphasizes medical oversight, collaboration with cross-functional teams, and travel to manage trials. Qualifications include MD or MD/PhD, 3+ years clinical medicine, and 1+ year in drug development or biomedical research, with strong communication skills and