Remote Hematology Oncology Clinical Director

Merck

Madison (WI)

Remote

USD 256,000 - 403,000

Full time

14 days+
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Benefits offered by this job

Remote work
Annual bonus
401(k) plan

Job summary

Merck is seeking a Clinical Director (MD or MD/PhD) to lead clinical research activities in Oncology, Hematology, across all development stages. The role includes study design, execution, regulatory reporting, and publication, with medical oversight and cross-functional collaboration.

The ideal candidate has 3+ years of clinical medicine experience and 1+ year in drug development or academic biomedical research, plus a proven publication record and excellent communication skills.

Qualifications

  • MD or MD/PhD required and Board Certified or Eligible in Oncology/Hematology preferred.
  • Minimum of 3 years of clinical medicine experience.
  • Minimum of 1 year of industry experience in drug development or biomedical research.
  • Demonstrated record of scientific scholarship and achievement.
  • Proven track record in clinical medicine and biomedical research.
  • Strong verbal and written communication and presentation skills.

Responsibilities

  • Plan and oversee clinical trials in oncology/hepatology? (note: keeping within evidence) design trials and operational plans.
  • Medical oversight and overall conduct of ongoing or new clinical trials for investigational or marketed drugs.
  • Analyze and summarize clinical findings to support safety, efficacy, and regulatory submissions.
  • Collaborate with cross-functional teams in regulatory affairs, statistics, manufacturing, and commercialization.
  • Travel as needed to manage future or ongoing clinical research projects.

Skills

Academic Presentations
Adaptability
Biomedical Research
Clinical Investigations
Clinical Judgment
Regulatory Requirements

Education

MD or MD/PhD

Job description

Merck is seeking a Clinical Director (MD or MD/PhD) to lead clinical research activities in Oncology, Hematology, across all development stages. The role includes study design, execution, regulatory reporting, and publication, with medical oversight and cross-functional collaboration.

The ideal candidate has 3+ years of clinical medicine experience and 1+ year in drug development or academic biomedical research, plus a proven publication record and excellent communication skills.

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