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Senior Clinical Director, Clinical Research, Hematology

Job in Rahway, Union County, New Jersey, 07065, USA
Listing for: Dormont Manufacturing Co
Full Time position
Listed on 2026-07-04
Job specializations:
  • Research/Development
    Clinical Research, Medical Science
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 282200 - 444200 USD Yearly USD 282200.00 444200.00 YEAR
Job Description & How to Apply Below

Job Summary

Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in the Hematology Section. The company’s oncology medicines span all phases of clinical development (pre‑clinical to post‑licensure). The Senior Clinical Director may manage the entire cycle of clinical development for assigned studies, including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.

Responsibilities
  • Evaluating pre‑clinical and translational work to generate early clinical development plans and Investigational New Drug applications.
  • Developing clinical development strategies for investigational or marketed Hematology drugs.
  • Planning clinical trials (designing, collaborating on operational plans, etc.) based on the clinical development strategy.
  • Providing medical oversight and overall conduct of ongoing or new clinical trials for investigational or marketed drugs.
  • Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication.
  • Participating in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds.
  • Supporting business development assessments of external opportunities.
  • Actively engaging with other functional areas in support of study execution.
  • Working closely with a cross‑functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects.
  • Assisting the Executive Director and/or Associate Vice President in ensuring that appropriate personnel are informed of the progress of studies of our company and competitors’ drugs.
  • Providing expert opinion, internally and externally, on relevant scientific questions within their responsibility.
  • Maintaining awareness of scientific developments within the area of expertise, in terms of new scientific findings and research methodologies.
  • Identifying scientifically and operationally strong investigators who can assist in the development of our company’s investigational and marketed drugs.
  • Establishing communications with prominent clinical investigators in their field of interest, particularly those willing and able to assist in the evaluation of our company’s drugs.
  • Attending appropriate scientific meetings to maintain competency and awareness of research activities in the area of responsibility.
  • Authoring detailed development documents, presentations, budgets, and position papers for internal and external audiences.
  • Facilitating collaborations with external researchers around the world.
  • Traveling on company business about 20% of the time to manage future or ongoing clinical research projects.
Education

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

Required Experience and Skills

Must have experience in industry or as senior faculty in academia. Minimum of 3 years clinical medicine experience. Minimum of 3 years industry experience in drug development or biomedical research experience in academia. Demonstrated success in overseeing clinical studies and protocols, record of scientific scholarship, and achievement. Proven track record in clinical medicine and background in biomedical research. Strong interpersonal skills, ability to function in a team environment, outstanding verbal and written communication, and presentation skills.

Preferred Experience

Board Certified or eligible in Oncology, Hematology or related discipline. Prior specific experience in clinical research and prior publication.

Required Technical Skills
  • Clinical Development
  • Clinical Documentation
  • Clinical Judgment
  • Clinical Medicine
  • Clinical Reporting
  • Clinical Research Management
  • Clinical Trial Development
  • Clinical Trials
  • Data Analysis
  • Decision Making
  • Drug Development
  • Early Clinical Development
  • Ethical Standards
  • Hematology
  • Hemodialysis
  • Hemodynamic
  • Intellectual Curiosity
  • Interdisciplinary Problem Solving
  • Mentorship
  • Nephrology
  • Regulatory Affairs Compliance
  • Regulatory Compliance
  • Scientific…
Position Requirements
10+ Years work experience
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