MSD

Senior Principal Scientist, Clinical Research, GI Oncology

MSD

full-time

Posted on:

Location Type: Hybrid

Location: Rahway • New Jersey • Pennsylvania • United States

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Salary

💰 $282,200 - $444,200 per year

Job Level

Senior

About the role

  • The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines.
  • The Senior Director will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.
  • Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug applications
  • Development of clinical development strategies for investigational or marketed Oncology drugs
  • Planning clinical trials (design, operational plans, settings) based on these clinical development strategies
  • Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Oncology 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 publications
  • Participation in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds.
  • Lead a cross-functional team including Clinical Scientists in endeavors ranging from drafting clinical study protocols to overseeing protocol adherence to assessing patient-level data, ensuring data completeness and integrity, and ultimately interpreting and contextualizing aggregate data to assess safety and efficacy
  • Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects
  • Assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and engage with internal and external experts on scientific questions relevant to their areas of responsibility.
  • Maintain a strong scientific fund of knowledge by maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies.
  • Identification of 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 particular field of interest, particularly those who will be willing and able to assist in the evaluation of our Company's drugs
  • Attend appropriate scientific meetings to maintain their competency and to maintain awareness of research activities in their area of responsibility.
  • Author detailed development documents, presentations, budgets, and position papers for internal and external audiences
  • Facilitate collaborations with external researchers around the world
  • Travel on company business about twenty (20) percent of the time to manage future or ongoing clinical research projects.

Requirements

  • Required M.D or M.D./Ph.D.
  • Minimum 3 years of clinical medicine experience in adult or pediatric oncology and/or hematology
  • Minimum 1 year of drug-development/pharmaceutical industry experience or biomedical research experience in academia/fellowship
  • Demonstrated record of scientific scholarship and achievement
  • Strong interpersonal and communication skills, as well as the ability to function in a large cross-functional team environment are essential.
  • Successful completion of an ACGME-medical oncology, combined medical oncology/hematology or pediatric hematology fellowship (Preferred)
  • Board Certified in adult or pediatric oncology (and/or hematology) (Preferred)
Benefits
  • medical, dental, vision healthcare and other insurance benefits (for employee and family)
  • retirement benefits, including 401(k)
  • paid holidays, vacation, and compassionate and sick days
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical researchstudy designregulatory reportingclinical trial monitoringdata analysisclinical study protocolsdrug developmentinvestigational new drug applicationsclinical findings analysisscientific scholarship
Soft Skills
interpersonal skillscommunication skillsteam collaborationleadershipstrategic planningproblem-solvingdata integrity assessmentscientific communicationproject managementcross-functional teamwork
Certifications
M.D.M.D./Ph.D.Board Certified in adult oncologyBoard Certified in pediatric oncologyBoard Certified in hematology