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Senior Director, Clinical Research, Metabolism

Merck
Boston, MA Full Time
POSTED ON 4/27/2025
AVAILABLE BEFORE 5/21/2025

Job Description

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity, and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement, and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

The Senior Director (Senior Principal Scientist) has primary responsibility for the planning and directing clinical research activities within the Atherosclerosis and Metabolism therapeutic area, with a particular focus on obesity and obesity-related metabolic disorders.

The Senior Director will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.

Specifically, the Senior Director may be responsible for :

  • Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug applications.
  • Developing clinical development strategies for investigational or marketed 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 drugs.
  • Analyzing and summarizing 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.

In executing these duties, the Senior Director may :

  • Supervise the activities of Clinical Scientists in the execution of clinical studies.
  • Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects.
  • Obtain internal and external expert opinion on scientific questions relevant to areas of responsibility.
  • The Senior Director is responsible for maintaining a strong scientific fund of knowledge by :

  • Maintaining awareness of scientific developments within one’s 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 particular fields of interest, particularly those who would be willing and able to assist in the evaluation of our company's drugs.
  • Attending appropriate scientific meetings to maintain one’s competency and awareness of research activities in areas of responsibility.
  • To accomplish these goals, the Senior Director may :

  • 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 20% of the time to manage future or ongoing clinical research projects.
  • Qualifications : Education

  • M.D or M.D. / Ph.D.
  • Required

  • Demonstrated record of scientific scholarship and achievement.
  • Experience in clinical medicine and background in biomedical research.
  • Strong interpersonal skills, as well as the ability to function in a team environment.
  • Preferred

  • Minimum of 3 years of clinical medicine experience.
  • Minimum of 3 years of industry experience in drug development or biomedical research experience in academia.
  • Board Certification in Endocrinology & Metabolism or Obesity Medicine.
  • Prior specific experience in clinical research and prior publication.
  • Current Employees apply HERE

    Current Contingent Workers apply HERE

    US and Puerto Rico Residents Only :

    Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

    We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics.

    U.S. Hybrid Work Model

    Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work model consisting of three total days on-site per week, Monday - Thursday, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.

    Expected US salary range : $268,500.00 - $422,700.00

    Available benefits include : bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days.

    Employee Status : Regular

    Relocation :

    Travel Requirements :

    Flexible Work Arrangements : Hybrid

    Job Posting End Date : 02 / 14 / 2025

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    Salary : $268,500 - $422,700

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