Senior Principal Scientist, Clinical Research, Gastrointestinal Oncology

Merck; Rahway (NJ); Hybrid; USD 180,000 - 240,000; Full time

Job summary

Merck & Co., Rahway, NJ, seeks a Senior Director/Sr. Principal Scientist in Oncology to lead planning and execution of clinical development for oncology medicines from pre-clinical to post-licensure.

You will design studies, monitor trials, and manage regulatory reporting and publication efforts, collaborating with regulatory, statistics, and manufacturing teams. The role requires MD or MD/PhD with 3+ years in clinical medicine and 3+ years in drug development or biomedical research, plus strong

Qualifications

• Must have experience in industry or senior faculty in academia.
• Minimum of 3 years of clinical medicine experience.
• Minimum of 3 year of industry experience in drug development or biomedical research in academia.
• Demonstrated record of scientific scholarship and achievement.
• A proven track record in clinical medicine and background in biomedical research is essential.
• Strong interpersonal skills and ability to work in a team environment.

Responsibilities

• Plan and direct clinical development activities for oncology medicines across phases.
• Develop clinical development strategies for investigational or marketed oncology drugs.
• Plan trials, monitoring, analysis, regulatory reporting and publication.
• Collaborate with cross-functional teams including regulatory affairs, statistics and manufacturing.
• Supervise Clinical Scientists in execution of studies.
• Travel to manage projects as needed (approximately 20%).

Skills

Cancer Research

Clinical Development

Clinical Trials

Cross-Functional Teamwork

Drug Development

Oncology Trials

Education

MD or MD/PhD

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 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.

Job Description

The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our Company's Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The 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 plan and Investigational New Drug applications;
• Developing 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 publication; and
• Participation 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

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; and
• Assist the Senior/Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.

The Senior Director is responsible for maintaining a strong scientific fund of knowledge by:

• Maintaining awareness of scientific developments within his/her 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 his/her particular field of interest, particularly those who will be willing and able to assist in the evaluation of our Company drugs.
• Attending appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility.

To Accomplish These Goals, The Senior Director May:

• Author detailed development documents, presentations, budgets, and position papers for internal and external audiences.
• Facilitating 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.

Qualifications

Education

• M.D or M.D./Ph.D.

Required

• Must have experience in industry or senior faculty in academia.
• Minimum of 3 years of clinical medicine experience.
• Minimum of 3 year of industry experience in drug development or biomedical research experience in academia.
• Demonstrated record of scientific scholarship and achievement.
• A proven track record in clinical medicine and background in biomedical research is essential.
• Strong interpersonal skills, as well as the ability to function in a team environment are essential.
• Outstanding verbal and written communication and presentation skills.

Preferred

• Board Certified or Eligible in Oncology.
• Prior specific experience in clinical research and prior publication.

Required Skills

Cancer Research, Clinical Development, Clinical Trials, Cross-Functional Teamwork, Drug Development, Oncology Trials.

Required Skills

Cancer Research, Clinical Development, Clinical Research, Clinical Trials, Clinical Trial Support, Drug Development, Oncology Trials

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.

As An Equal Employment Opportunity Employer, We Provide Equal Opportunities To All Employees And Applicants For Employment And Prohibit Discrimination On The Basis Of Race, Color, Age, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Protected Veteran Status, Disability Status, Or Other Applicable Legally Protected Characteristics. As a Federal Contractor, We Comply With All Aff... (truncated) ...

Additional location(s)

Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.

Additional location(s) Compensation Information

San Francisco Residents Only

We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only

We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status

Regular

Relocation

Domestic

VISA Sponsorship

Yes

Travel Requirements

25%

Flexible Work Arrangements

Hybrid

Shift

Not Indicated

Valid Driving License

No

Hazardous Material(s)

n/a

Job Posting End Date

10/15/2026

• A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID

R422055