Current jobs related to Senior Principal Scientist, Clinical Research, GYN malignancies - RAHWAY NJ - Merck Sharp & Dohme (MSD)


  • Rahway, New Jersey, United States Merck Sharp & Dohme (MSD) Full time

    About the RoleAs a Senior Principal Scientist, Clinical Research, GYN Malignancies at Merck Sharp & Dohme (MSD), you will play a critical role in planning and directing clinical research activities involving new or marketed oncology medicines. Your primary responsibility will be to manage the entire cycle of clinical development, from study design and...


  • Rahway, United States Merck Sharp & Dohme (MSD) Full time

    Job DescriptionOur company in the United States and Canada, 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,...


  • RAHWAY, NJ, United States Merck Sharp & Dohme (MSD) Full time

    Job DescriptionOur 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,...


  • RAHWAY, NJ, United States Merck Sharp & Dohme (MSD) Full time

    Job DescriptionOur 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,...


  • RAHWAY, NJ, United States Merck Sharp & Dohme (MSD) Full time

    Job DescriptionOur company in the United States and Canada, 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,...


  • Rahway, United States Merck Sharp & Dohme (MSD) Full time

    Job DescriptionOur 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,...


  • Rahway, United States Merck Sharp & Dohme (MSD) Full time

    Job DescriptionOur company in the United States and Canada, 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,...


  • Rahway, United States Merck Sharp & Dohme (MSD) Full time

    Job DescriptionOur 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,...


  • Rahway, United States Merck Sharp & Dohme (MSD) Full time

    Job DescriptionOur company in the United States and Canada, 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,...


  • Rahway, United States MSD Malaysia Full time

    Senior Principal Scientist, Upstream Biologics Process R&DSenior Principal Scientist, Upstream Biologics Process R&DApply remote type Not Applicable locations USA - New Jersey - Rahway time type Full time posted on Posted 4 Days Ago time left to apply End Date: January 17, 2025 (27 days left to apply) job requisition id R327660Job DescriptionOur Scientists...


  • Rahway, New Jersey, United States Merck Sharp & Dohme (MSD) Full time

    Merck Sharp & Dohme (MSD) is seeking a Principal Scientist/Clinical Research Leader to join our team in Devices and Drug-Device Combinations CMC (Chemistry, Manufacturing & Controls).You will report to the Director of Device Regulatory Affairs for Autoinjector Development Programs and will be responsible for spearheading regulatory activities for Devices and...

  • Principal Scientist

    3 weeks ago


    Rahway, United States MSD Malaysia Full time

    Principal Scientist, Downstream Biologics Process R&DOur Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities, cutting-edge science, and technology, we partner to deliver the next medical breakthrough. We are seeking a collaborative, self-directed learner with a penchant for problem-solving and expertise in downstream...


  • RAHWAY, NJ, United States Merck Sharp & Dohme (MSD) Full time

    Job DescriptionOur 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,...


  • Rahway, New Jersey, United States Merck Sharp & Dohme Full time

    Job DescriptionThe Senior Principal Scientist has primary responsibility for planning and directing clinical research activities involving new or marketed Oncology medicines. This includes managing the entire cycle of clinical development, from study design and placement to monitoring, analysis, regulatory reporting, and publication.Key...


  • RAHWAY, NJ, United States Merck Sharp & Dohme (MSD) Full time

    Job DescriptionPosition Description:Senior Principal Scientist, Biostatistics (Hybrid)In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company’s renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies...


  • Rahway, New Jersey, United States Merck Sharp & Dohme Full time

    Job OverviewMerck Sharp & Dohme seeks a skilled Senior Principal Scientist, Biostatistics to lead statistical activities for clinical drug/vaccine projects. This role involves serving as a statistical lead in project teams, developing biostatistical support for related drug/vaccine projects, and interacting with Clinical, Regulatory, Statistical Programming,...


  • Rahway, New Jersey, United States Merck Sharp & Dohme Full time

    Clinical Development Lead, Cancer Medicines Job DescriptionThis role involves managing the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. The Senior Director may also supervise Clinical Scientists in the execution of clinical studies and work closely with cross-functional...


  • Rahway, New Jersey, United States Merck Sharp & Dohme (MSD) Full time

    Job OverviewA Senior Research Scientist, Analytical R&D Lead role is available at our Kenilworth, New Jersey research facility. We are seeking an experienced professional to lead analytical problem-solving efforts at the interface of biology, chemistry, and lab informatics disciplines. The successful candidate will be responsible for developing, qualifying,...


  • Rahway, New Jersey, United States Merck Sharp & Dohme Full time

    Job DescriptionThe Senior Principal Scientist is responsible for planning and directing clinical research activities involving new or marketed oncology medicines. This includes managing the entire cycle of clinical development, from study design and placement to monitoring, analysis, regulatory reporting, and publication. The Director will work closely with...


  • Rahway, New Jersey, United States Merck Sharp & Dohme Full time

    Job OverviewWe are seeking an experienced Senior Principal Scientist, Biostatistics to join our team in Merck Sharp & Dohme. The successful candidate will have a strong background in statistical analysis methodologies and experimental design.Key ResponsibilitiesLiaises with Clinical, Regulatory, Statistical Programming, Data Management, and Research...

Senior Principal Scientist, Clinical Research, GYN malignancies

1 week ago


RAHWAY NJ, United States Merck Sharp & Dohme (MSD) Full time

Job DescriptionOur 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 (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 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 plan and Investigational New Drug applications.Developing of clinical development strategies for investigational or marketed Oncology drugsPlanning clinical trials (design, operational plans, settings) based on these clinical development strategiesMonitoring 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; andParticipation 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, theThe Senior Director may:Supervise the activities of Clinical Scientists in the execution of clinical studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; andAssist the Senior 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 methodologiesIdentification of scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugsEstablishing 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's drugsAttending 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 audiencesFacilitating collaborations with external researchers around the worldTravel on company business about twenty (20) percent of the time to manage future or ongoing clinical research projects. QualificationsMinimum education required:• M.D or M.D./Ph.D.Required experience and skills:Must have experience in industry or senior faculty in academiaMinimum of 3 years of clinical medicine experienceMinimum of 1 year of industry experience in drug development or biomedical research experience in academiaExperience in gynecological malignancies preferred but not requiredDemonstrated record of scientific scholarship and achievementA proven track record in clinical medicine and background in biomedical research is essentialStrong interpersonal skills, as well as the ability to function in a team environment are essential.NOTICE FOR INTERNAL APPLICANTSIn accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.Preferred• Board Certified or Eligible in Oncology (and/or Hematology)• Prior specific experience in clinical research and prior publicationCurrent Employees apply HERECurrent Contingent Workers apply HEREUS 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.  For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:EEOC Know Your RightsEEOC GINA Supplement​Pay Transparency NondiscriminationWe are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State ActsU.S. Hybrid Work ModelEffective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.Expected US salary range:$268,500.00 - $422,700.00Available 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. A summary of benefits is listed here.San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance OrdinanceLos 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 OrdinanceSearch 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: RegularRelocation:InternationalVISA Sponsorship:YesTravel Requirements:25%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aJob Posting End Date:12/27/2024*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. SummaryLocation: USA - New Jersey - Rahway; USA - Pennsylvania - North Wales (Upper Gwynedd)Type: Full time