Senior Principal Scientist, Clinical Research, Immunology
$282.2kMerck Sharp & Dohme (MSD)
Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director May Be Responsible For:• Evaluating pre-clinical and translational work for the purpose of generating the early clinical development plan and Investigational New Drug applications.• Providing clinical development support of business development assessments of external opportunities to grow the Immunology Pipeline• Developing clinical development strategies for investigational drugs and 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 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 compoundsThe 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 Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our company 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 drugs in Immunology.• Establishing collaborative relationships with external experts in Rheumatology, Gastroenterology, Dermatology, and pulmonary disease, particularly those whose research focus and expertise can inform and assist the evaluation of the company's investigational 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.• 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.QualificationsEducation minimum required:M.D., D.O., M.D./PhD, or D.O./PhD.Required experience and skills:• Experience in the design and/or execution of phase 2 or 3 clinical trials specifically in Immunology (Rheumatology, Gastroenterology or Dermatology)• Minimum of 3 years of clinical medicine experience• Minimum of 5 years of industry experience in drug development• Demonstrated record of scientific scholarship and achievement• Strong interpersonal skills, as well as the ability to work collaboratively in a cross-functional team environment.Required Skills: Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies, Clinical Trial Development, Clinical Trials, Dermatology, Drug Development, Gastroenterology, Inflammatory Bowel Diseases, Pharmaceutical Industry, Regulatory Compliance, RheumatologyPreferred Skills: Current 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.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 affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:EEOC Know Your RightsEEOC GINA SupplementWe are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills 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 ActsThe salary range for this role is$282,200.00 - $444,200.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.We offer a comprehensive package of benefits. Available benefits include 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. More information about benefits is available at .You can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.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:DomesticVISA Sponsorship:NoTravel Requirements:10%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aJob Posting End Date:08/20/2026*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. SummaryLocation: USA - New Jersey - Rahway; USA - Pennsylvania - North Wales (Upper Gwynedd)Type: Full time
$145.47k - $176.27k
...efficacy of life‑saving medicines administered to patients in clinical studies. Our team is involved at the earliest stages of... ...successful commercial launch. Position Summary The Senior Principal Scientist will serve as a CMC Analytical Lead (CMC‑AL) for drug candidates...PrincipalSeniorHourly payFull timeTemporary workPart timeSummer workLive inRemote workFlexible hoursShift work$117k - $184.2k
Job DescriptionThe Early Clinical Scientist (ECS) coordinates the design, planning and execution... ...or study manager role in clinical research at a pharmaceutical or biotech company... ...experience a plus. Experience managing Immunology and/or vaccine trials with an ability...SeniorFull timeFor contractorsLocal areaWorldwideFlexible hours$190.8k - $300.3k
...regulatory challenges with rigor and professionalism.The Senior Principal Scientist, Regulatory Affairs Liaison is responsible for the development... ...within and external to Global Regulatory Affairs and Clinical Safety (GRACS) on regulatory issues as they arise with the...PrincipalSeniorFull timeFor contractorsLocal areaWorldwideFlexible hours$190.8k - $300.3k
...BARDS (Biostatistics and Research Decision Sciences), a... ..., quantitative scientists, in partnership with other... ...This position is for a principal scientist in biostatistics... ...; and with good clinical trial experience in Phase... ...with respiratory and immunology disease areas are desired...PrincipalFull timeFor contractorsWork experience placementLocal areaWorldwideFlexible hours$156.9k - $247k
...DescriptionThe Biologics Analytical Research & Development department of... ...is seeking applicants for a Principal Scientist position available at its... ...visible and impactful senior scientific role tasked with... ...stability assays for testing of clinical trial material and in...PrincipalFull timeFor contractorsLocal areaFlexible hours$173.2k - $272.6k
...DescriptionIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department... ...and Development division, quantitative scientists, in partnership with other subject... ...Statistical Programming, Data Management, Clinical Research, Regulatory, Observational Research...PrincipalFull timeFor contractorsLocal areaFlexible hours$156.9k - $247k
Job DescriptionPrincipal Scientist, Pharmaceutical Analytical Sciences The Pharmaceutical... ...company has an exciting opportunity for a Principal Scientist based in Rahway, NJ. Join us... ...towards regulatory submissions to enable clinical trials. Your main responsibilities, in not...PrincipalFull timeFor contractorsLocal areaWorldwideFlexible hours$173.2k - $272.6k
Job DescriptionThe Biologics Process Research & Development organization within our Research... ...with colleagues in Discovery, Pre-clinical and Early Development to rapidly... ...experienced individual to join our team as a Principal Scientist. In this role, the successful...PrincipalFull timeFor contractorsLocal areaFlexible hours$173.2k - $272.6k
...Programming is in the Biostatistics and Research Decision Sciences (BARDS) department at... ...and the Biostatistics organization. The principal statistical programmer will partner with... ...external stakeholders including Statistics, Clinical Research, Data Management, Regulatory,...PrincipalFull timeFor contractorsLocal areaWorldwideFlexible hours$173.2k - $272.6k
...DescriptionBPR&D within our Company's Research Laboratories is on a mission... ...in Discovery, Pre-clinical, Early Development, Analytical... ...to influence the field.As a Principal Scientist you will have the... ...strategic initiatives; partner with senior leaders to set overall project...PrincipalFull timeFor contractorsLocal areaFlexible hours$173.2k - $272.6k
...Responsibilities:In the Development Sciences and Clinical Supply (DSCS) organization, we believe digital is... ...together to build technologies that truly impact how our scientists conduct research. We’re looking for a Principal Scientist to help realize this vision.In this role...PrincipalFull timeFor contractorsLocal areaVisa sponsorshipFlexible hours$117k - $184.2k
...DescriptionIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department... ...and Development division, quantitative scientists, in partnership with other subject... ...Development Statistics. Interacts with Clinical, Regulatory, Statistical Programming, Data...SeniorFull timeFor contractorsLocal areaFlexible hours$144.37k - $224.1k
Job DescriptionAssociate Principal Scientist, Statistical Programming - Rahway, NJ:Provide high quality statistical programming analysis and... ...opportunities arise.Programmatically synthesize preclinical / clinical data into analysis ready structures from varied data sources...PrincipalFull timeFor contractorsLocal area$173.2k - $272.6k
...development through commercialization. This principal scientist‑level role focuses on LAI formulation... ...systems, manufacturability, and clinical use considerations throughout development... ...and scientific leadership skills at the senior/principal level. Preferred Experience and...PrincipalFor contractors$142.4k - $224.1k
Job DescriptionThe Biologics Process Research & Development organization within our Research... ...with colleagues in Discovery, Pre-clinical and Early Development to rapidly... ...individual to join our team as an Associate Principal Scientist. In this role, a successful candidate...PrincipalFull timeFor contractorsLocal areaFlexible hours$117k - $184.2k
Job DescriptionThe Chemical Engineering Research & Development department (CERD), part of the Process Research and Development organization... ...deliver desired solid-state properties, purity, and yield for clinical programs across our different pipeline. This role involves the...SeniorFull timeFor contractorsWork experience placementLocal areaFlexible hours$173.2k - $272.6k
Job DescriptionThe Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory... ...on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.Develops worldwide product...PrincipalFull timeFor contractorsLocal areaWorldwideFlexible hours$142.4k - $224.1k
Job DescriptionAssociate Principal Scientist, Process ChemistryThe Process Chemistry... ...routes suitable for clinical and commercial supply.Drive... ...strategies and project outcomes to senior leadership and external... ...excellence and significant research accomplishments in synthetic...PrincipalFull timeFor contractorsLocal areaFlexible hours$117k - $184.2k
Job DescriptionWe are seeking a highly motivated and experienced Senior Scientist to join the Analytical Supply Analytical Sciences - API Supply group. This dynamic, laboratory-based position offers the opportunity to work in a fast-paced, multidisciplinary team, focused...SeniorFull timeFor contractorsLocal areaFlexible hours$173.2k - $272.6k
Job Description The Biologics Process Research & Development organization within our... ...closely with colleagues in Discovery, Pre-clinical and Early Development to rapidly... ...experienced individual to join our team as a Principal Scientist. In this role, the successful...PrincipalFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$310.9k
Job DescriptionOur Clinical Development teams manage studies to provide... ...standards. The Distinguished Scientist (Executive Director) and... ...planning and directing clinical research activities involving new or... ...may: Manage Directors and/or Senior Directors responsible for Oncology...Full timeFor contractorsLocal areaFlexible hours$156.9k - $247k
...Value and Implementation (V&I), Outcomes Research Oncology organization, which is... ...health outcomes. Under the guidance of senior leaders, this individual will support the... ...internal teams, and provide input into clinical, payer/access, marketing and value evidence...PrincipalFull timeFor contractorsLocal areaWorldwideFlexible hours$156.9k - $247k
Job DescriptionPrincipal Scientist - Device Technical and Engineering... ...support and influence clinical and commercial combination product... ...product development and launches.Principal ResponsibilitiesLead and set... ...and present ideas to senior leadershipExcellent communication...PrincipalFull timeFor contractorsLocal areaWorldwide- Job Description: The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing. Responsibilities: Review...PrincipalSenior
$109k - $174.8k
...Innovative Medicine is recruiting for a Senior Scientist, AI Applications, R&D Oncology to join... ...knowledge. Your work will directly accelerate research across the drug development pipeline,... ...discovery, translational research and clinical trials—making reasoning agents faster,...SeniorFull timeTemporary workLocal areaRemote work$310.9k
...DescriptionThe Executive Director (Distinguished Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed... ...opportunities.Managing other Directors and/or Senior Directors responsible for Atherosclerosis...Full timeFor contractorsLocal areaFlexible hours$76k - $125.3k
...that need to be addressed or escalated to ensure tax returns, tax research, tax accounting and tax projects are timely and accurately... ...appropriately escalating complex tax and client relationship matters to senior management and subject-matter professionals, coordinating...SeniorFull timeSummer holidayFlexible hours$140k - $165k
...What You Will Do: GFT is seeking a Principal Environmental Scientist to join our growing Environmental Practice. This role follows a hybrid work model, requiring regular attendance at our Morristown, NJ and New York offices. GFT's Environmental team delivers integrated...PrincipalFull timeLocal areaRemote work- ...The Senior Principal Analyst in Market & Regulatory Services (“MRS”) Strategic Innovation & Research performs essential analysis and research to enable MRS to effectively innovate and expand its portfolio through securities industry experience, market research, operational...PrincipalSeniorFull timeTemporary workPart timeWork at officeLocal areaImmediate start
- Aquestive Therapeutics is looking for a hands-on scientific professional to evaluate, design, and execute formulation development plans. The role involves creating strategies for drug absorption and delivery across various routes, including oral and topical. This position...Senior
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Principal Scientist, Clinical Research, Immunology. Be the first to apply!
- scientist Rahway, NJ
- cell culture scientist Rahway, NJ
- lab scientist Rahway, NJ
- research scientist - biology Rahway, NJ
- r&d scientist Rahway, NJ
- applied scientist Rahway, NJ
- molecular biology scientist Rahway, NJ
- regulatory scientist Rahway, NJ
- senior research scientist Rahway, NJ
- senior scientist Rahway, NJ


