Scientist, Clinical Schedule Manager, Statistical Programming (Hybrid)
$96.2k - $151.4kFull-time
Merck & Co.
Job Description In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Clinical Schedule Management is in the Biostatistics and Research Decision Sciences (BARDS) department at our Research & Development division, which supports the targeting, discovery, development, manufacturing, and marketing of drugs and vaccines for the benefit of patients and global public health. Clinical Schedule Managers have a key role in our clinical trials and support all therapeutic areas and every phase of drug development across Research & Development. - This position contributes to the overall management of clinical schedules in support of clinical study randomization and data unblinding under the guidance of a more experienced staff member. The clinical schedule manager will collaborate with biostatisticians within BARDS, as well as members of data management, clinical supplies, and clinical operations to develop requirements for randomization and trial supply management systems. -
Clinical Trials, Communication, Detail-Oriented, Stakeholder Relationship Management, Statistics, Teamwork Preferred Skills:
AI Agents, Artificial Intelligence (AI), Confidential Data Handling 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. 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 Rights EEOC GINA Supplement• We 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 Acts The salary range for this role is
$96,200.00 - $151,400.00 This 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 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:
No relocation VISA Sponsorship:
No Travel Requirements:
10% Flexible Work Arrangements:
Hybrid Shift:
Not Indicated Valid Driving License:
No Hazardous Material(s):
n/a Job Posting End Date:
09/4/2026
*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: R414221
Primary Activities:
- Contribute to clinical schedule design, generation, review, and distribution
- Ensure compliance for maintaining blinding during study conduct
- Perform activities related to the support of unblinding for data analysis
- Assure high quality and timely deliverables
- Communicate and collaborate effectively with operational staff and partners globally
Education and Minimum Requirement:
- BA/BS in Computer or Data Science, Statistics, Life Sciences, or related field with a minimum of 2 years of pharmaceutical drug development experience
- MS in Computer or Data Science, Statistics, Life Sciences, or related field
Skills and Experience:
- Working knowledge of the clinical development process and clinical study design
- Basic understanding of statistics, clinical, medical monitoring, and data management concepts
- Good understanding of clinical trial randomization, blinding, and unblinding processes and tools
- Ability to organize, prioritize, and work efficiently and effectively in a constantly changing environment
- Ability to collaborate effectively with others on a team, take direction effectively, function independently, and complete tasks on time
- Written, oral, and presentation skills
- Motivated to advance career by investing in development activities and taking on responsibilities with increasing levels of challenge
- Knowledge of standard operating procedures and software development life cycle
- Knowledge in development of Analysis and Reporting deliverables for Research & Development projects
- Experience reviewing, writing, editing, and maintaining documentation
- Prior experience in developing AI agents and workflows is preferred
Clinical Trials, Communication, Detail-Oriented, Stakeholder Relationship Management, Statistics, Teamwork Preferred Skills:
AI Agents, Artificial Intelligence (AI), Confidential Data Handling 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. 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 Rights EEOC GINA Supplement• We 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 Acts The salary range for this role is
$96,200.00 - $151,400.00 This 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 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:
No relocation VISA Sponsorship:
No Travel Requirements:
10% Flexible Work Arrangements:
Hybrid Shift:
Not Indicated Valid Driving License:
No Hazardous Material(s):
n/a Job Posting End Date:
09/4/2026
*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: R414221
Vacancy posted 8 days ago
Similar jobs that could be interesting for youBased on the Scientist, Clinical Schedule Manager, Statistical Programming (Hybrid) in Rahway, NJ vacancy
$96.2k - $151.4k
...Development division, quantitative scientists, in partnership with other subject matter... ...of patients and global human health.Clinical Schedule Management is in the Biostatistics and Research... ...:BA/BS in Computer or Data Science, Statistics, Life Sciences, or related field...SuggestedFull timeFor contractorsLocal areaFlexible hours- Merck & Co. is seeking a Clinical Schedule Manager in BARDS within the R&D division. The role supports clinical schedule design across therapeutic... ..., timely deliverables, and ongoing professional development within a hybrid work environment. #J-18808-Ljbffr Merck & Co.Suggested
$142.4k - $224.1k
...Associate Principal Scientist to join our... ...Development Sciences and Clinical Supply (DSCS)... ..., data management, version control,... ...laden systems.Strong programming and data science... ...frameworks, including statistical design and analysis... ...networks (PINNs)Hybrid mechanistic / machine...SuggestedFull timeFor contractorsLocal areaFlexible hours$117k - $184.2k
...division.-Quantitative scientists, in partnership with... ...human health. The Clinical Safety Statistics (CSS) group within... ...communication, and effective management of product risk... ...support for program-level evaluation of... ...Flexible Work Arrangements Hybrid Shift Not Indicated...SuggestedFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$117k - $184.2k
Job DescriptionSenior Scientist, Statistical Programming - Rahway, NJ:Provide support to statistical programming... ...for late-stage drug/vaccine clinical development projects.Be accountable... ...requirements.Familiarity with clinical data management concepts.Effective interpersonal...SuggestedFull timeFor contractorsLocal areaVisa sponsorshipFlexible hours$117k - $184.2k
...Development division. Quantitative scientists, in partnership with other... ...global human health.The Clinical Safety Statistics (CSS) group within BARDS... ..., and effective management of product risk profiles in... ...Provide statistical support for program-level evaluation of...Full timeFor contractorsLocal areaFlexible hours$150.5k - $245.5k
...diseases. We are seeking a Senior Manager, Statistical Programming to join our Statistical Programming... ...Cambridge, MA Work model/flexibility: hybrid-onsite Discover your role:... ...bring advanced SAS skills honed in a clinical data environment, ideally across...WorldwideRegeneron Pharmaceuticals
Warren, NJ1 day ago$144.37k - $224.1k
Job DescriptionAssociate Principal Scientist, Statistical Programming - Rahway, NJ:Provide high quality statistical... ...synthesize preclinical / clinical data into analysis ready structures... ...required.Must possess strong project management skills; excellent interpersonal...Full timeFor contractorsLocal area$117k - $184.2k
...Development division, quantitative scientists, in partnership with other... ...: This position supports statistical programming activities for late-stage drug/vaccine clinical development projects. This may... ...programming practices Maintain and manage a project plan including...Full timeFor contractorsLocal areaRemote workWorldwideRelocationVisa sponsorshipFlexible hoursShift workMerck & Co.
Rahway, NJ14 days ago$96.2k - $151.4k
...planning and execution of one or more clinical trials and assists the Lead Clinical Scientist and study team with the... ...ICF documents/amendments, data management deliverables) . - May interact... ...0% Flexible Work Arrangements: Hybrid Shift: Not Indicated Valid Driving...For contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$90.2k - $128.5k
Location: Clark, NJ (Hybrid) Hello, we’re L’Or... ...-driven Senior Scientist II - Cognitive Science... ...and the advanced statistical integration of... ...requires strong project management,proficiencyin scientific programming (Python/R),... ...multiple testing schedules and deliver reliable...Work experience placementSummer workWork from homeFlexible hours2 days per week$117k - $184.2k
...Description Provide support to statistical programming activities for late-stage drug/vaccine clinical development projects. Be... ...one or more projects. Senior Scientist, Statistical Programming - Rahway... ...with clinical data management concepts. Effective interpersonal...For contractorsLocal areaFlexible hours$255.8k - $402.7k
Job DescriptionJob DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for planning... ...). The Clinical Director may manage the entire cycle of clinical development... ..., regulatory affairs, statistics, and manufacturing to manage clinical...Full timeFor contractorsLocal areaFlexible hours$144.37k - $224.1k
...Description Associate Principal Scientist, Statistical Programming - Rahway, NJ: - Lead statistical programming... ...multiple and/or complex late-stage clinical trial development programs.... ...biostatisticians, project leads, data managers, and other stakeholders in ensuring...Full timeFor contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift workMerck & Co.
Rahway, NJ14 days ago$145.48k - $224.1k
...Job Description Responsibilities: Provide high quality statistical programming analysis and reporting deliverables for global stakeholders... ...with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data...Full timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift workMerck & Co.
Rahway, NJ14 days ago$87.3k - $137.4k
...DescriptionOur Research Scientists are our Inventors.... ...colleagues in Discovery, Pre-clinical, Early Development,... ...understanding of statistical methods and data... ...intelligence; proficiency with programming languages#BPRD #PRD... ...Scale Up, Process Scheduling, Product Development,...Full timeFor contractorsLocal areaFlexible hours$128.6k - $210k
...life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single...Permanent employmentFor contractorsWork experience placementWorldwideShift workRegeneron Pharmaceuticals
Warren, NJ5 days ago$310.9k
...Director (Distinguished Scientist) has primary... ...and directing of clinical research activities... ...Executive Director will manage and oversee the... ...development of program strategy and design... ...affairs, statistics, and manufacturing... ...Arrangements: Hybrid Shift: Not Indicated...Full timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- Everforth Apex Systems seeks an AI Project Manager to lead governance, planning, and execution for AI-enabled Communications Surveillance... ...and executive-facing collaboration across multiple priorities. Hybrid work with on-site days is expected. #J-18808-Ljbffr Apex...
$190.8k - $300.3k
...division, quantitative scientists, in partnership... ...knowledge of statistical methodology, experimental... ...and data management; a general understanding... ...; and with good clinical trial experience... ..., Statistical Programming, our Research &... ...Arrangements: Hybrid Shift: Not...Full timeFor contractorsWork experience placementLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift workMerck & Co.
Rahway, NJ14 days ago- ...Edison, New Jersey (Hybrid) Position Overview... ...integrated behavioral health program serving older adults... ...opportunity for a clinically strong and operationally... ...healthcare environments. Schedule Full-time Hybrid... ...team management. Demonstrated success...Full time
The Provider Finder
Edison, NJ7 days ago $117k - $184.2k
...Job Description Senior Scientist, Human Factors The Human... ..., and lifecycle management. This person will lead and... ...Partner with marketing, program management, clinical, safety, regulatory, manufacturing... ...Flexible Work Arrangements: Hybrid Shift: Not Indicated...Full timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$190.8k - $300.3k
...DescriptionThe Senior Director, Clinical Science - Hematology is responsible... ...spanning multiple studies, programs, and assets. Reporting to the Executive... ...have responsibility for direct management and development of multiple Clinical Scientists and is expected to provide...Full timeFor contractorsLocal areaFlexible hours$129k - $203.1k
Job DescriptionJob Description:The Global Clinical Supply (GCS) organization manages the “end-to-end” clinical supply for the company’s portfolio. GCS... ...customer satisfaction, and efficiency.Monitor the production schedule on a weekly, monthly, and quarterly basis while...Full timeFor contractorsLocal areaWorldwideFlexible hours$173.2k - $272.6k
...closely with colleagues in Discovery, Pre-clinical, Early Development, Analytical,... ...to influence the field.As a Principal Scientist you will have the opportunity to influence... ...Biophysical, mechanistic and facility modeling; statistical analysis, data-science, machine...Full timeFor contractorsLocal areaFlexible hours$169.54k
...Development, LLCJob Title: Principal Scientist, Data ScienceJob Code: A011.4... ...arm studies, synthetic and hybrid control arm studies,... ...Epidemiology, Biostatistics, Statistics or related quantitative field... ...Company’s long-term incentive program.Subject to the terms of their...Full timeLocal areaImmediate startRemote work$117k - $184.2k
...a highly skilled and motivated Senior Scientist to join our R&D team.Purpose of the RoleThe... ....Other responsibilities include statistical experimental design & data analysis, authoring... ...other functional areas (e.g. project management, manufacturing, quality, regulatory...Full timeFor contractorsLocal areaFlexible hours$117k - $184.2k
Job DescriptionSenior Scientist, Biostatistics - Rahway, NJ: Serve as statistical representative in the... ...functional teams for the clinical trial planning,... ...with the statistical programming staff to ensure that all... ...to the project team, management, regulatory agencies,...Full timeFor contractorsLocal area$173.2k - $272.6k
...colleagues in Discovery, Pre-clinical and Early Development... ...as a Principal Scientist. In this role, the successful... ...and metabolism, DOE statistics and computational... ...leading cross functional, program development teams.... ...Engineering, Clinical Supplies Management, Clinical Trials,...Full timeFor contractorsLocal areaFlexible hours$173.2k - $272.6k
...colleagues in Discovery, Pre-clinical and Early Development to rapidly... ...join our team as a Principal Scientist. In this role, the successful... ...biology and metabolism, DOE statistics and computational fluid... ...Experience leading cross functional, program development teams.Required...Full timeFor contractorsLocal areaFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Scientist, Clinical Schedule Manager, Statistical Programming (Hybrid). Be the first to apply!
Related searches
- materials scientist Rahway, NJ
- health scientist Rahway, NJ
- quality control scientist Rahway, NJ
- deep learning scientist Rahway, NJ
- application scientist Rahway, NJ
- senior analytical scientist Rahway, NJ
- decision scientist Rahway, NJ
- principal scientist Rahway, NJ
- scientist 1 Rahway, NJ
- associate scientist Rahway, NJ