Senior Biostatistician - Regulatory & Adaptive Trial Design
$130k - $140kTata Consultancy Services Limited
Tata Consultancy Services Limited is seeking a statistical expert in Edison, New Jersey. The role involves designing clinical studies, preparing regulatory-grade reports, and defining statistical analysis plans. Must have strong knowledge of SAS and regulatory standards. The ideal candidate holds a Bachelor of Computer Science, has proven experience in statistical methodologies, and is capable of producing analysis datasets. A competitive salary range of $130,000 to $140,000 per year is offered. #J-18808-Ljbffr Tata Consultancy Services Limited
- Vitalief in New Brunswick, NJ is seeking a dedicated Senior Clinical Research Coordinator to support clinical trials, particularly in Oncology. The role involves patient interaction, data management, and ensuring regulatory compliance. Candidates must have a Bachelor’s...SeniorRegulatoryFull time
$130k - $140k
...statistical methodologies, SAS, Regulatory Standards. Roles & Responsibilities Designing and powering clinical and observational... .... Simulations for complex or adaptive designs. Preparing regulatory... ...margins for clinical trials. Calculation of sample sizes and...RegulatoryInterim role- ...role: Wells Fargo is seeking a Senior Information Security Engineer... ...team and contribute to the design, deployment, and ongoing support... ...and a willingness to adapt to evolving technologies will... ...Financial Crimes, Operational, Regulatory Compliance), which includes effectively...SeniorRegulatoryFull timeWork experience placementRelocation package
$282.2k
Senior Clinical Director (Senior Principal Scientist) Plan and direct clinical... ...studies including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Responsibilities... ...drugs. Plan clinical trials (designing, collaborating on operational...SeniorRegulatoryFor contractorsWorldwide$135.47k - $164.16k
...us. Position Summary The Senior Clinical Trial Manager (SCTM) is accountable for end-... ...). Coordinate the MOH responses with regulatory and central teams, as applicable. May... ...centers. Employees in remote-by-design or lab-based roles may be eligible for...SeniorRegulatoryHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$142.4k - $224.1k
...Associate Principal Scientist in Rahway, New Jersey, to lead and implement medical device design controls. This role requires strong expertise in product development, regulatory compliance, and cross-functional teamwork. The ideal candidate will have a B.A./B.S in engineering...SeniorRegulatory$210.4k - $331.1k
Job Overview Senior Principal Scientist (Sr. Director equivalent) - Immunology Biomarker... ...and scientific leadership in the design, execution, analysis, and communication... ...groups (clinical, discovery, translational, regulatory, bio‑stats, data science) to integrate scientific...SeniorRegulatoryFor contractors$142.4k - $224.1k
...seeking an Associate Principal Scientist in Rahway, NJ, to lead design verification strategies for innovative drug-device combination... ...project leadership, ensuring testing aligns with manufacturing and regulatory standards. The role requires a B.S. in Mechanical Engineering...SeniorRegulatory- ...SDTM/ADaM specifications, and knowledge of regulatory guidelines. Responsibilities include overseeing deliverables for clinical trials, conducting validations, and collaborating... ...study teams. This role operates at a mid-senior level in the pharmaceutical manufacturing...SeniorRegulatoryContract work
$144k - $176k
...MacDonald is seeking a highly experienced Senior Project Architect in Woodbridge Township... ...will possess expert-level architectural design skills and project management experience... ..., and ensuring compliance with all regulatory requirements. A comprehensive benefits package...SeniorRegulatory$65.35k - $70k
...Sustainability and Resiliency Planning Group as a Senior Planner. This position offers the... ...advance the County's long-term climate adaptation and infrastructure planning goals. The... ...manage and coordinate planning studies, regulatory reviews, and resiliency-focused projects...SeniorRegulatoryWork at officeLocal area- ...Senior Director, Biostatistics Regeneron is seeking... ...plans, study design, and operational aspects... ...project decisions and regulatory meetings. Serve as departmental... ...area related to clinical trial. Demonstrated... ...interpreting, modifying, and adapting procedures, practices,...SeniorRegulatory
$90k - $150k
...Ensures timely disposition of all claims in accordance with regulatory and statutory requirements. Maintain and manage a diary system... ...claim audits Attend depositions, settlement conferences and trials when necessary Performs other duties or special projects as...SeniorRegulatoryFull timeTemporary work$134.4k - $219.2k
...Senior Manager Product Lead Global Development Information Technology (GD IT) is seeking... ...transform the way clinical studies are designed, planned, and assessed. As the Product... ...ensuring alignment with business goals, regulatory standards, and data-privacy requirements...SeniorRegulatoryTemporary work$105k - $150k
...by the Mid Atlantic Real Estate Journal Join Our Team: Senior Civil Engineer Design/Build Construction Firm REDCOM, LLC, an award-... ...site plans, including all associated report preparation. Regulatory Compliance: Ensure all designs meet state, municipal, and...SeniorRegulatoryFull timeTemporary workWork from home- Hackensack Meridian Health Inc. is seeking a Clinical Research Coordinator to oversee clinical operations of trials, ensuring compliance with regulatory standards. This role requires a BA/BS in science or healthcare and at least 2 years of experience in clinical research...RegulatoryWork at office
$110k - $115k
...Description Job Description The Senior Azure Cloud & Network... ...responsible for leading the design, implementation, and governance... ...scalability, resilience, and regulatory compliance. While the... ...and documentation skills. ~ Adaptability in a large enterprise environment...SeniorRegulatoryTemporary workWork experience placement- ...Senior Clinical Research Coordinator Vitalief is a trusted partner working at the intersection... ...CROs across the research and clinical trials landscape. By blending deep subject... ...of IRB applications and preparation of regulatory documents, study documents and forms....SeniorRegulatoryFull timeTemporary workWork at officeRemote work
$134.4k - $219.2k
...The Senior Manager, Pharmacy Support Services (PSS) serves as... ..., compliant, and streamlined trial execution. You will partner... ...readiness, compliance with regulatory requirements, and optimal preparation... ...cross‑functional teams Adaptability, critical thinking, and a...SeniorRegulatoryLocal area$151.04k - $198.2k
...we want to hear from you. The Senior Oncology Sales Specialist is responsible... ..., meeting with key stakeholders, adapting quickly to internal/external... ..., approved promotional clinical trials, patient access to medication, and regulatory/compliance guidelines preferred....SeniorRegulatoryWork at officeLocal area$31.25 - $40.87 per hour
...Senior Administrative Assistant GZA GeoEnvironmental, Inc. (GZA) is seeking a Senior... ...preparation and distribution of paperwork for regulatory agency compliance, permits and reporting... ...environment. We are an ENR Top 500 Design firm focused on environmental,...SeniorRegulatoryHourly payContract work- ...Our strategic partnership is designed to combine the strengths and... ...is seeking a Sr. Manager, Biostatistician/Programmer as part of the... ...programs by transforming clinical trial data into high-quality... ...with internal standards and regulatory expectations. Support process...SeniorRegulatoryPermanent employmentFull timeFor contractorsInterim roleLocal areaWorldwide
- ...ADaM datasets for CNS clinical trials, ensuring traceability from... ...final clinical study reports, regulatory submissions, and client... ...critical thinker, willing to adapt and thrive in a fast‑paced CRO... ...collaborative team setting. Seniority level: Not Applicable | Employment...SeniorRegulatoryContract workInterim roleRemote workShift work
- Johnson & Johnson MedTech is seeking a Senior Counsel, Regulatory Law, based in New Brunswick, NJ. The role involves providing legal counsel on regulatory and compliance issues related to innovative MedTech products. The ideal candidate will have a J.D. and at least 7...SeniorRegulatory
$190.8k - $300.3k
Job Description Our Regulatory Affairs team in General Medicine advances... .... Position Overview The Senior Principal Scientist, Regulatory... ...agencies. The role requires adaptability to change and an entrepreneurial... ...agency approval for clinical trials Participate in regulatory...SeniorRegulatoryFor contractorsWork at officeLocal areaRemote workWorldwideMonday to Friday3 days per week- ...Inc. in New Jersey seeks a Sr. Director, Identity & Access Management to define and execute their IAM strategy. This role ensures regulatory compliance and protects sensitive data across the organization. The ideal candidate has extensive experience in IT and...SeniorRegulatory
- ...applications in New Brunswick, NJ. The role involves gathering business requirements, developing test plans, and ensuring adherence to regulatory standards. The ideal candidate will have over 10 years of experience and a strong understanding of GxP, FDA regulations, and GDPR...SeniorRegulatory
$81.7k - $135k
...Indirect Tax – Sales and Use – Senior Will you shape the... ...will advise on indirect tax regulatory changes and support compliance... ...Experience in operating model design and analysis. Understanding... ...performers who are analytical, adaptable, and proactive individuals who...SeniorRegulatorySummer holidayImmediate startFlexible hours- ...Design and implement features of our TMR data model Oversee cloud data migration to TMR and production deployment Contribute to technical design discussions and architecture decisions Write high-quality, testable code for chemical registration workflows...Senior
$117k - $184.2k
...laboratories portfolio of clinical trials. The GCS Planning... ...Project Manager (Protocol CSPM) designs strategic and operational plans... ...with clinical development, regulatory, quality, and supply chain... ...processes. Flexibility and adaptability to thrive in a fast‑paced dynamic...SeniorRegulatory
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