32 Results for

Biostatistics Jobs in North Branch, NJ

Jobs

Basking Ridge, NJ17 days ago

Mentoring and Coaching Junior Statisticians: Mentoring the study level statisticians for the assigned projects to ensure optimal statistical handling and quality deliverables including Protocol Development, Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and Clinical Study Report (CSR). Drug Development Strategy: Provides input to the clinical development plan to ensure the overall strategy can deliver the pre-specified product profile, is logical, scientifically sound, proposed studies have appropriate designs, efficacy and safety information to be collected meet regulatory agencies’ requirements for countries and regions the drug is to be submitted.

Basking Ridge, NJ17 days ago

$201,840–$302,760 Per Year
Full-time

Basking Ridge, NJ17 days ago

$168,000–$252,000 Per Year
Full-time

Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical analysis accuracy validation, results interpretation and CSR input and review. May participate in meeting or teleconferences with Health Authorities Global BDO Strategy to Improve Drug Development: Primarily participates and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company.

Basking Ridge, NJ15 days ago

$271,500–$452,500 Per Year
Full-time

Provides regular status updates on projects, metrics and KPIs to Head of BDM and BDM LT External Vendor Oversight: Provides oversight of and is accountable for the quality/performance and budget, resources and timelines across the department and ensures timely delivery of high-quality deliverables at reasonable cost. This role also serves as a key member of the BDM leadership team, contributing to BDM broader organizational strategy, cross-functional decision-making, and the advancement of BDM objectives beyond the Biostatistics function.

Basking Ridge, NJ17 days ago

$275,250–$458,750 Per Year
Full-time

The individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk throughout the lifecycle of the drug. Depending on the status of development of the compound, lead and medical-scientifically direct a team of physicians and scientists responsible for a compound/product including project-specific training and coaching of team members and review of team output cross-functionally.

Lawrenceville, NJ30+ days ago

Responsibilities:Data Analytics and ReportingBuild and continuously improve data analytics through supporting models that provide insights into efficiency, quality, stakeholder feedback, and key performance indicators to drive timely and informed decision making. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence applies a combination of life sciences strategy, leadership, and reporting/visualization experience to drive successful servicing of information needs across PS.

New!

Parsippany-Troy Hills, NJ1 day ago

$120,000–$160,000 Per Year
Full-time

The position requires strong technical expertise in statistics and SAS programming, with the ability to independently develop Statistical Analysis Plans (SAPs), execute and validate statistical analyses, and prepare statistical components of clinical study reports (CSRs). The right candidate can translate statistical outputs into clinically meaningful interpretations and communicate findings clearly to both technical and non-technical audiences.

Basking Ridge, NJ23 days ago

$201.84–$302.76

Mentoring and Coaching Junior Statisticians: Mentoring the study level statisticians for the assigned projects to ensure optimal statistical handling and quality deliverables including Protocol Development, Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and Clinical Study Report (CSR). Drug Development Strategy: Provides input to the clinical development plan to ensure the overall strategy can deliver the pre-specified product profile, is logical, scientifically sound, proposed studies have appropriate designs, efficacy and safety information to be collected meet regulatory agencies requirements for countries and regions the drug is to be submitted.

New Brunswick, NJ30+ days ago

CORE VALUES Curiosity and Discovery encouraging an environment of continuous inquiry, creativity, and innovation to generate new knowledge Integrity earning the trust of those we serve and each other through honesty, transparency, accountability, and continuous reflection Collaboration approaching all opportunities with an understanding that together we are better and can achieve more, promoting and maintaining an environment of teamwork and shared knowledge Respect and Caring consistently demonstrating caring compassion and respect through our words and actions Perseverance maintaining an unwavering commitment to our mission, embracing change, overcoming obstacles, and creating and recreating the path to achieve our goals. MISSION Our mission is to accelerate scientific discovery focused on understanding cancer, innovating cancer treatment, and improving cancer prevention to provide outstanding novel and compassionate patient care to provide evidence-based and culturally informed education to physicians, nurses, researchers, staff, and the community, and to achieve cancer health equity in our state through outreach to and engagement of our extraordinarily diverse communities.

Raritan, NJ30+ days ago

Remote

Full-time

The Senior Scientist, Biostatistics will support the Oncology Therapeutic Area with a focus on: solid tumors or hematologic malignancies; cancer interception with the goal of developing products that interrupt the carcinogenic process; biomarkers that may help guide targeted, individualized use of our therapies; as well as safe and effective identification and treatment of early changes in the tumor microenvironment. Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America.

Warren, NJ30+ days ago

D. in statistics or related discipline with 10+ years of experience (or MS in statistics or related discipline with 15+ years) in the biotechnology, pharmaceutical or health related industry, including significant interaction with both FDA and EMEA, history of successful project and people management (6+ years), and expertise in multiple therapeutic areas. They must also possess excellent communication skills to interface with senior leadership on behalf of the department and work closely with medical study directors to provide and receive direction on clinical programs and have the ability to influence the medical and clinical teams.

Princeton, NJ30+ days ago

Contribute to the development and implementation of innovation in statistical methodology and trial design; perform simulations to assess various study design options and analysis approaches. Currently they are seeking an Associate Director of Biostatistics to support registration-directed clinical development programs and global regulatory submissions.

Piscataway, NJ30+ days ago

$60–$80 Per Hour

Immunization Requirements Under Policy 100.3.1 Immunization Policy for Covered Individuals if employment will commence during Flu Season Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season unless the University has granted the individual a medical or religious exemption. The specific benefits vary based on the position and may include: • Medical • Prescription drug • Dental coverage • Paid vacation • Holidays • Various leave programs • Competitive retirement benefits including defined contribution plans and voluntary tax-deferred savings options • Employee and dependent educational benefits when applicable • Life insurance coverage • Employee discount programs.

Bridgewater, NJ30+ days ago

Remote

To assist in identifying candidates with qualifications matching those required and/or preferred for this role, Insmed uses an Automated Employment Decision Tool ("AEDT") that employs artificial intelligence to analyze and score information provided in resumes and application materials including, but not limited to, skills, work experience, education, and job-related qualifications. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, youll be part of a community that prioritizes the human experience, celebrates curiosity, and values every persons contributions to meaningful progress.

Princeton, NJ30+ days ago

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Newark, NJ30+ days ago

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 protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc.

Bridgewater, NJ30+ days ago

Generate, validate, and/or review tables, figures and listings to support the statistical analysis of clinical trials data in support of regulatory submissions and publications. Extensive knowledge of SAS Macros highly preferred, in addition to knowledge of Base SAS, SAS/STAT, SAS/Graph, SAS/SQL and SAS/ODS.

Bridgewater, NJ30+ days ago

Somerset, New Jersey23 days ago

$72,000–$72,000

Led by former FDA experts and industry experts, R&G US can provide end-to-end services in strategic planning, clinical trial design, statistical analysis, SAS programming, data management, medical writing, medical monitoring, pharmacovigilance, and Data Monitoring Committee services. R&G US's goal is to provide the best service to the clients and work as one team to lower costs, shorten development time, and increase the success probability of products.

Edison, NJ30+ days ago

Princeton, NJ17 days ago

Full-time

You will work closely with cross-functional teams, including clinical, regulatory, and international colleagues, to contribute to statistical analyses that inform decision-making across the clinical pipeline. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).

New!

Florham Park, New Jersey2 days ago

$151–$198 Per Year

Competencies & capabilities: Proven expertise in epidemiologic methods, database strategy, and observational research designs; Strong record of regulatory engagement, payer influence, and external thought leadership; Prior line management experience with ability to mentor and develop scientific staff; Executive presence with excellent communication skills across technical and non-technical audiences. Purpose of travel (e.g., conferences, client meetings, site visits): Travel as needed for global and regional leadership meetings, cross-functional planning sessions, regulatory or payer meetings, scientific conferences, and key stakeholder engagements.

Newark, NJ9 days ago

Provides general infrastructure support to the Department (presents / teaches at the department meetings, contributes to other general department documents or policies, assists with newsletter, helps in department libraries, or trains new hires). Supports the department by directly contributing to simple or moderately complex study protocols and bid defenses, including organizing teams and implementing strategies to ensure process and programming efficiencies.

Newark, NJ9 days ago

Princeton, NJ30+ days ago

Full-time

For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. The Role : The Senior Director acts as a high-level statistical expert supporting the clinical development of compounds as therapeutic area lead, compound lead and/or indication lead for both early and late-stage programs and may also act as trial responsible statistician with responsibilities as described below.

New!

Basking Ridge, NJ1 day ago

Requires strong oral and written communication, expertise in analyzing clinical processes and data, experience meeting with and influencing senior-level leaders at all levels, adept at preparing and presenting high-quality presentations and leading workshops, and being a proactive, self-driven team player. Provide support for biostatisticians, translational scientists, researchers, and other clinical data analysts in the governance process for accessing clinical data (no biostatistics or translational science experience needed).

Spring House, PA30+ days ago

Remote

Full-time

The Portfolio Lead in Clinical & Statistical Programming ( C&SP) also provides leadership and expertise in relevant technical areas and subject matter in support of process improvement, maintenance, and innovation initiatives and develops strong and productive working relationships with key stakeholders within IDAR in addition to broader partners, external suppliers, and industry groups. This position is responsible for formulating the programming strategy across a portfolio of one or more programs, compounds, indications, disease areas within a delivery unit, with accountability for operational oversight and effective planning and execution of programming activities for their assigned portfolio while ensuring effective partnership with and management of stakeholders.

Trenton, NJ30+ days ago

The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regulatory reporting efforts in line with the overall WWPS needs. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence applies a combination of life sciences strategy, leadership, and reporting/visualization experience to drive successful servicing of information needs across WWPS.

Parsippany, New Jersey30+ days ago

$141,000–$194,000 Per Year

The Associate Director is versed in statistical programming languages such as SAS, R, Python, etc. to perform programming in processing data at various levels, verifies analytical datasets, and applies conventional and novel statistical methods to summarize data and generate clinically meaningful results. Working closely with his/her manager, the Associate Director designs pain management studies of clinical/economic burden of diseases, unmet needs of patients, comparative effectiveness of treatments on economic/health outcomes across treatments.

Raritan, NJ30+ days ago

Remote

Full-time

Cambridge, Massachusetts, United States of America, Horsham, Pennsylvania, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America. OHDA's mission is to improve the lives of individuals and quality of healthcare by efficiently generating real-world evidence from the world's observational health data, transparently disseminating evidence-based insights to real-world decision-makers, and objectively advancing the science and technology behind reliable, reproducible real-world analytics.

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Biostatistics Jobs in North Branch, NJ

Director, Early Phase Biostatistics (m/f/d) Daiichi Sankyo, Inc.

Director, Early Phase Biostatistics Daiichi Sankyo, Inc.

Associate Director, Biostatistics (Late Stage) Daiichi Sankyo, Inc.

Head of Global Biostatistics Daiichi Sankyo, Inc.

Senior Director, Clinical Safety MD Daiichi Sankyo, Inc.

Pharmacovigilance (PV) Analytics and Reporting Specialist ECLARO

Senior Biostatistician Canfield Scientific, Inc.

Director, Early Phase Biostatistics Daiichi Sankyo Co Ltd

Research Teaching Specialist IV (Biostatistics and Epidemiology) Rutgers The State University of New Jersey

Senior Scientist, Biostatistics - Oncology Johnson and Johnson

Senior Director, Biostatistics - Immunology & Inflammation Regeneron Pharmaceuticals Inc

Associate Director Biostatistics Penfield Search Partners

Adjunct Instructor (Per Diem) Biostatistics Rutgers The State University of New Jersey

Director, Biostatistics Insmed Inc

Director, Biostatistics Bristol-Myers Squibb Co

Senior Principal Statistical Programmer Katalyst Healthcares & Life Sciences

Sr. Statistical Programmer Katalyst Healthcares & Life Sciences

Sr. Statistical Programmer Karwell Technologies

Statistical Analyst and SAS Programmer R&G US Inc.

Senior Statistician Karwell Technologies

Senior Statistician Katalyst Healthcares & Life Sciences

Biostatistician Systimmune

Senior Director, Epidemiology & Real World Evidence Contractor Shionogi Inc.

Statistician Karwell Technologies

Statistician Katalyst Healthcares & Life Sciences

Senior Director, Statistician Genmab

Clinical Data Governance Lead Aequor Technologies LLC

Principal Portfolio Lead, Statistical Programming - Oncology Johnson and Johnson

C08 - MEDICAL AND REGULATORY AFFAIRS / PHARMACOVIG - PHARMACOVIGILANCE SPECIALIST TechDigital Corporation

Associate Director, RWE Analytics Pacira Pharmaceuticals, Inc.

Manager, Observational Health Data Analytics Johnson and Johnson

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