1 - 12 of 12 Jobs

Senior Statistical Programmer

Jobot

San Francisco, California, USA

Full-time

This Jobot Job is hosted by: Andrew Castillo Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $110,000 - $150,000 per year A bit about us: Our Client is a full-service contract research organization optimally sized to deliver results from clinical research with agility and adaptability. Why join us? Benefits: Hybrid work 401(k) 401(k) matching Health insurance Paid time off Professional development assistance Retirement plan Schedule: Monda

Principal Statistical Programmer - Late Phase

Zachary Piper Solutions, LLC

Raleigh, North Carolina, USA

Full-time

Piper Companies is looking for an experienced Principal/Senior Statistical Programmer to join a well-established, global clinical research organization focused on improving the drug development process and access to therapeutics. Responsibilities of the Principal/Senior Statistical Programmer: Support Phase II & teams with tasks related to submissions work End-to-End ADaM/TFL efficacy programming Creating submissions packages, eCDT packages, P21 reports, define.xml, SDRG/ADRG, etc. Qualificat

Principal Statistical Programmer

Zachary Piper Solutions, LLC

Remote

Full-time

Piper Companies is currently looking for a Principal Statistical Programmer to work remotely within the US. The Principal Statistical Programmer will provide technical expertise to create programming solutions across the statistical team for complex projects. Responsibilities for the Principal Statistical Programmer include: Design and develop custom programming code in order to produce summary tables, graphs, and datasets Develop programming specifications for complex studies Fulfil project

Senior Statistical Programmer - PKPD Early Phase

Zachary Piper Solutions, LLC

Raleigh, North Carolina, USA

Full-time

Piper Companies is looking for an experienced Senior Statistical Programmer (PK/PD) to join a well-established, global clinical research organization focused on improving the drug development process and access to therapeutics. Responsibilities of the Senior Statistical Programmer: Provide statistical programming expertise in PKPD such as generating ADPC, ADPP and POPPK datasets & NCA TFLs Pooling of PK Parameters and relevant safety ADaM datasets Assist in establishing standardized programming

Senior Manager, Biostatistics

AstraZeneca

Boston, Massachusetts, USA

Full-time

This is what you will do: The Senior Manager Biostatistics is responsible for statistical activities in support of clinical trials, including but not limited to the following: contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data. You will be responsible for: Collaborates with Clinical Development, Clinical Pharmacology, Regulatory and Clinical Operations expertise are

Associate Director, Biostatistics

AstraZeneca

Boston, Massachusetts, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Associate Director, Biostatistics

AstraZeneca

Boston, Massachusetts, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Associate Director, Biostatistics

AstraZeneca

Boston, Massachusetts, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Associate Director, Biostatistics

AstraZeneca

Boston, Massachusetts, USA

Full-time

This is what you will do: The Associate Director, Biostatistics oversees all biostatistics activities for one or more clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and reports and regulatory submissions. Independently provides strategic statistical input to drug development including feasibility assessments, development plans, complex study designs, cross-study statistical methodology, interpretations, regulatory submissions and follow up. Contributes

Clinical Database Developer

General Dynamics Information Technology

Frederick, Maryland, USA

Full-time

GDIT's Military Health team is hiring Clinical Database Developer to support the Office of Regulated Activities (ORA) under the DoD (Dept. of Army) located at Ft. Detrick in Frederick, Maryland. The Office of Regulated Activities (ORA) is a multidisciplinary team of regulatory affairs, compliance, and clinical support professionals dedicated to supporting the USAMRDC mission of developing Food and Drug Administration regulated medical products for the Warfighter. The ORA provides full-service,

Data Architect - NextGen QMS

Eli Lilly and Company

Indianapolis, Indiana, USA

Full-time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

SAS Programmer (NO C2C)

Juno Search Partners

Philadelphia, Pennsylvania, USA

Contract

Juno Search Partners is a certified women-founded and women-led talent solutions firm with extensive experience in the placement of accounting, administrative, finance, human resources, legal, marketing, operations, and technology candidates nationwide. We are looking for a passionate and experienced SAS Programmer! SAS Programmers are responsible for transforming raw data into analyzing datasets, providing Tables, Listings, and Figures (TLFs), and maintaining and improving analysis algorithms a