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King of Prussia, Pennsylvania

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Today

DUTIES: Proficient to write SAS codes to produce CDISC complaint datasets. Create statistical analysis outputs to be used in support of final reports, abstracts, posters, manuscripts, adhocs and other clinical publications. Write QC SAS programs for Dataset, Tables, Listings, and Figures following the departmental QC procedures and good programming practices. Write programs for ISS, ISE and pooled datasets. Revise programs for corrections, enhancements, or system environment changes. Proficient

Full-time

USD 96,013.00 per year

Clinical SAS SDTM

North Wales, Pennsylvania

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Today

HCL Technologies Limited Key Responsibilities: * Create advanced SAS macros, templates, and utilities for efficient data processing * Act as the primary programming point of contact for biostatisticians and study teams * Perform peer review of code and documentation for accuracy and traceability * Review CRF (Case Report Form) annotations and data specifications. * Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines. Skill Requirements: * Extensive programming experi

Full-time, Contract

To define

Senior Programmer, Clinical Data Evaluation

King of Prussia, Pennsylvania

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Today

Position Purpose: The Senior Programmer for Data Validation supports cross-functional teams such as Statistics, Data Management and Standards by overseeing and ensuring the quality of clinical data build and programming activities across in-house, hybrid, and vendor-supported studies. The role focuses on governance, review, and validation of deliverables to ensure alignment with CSL standards, regulatory requirements, and industry best practices. The incumbent applies strong expertise in CDASH a

Full-time

Compensation information provided in the description

Associate Director, Biostatistics

King of Prussia, Pennsylvania

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Today

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions, and is accountable for the statistical deliverables within the program. 1 Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data

Full-time

Principal Stat Programmer

King of Prussia, Pennsylvania

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Today

The Principal Statistical Programmer is responsible for providing leadership and hands-on support in the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. The individual will work closely with the Associate Director, Director, and Statistical Programmers to build internal programming tools. This individual, working closely with the study team, will be responsible for review and acceptance of contract research organizatio

Full-time

Sr. Clinical Data Analyst (Remote)

Remote

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10d ago

DivIHN (pronounced divine) is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have been trusting us to help build their teams with exceptional temporary and permanent talent. Visit us at to learn more and view our open positions. Please apply o

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Contract, Third Party

Depends on Experience

Statistical Programmer (Remote)

Remote

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Today

A biotech company in North Carolina is seeking a new Statistical Programmer to join their team remotely, developing SAS programming deliverables for clinical study analysis and reporting. This is a Remote opportunity. Responsibilities: Programming and validating tables, listings, figures, and derived datasets using SAS Developing SDTM and ADaM datasets and supporting documentation Preparing and reviewing mapping specifications and annotated case report forms (CRFs) Performing quality control an

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Contract

Associate Director, Programming (Macros & Automation CDISC)

King of Prussia, Pennsylvania

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Today

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we?re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, Programming (Macros & Automation)? The job is in our Waltham MA, King of Prussia PA or Glattbrugg Sw

Full-time

Compensation information provided in the description

Principal Programmer ( Data Oversight & Standards)

King of Prussia, Pennsylvania

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Today

Principal Programmer - Clinical Data Oversight & Standards provides leadership and oversight for clinical data build, programming, and vendor deliverables across in-house, hybrid, and outsourced studies, ensuring alignment with CSL standards, regulatory requirements, and industry best practices. The role drives governance, review, and validation processes; leads the implementation of CDASH and SDTM standards; and oversees scalable validation frameworks and data quality controls. Additionally, i

Full-time

Compensation information provided in the description

Principal Programmer ( Data Oversight & Standards)

King of Prussia, Pennsylvania

•

Today

Full-time

Compensation information provided in the description

Clinical Data Management Technical Specialist

Remote or Hybrid

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Today

A pharma company in Massachusetts is looking to fill an immediate remote/contract need with the addition of a new Clinical Data Management Technical Specialist to their team. In this role, the Clinical Data Management Technical Specialist will be responsible for providing technical expertise and project management support for the Clinical Data Management team. No agency candidates please. Responsibilities: Performing and reviewing clinical data mappings from multiple data sources Liaising with e

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Third Party, Contract

$64 - $64 per hour

Cardiac Rhythm Management Technical Field Engineer - Seattle, WA

Remote or Seattle, Washington

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Today

We anticipate the application window for this opening will close on - 30 May 2026 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life We are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired wil

Full-time

USD 84,000.00 - 126,000.00 per year

Cardiac Rhythm Management Technical Field Engineer - Houston, TX

Remote or Houston, Texas

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Today

We anticipate the application window for this opening will close on - 27 May 2026 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life We are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired wil

Full-time

USD 84,000.00 - 126,000.00 per year

Cardiac Rhythm Management Technical Field Engineer - Southern/Western MA, Rhode Island

Remote or Worcester, Massachusetts

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Today

We anticipate the application window for this opening will close on - 29 May 2026 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life We are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired wil

Full-time

USD 90,000.00 - 114,000.00 per year

Real World Evidence (RWE) Analyst - Remote

Remote or Santa Monica, California

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Today

ApTask Global Workforce (AGW) is seeking a Senior Manager - Medical Affairs with a Biopharmaceutical company. This is a 6+ month contract opportunity with our client located in Santa Monica, CA. This is Remote position. Summary: The RWE Senior Manager will contribute to the Real-World Evidence/Health Economic Outcomes Research (RWE/HEOR) Team to support the broader Evidence Generation Team. This role involves conducting timely and rigorous analysis of real-world data (RWD) to address critical re

Full-time

USD 86.33 per hour

Clinical Biostatistician II

Remote

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Today

Help us change lives At Exact Sciences, we're helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you're working to help others. The Clinical Biostatistician II with general guidance from more experienced Statisticians, works individually and in collab

Full-time

USD 102,400.00 - 153,600.00 per year

Senior Provider Network Intelligence Analyst

Remote or Arizona

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Today

Department Name: Provider Network Intellig&Oper Work Shift: Day Job Category: Marketing and Communications Estimated Pay Range: $43.77 - $72.95 / hourBanner Health is committed to pay equity and transparency. The posted compensation range is a reasonable estimate that extends from the lowest to the highest pay Banner Health in good faith believes it might pay for this particular job, based on the circumstances at the time of posting.This range is based on possible base salaries and does not

Full-time

USD 43.77 - 72.95 per hour

Associate Director, Biostatistics (4)

King of Prussia, Pennsylvania

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Today

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions, and is accountable for the statistical deliverables within the program. Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area.Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data ana

Full-time

Associate Director, Biostatistics (2)

King of Prussia, Pennsylvania

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Today

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the program. ( Positions available supporting multiple Therapeutic Areas available ) Main Responsibilities: Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical

Full-time

Epidemiologist/Real World Evidence (RWE) Analyst

Remote

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5d ago

About Nexinfo NexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors. They offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions. The company aims to help businesses across industries achieve their goals through industry best practices, lean process design, and advanced software solutions. Their ERP-related services address challenges s

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Third Party, Contract

$80 - $90

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