CDISC jobs in Philadephia, PA

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 Principal Biostatistician? The job is in our King of Prussia, PA, Waltham MA and Maidenhead UK office. This is a hybrid

Full-time

Sr. SAS Programmer

Wilmington, Delaware

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Today

Job Description: The Sr. SAS Programmer provides PKPD programming aspects of pharmacokinetics, pharmacodynamics data management by timely completion and high quality of all required deliverables. Responsibilities: Prepare data for state-of-the-art analysis, such as PPK, PKPD, exposure-response (efficacy or safety), and C-QTc, typically based on CDISC ADaM / SDTM datasets. Prepare data for state-of-the-art NCA analysis, such as ADPC, PP, and ADPP, including the creation of defined packages and r

Full-time

Senior Statistical Programming Analyst - REMOTE ROLE

Remote

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2d ago

Description: Location: Remote, all time zones welcome! Key Responsibilities: Develop and maintain SAS programs for clinical and real-world data analysis. Work with CDISC standards (SDTM, ADaM) experience is a major plus. Perform PASR reporting and/or IJ analysis as needed. Analyze real-world insurance files, registry data, and post-market trial registry datasets. Collaborate with CROs, Sponsors, and cross-functional teams to ensure data integrity and compliance. Deliver accurate, timely outputs

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Contract

$65 - $70

Veeva Clinical Database Programmer

Remote or Hybrid in Thousand Oaks, California

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Today

Client: global biotech company Location:100% Remote from anywhere in the US Duration: 1 year + extensionsWe are seeking an experienced Veeva Clinical Database Programmer with strong expertise in clinical data standards to join our Biomedical Data Stewardship team. This role is responsible for contributing to the design of clinical trial databases within Veeva Clinical Data Management System (CDMS), ensuring compliance with internal data collection standards and supporting high-quality data entry

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Contract

BASED ON EXPERIENCE

Director, R&D Data Science, Data Products - Global Development

Remote or Hopewell Township, New Jersey

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Today

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

Full-time

USD 161,000.00 - 276,000.00 per year

Senior Programming Lead, Integrated Data Analytics and Reporting

Remote or Raritan, New Jersey

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Today

Full-time

USD 109,000.00 - 174,800.00 per year

Senior Real-World Data Architect

Remote

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Today

Type of Requisition: Regular Clearance Level Must Currently Possess: None Clearance Level Must Be Able to Obtain: None Public Trust/Other Required: None Job Family: Data Science and Data Engineering Job Qualifications: Skills: Cloud Applications, Cloud Solutions, Data Management, Data Science, Dataset Management Certifications: None Experience: 10 + years of related experience ship Required: No Job Description: GDIT is seeking an experienced Real-World Data Architect for upcoming opportu

Full-time

USD 198,050.00 - 267,950.00 per year

Health IT Consultant

Remote

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3d ago

Vector Consulting is looking for an experienced Health IT Consultant on a remote 9+ months (part-time) renewable Government contract inSilver Spring, MD. Position:Health IT Consultant This individual will work across various clinical projects across the agency supporting the responsibilities below: Participating as a subject matter expert for any clinical safety studies, respectively, which are submitted to the agency in support of drug applications. Reviewing clinical data for regulatory comp

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Contract

Depends on Experience

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CDISC jobs in Philadelphia, PA, USA