Clinical trials Jobs

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Statistical Programmer (Clinical Trials)

Ledgent Technology

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Remote

Contract

We are seeking a Statistical Programmer to work on a remote team for a project with our client. The preferred R stack experience includes dplyr, rmarkdown, dbplyr, ggplot2, roxygen, and plotly to solve complex challenge. We are unable to work with 3rd party candidates. Summary The main function of Sr. Analyst is to develop, validate datasets, tables/listing/figures using SAS/R programming language, and other ad-hoc request to support business requirements. Job Responsibilities *In this rol
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Posted 18 days ago | Updated 7 hours ago

Sr. Principal Statistics

PARAKEET WORLD SOLUTIONS LLC

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Remote

Contract

Job Title: Sr. Principal StatisticsLocation: Remote Duration: 6 MonthsEmployment Type: W2 ContractExperience Level: Mid-SeniorEducation Required: Ph.D. or MS in Statistics or BiostatisticsIndustry: Pharmaceuticals Job Summary:The Sr. Principal Statistician will lead statistical activities in clinical trials, from protocol development to final study reporting. The role will also contribute to regulatory filings, in-licensing evaluations, and marketing support. Key Responsibilities:Review protocol
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Posted 7 days ago

eClinical Project Manager

Biogensys

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Remote

Contract

Title: eClinical Project Manager Duration: Long term Contract Location: NJ/NY- Remote option available Rate: Flexible Required skills: Proven experience managing eClinical or eCOA product implementations.Own the end-to-end delivery of eClinical initiatives, including eCOA platform rollouts, device provisioning, and integration with client systemsFamiliarity with device provisioning workflows and mobile device managementStrong understanding of clinical trial operations, regulatory compliance, and
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Posted 5 days ago

RN - HIV Medicine Office

Albany Medical Center

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Albany, New York, USA

Full-time

Job DescriptionDepartment/Unit: HBD - Aids Program Work Shift: Day (United States of America) Salary Range: $60,028.00 - $99,023.00 Registered Nurse (RN) Full time HIV Medicine Clinic - Albany, NY We have an exciting part time opportunity for a caring and compassionate RN to join our HIV Medicine Clinic team of dedicated healthcare providers! The Albany Medical College Division of HIV Medicine (DHIVM) offers comprehensive HIV services including primary medical care, medical case management,
Posted 35 days ago | Updated 6 hours ago

Clinical Research Associate

Zachary Piper Solutions, LLC

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Sacramento, California, USA

Full-time

Piper Companies is currently seeking an Oncology Clinical Research Associate (CRA) for an opportunity in Sacramento, California (CA). The Oncology Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Oncology Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monito
Posted 60+ days ago | Updated 28 days ago

Senior Sourcing Manager*

Cube Hub, Inc.

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California, USA

Contract

Description: True Job Title: R&D Sourcing Manager Location: Prefer Foster City, but can be remote in the US The R&D Sourcing Manager will be responsible for sourcing and contracting development organizations to support client global Phase I IV clinical trials, as well as other ad hoc projects within the Vendor Outsourcing department. This role will primarily focus on clinical ancillary services and systems used across development. Familiarity with technology, systems, and software is a plus,
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Posted 7 days ago | Updated 1 hour ago

Development Engineer 3

Katalyst Healthcares and Lifesciences

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Santa Clara, California, USA

Full-time

Job Description: The Medical Imaging Specialist is responsible for providing CT and MR imaging expertise for the Intuitive 3D modelling service and operation team. This includes performing initial inspection of CT and MR scans received for 3D model segmentation, providing in-process consultation for segmentation technicians, and performing final QC for segmented 3D models to ensure delivery of high-quality 3D models to customers for use in patient education, pre-operative planning and intra-ope
Posted 18 days ago | Updated 6 hours ago

Clinical Research Associate

Zachary Piper Solutions, LLC

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Los Angeles, California, USA

Full-time

Piper Companies is currently seeking a Clinical Research Associate (CRA) for an opportunity in Los Angeles, California (CA). The Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monitoring and study activation
Posted 60+ days ago | Updated 28 days ago

Clinical Research Coordinator

Zachary Piper Solutions, LLC

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Raleigh, North Carolina, USA

Full-time

Piper Companies is seeking a highly organized and proactive Clinical Research Coordinator (CRC) to support clinical trials across multiple therapeutic areas on-site in the Raleigh, NC area. This role is essential in ensuring smooth trial execution within a clinical site network, with a focus on phlebotomy and patient coordination. Key Responsibilities of the Clinical Research Coordinator: Oversee day-to-day clinical trial activities while ensuring compliance with Google Cloud Platform, IRB, and
Posted 31 days ago | Updated 28 days ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Dallas, Texas, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p
Posted 2 days ago | Updated 6 hours ago

Clinical Research Coordinator

Zachary Piper Solutions, LLC

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Raleigh, North Carolina, USA

Full-time

Piper Companies is seeking a detail-oriented and proactive Clinical Research Coordinator (CRC) to join our growing clinical research team. The ideal candidate will have hands-on phlebotomy experience and a strong background working within a clinical site network environment. This role is essential in supporting the execution of clinical trials across multiple therapeutic areas. Responsibilities for the Clinical Research Coordinator: Coordinate and manage day-to-day clinical trial activities in
Posted 39 days ago | Updated 28 days ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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Princeton, New Jersey, USA

Full-time

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases.
Posted 3 days ago | Updated 6 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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Bridgewater, New Jersey, USA

Full-time

Responsibilities: Lead and participate in the development and validation of high quality CDISC datasets based on the implementation guides and consultations with sponsors, project leads, systems analysts, other programmers, and end users. Use your expertise in data standards and regulatory requirements to lead discussions with clients about appropriate approaches to database design. Use study protocol, CRF, Data Transfer Agreements from vendors, data sources, CDISC CT, TAUGS, and CDISC implement
Posted 60+ days ago | Updated 6 hours ago

Clinical Data Associate

Mayo Clinic

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Jacksonville, Florida, USA

Full-time

Job Description Under the direct supervision of the study team and research leadership, assists in coordinating the details of the study and documentation concerning study protocols, patient scheduling, retrospective & prospective chart work, data collection, data entry, data management, follow-up information, and compliance with federal, state, sponsor, and institutional guidelines. Overview for the Clinical Data Associate I: The CDA I provides data management support for clinical trials. The
Posted 2 days ago | Updated 6 hours ago

System Analyst - Healthcare

Pinnacle Software Solutions

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Cincinnati, Ohio, USA

Contract

Job Title: System Analyst - Healthcare (#9107-1) Location: Cincinnati, OH (On-site) Company: Tata Consultancy Services (TCS) Experience Level: Mid-Senior (7+ years) Education Level: Bachelor s Degree Job Description We are seeking a highly skilled and experienced System Analyst with expertise in healthcare systems and clinical trial systems. The ideal candidate will analyze, design, and implement innovative system solutions to support healthcare clients, ensuring the highest level of efficiency
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Posted 14 days ago | Updated 7 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Lake Success, New York, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p
Posted 22 days ago | Updated 6 hours ago

Sr. Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Indianapolis, Indiana, USA

Full-time

Responsibilities: Perform data manipulation, analysis, and reporting of clinical trial data. Develop and maintain department/system-level macros. Create and review SDTM and Adam specifications. Create and validate SDTM data sets. Create and validate analysis data sets. Create and validate patient profiles. Program and generate tables, figures, and listings (TFLs). Validate and document SAS programs and outputs. Fulfil ad-hoc analysis requests. Provide other services. Requirements: Bachelor's deg
Posted 49 days ago | Updated 6 hours ago

Clinical Safety Coder - MedDRA/WHODrug

General Dynamics Information Technology

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Maryland, USA

Full-time

Type of Requisition: Regular Clearance Level Must Currently Possess: None Clearance Level Must Be Able to Obtain: None Public Trust/Other Required: NACI (T1) Job Family: Medical Affairs Job Qualifications: Skills: Clinical Research, MedDRA, WHODrugCertifications: NoneExperience: 6 + years of related experienceship Required: Yes Job Description: GDIT's Military Health team is hiring a Clinical Safety Coder - MedDRA/WHODrug to support the Office of Regulated Activities (ORA) under the DoD (D
Posted 7 days ago | Updated 14 hours ago

SAS Programmer

Katalyst Healthcares and Lifesciences

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San Diego, California, USA

Full-time

Responsibilities: Serves as lead programmer for assigned projects to provide statistical and programming support in one or more Phase I- clinical studies. Design and perform quality checks on analysis datasets, tables, listings, figures (TFL), and written reports to support clinical trial results using SAS. Create and review annotated CRF to STDM datasets. Produce and maintain technical programming specification documents. Lead and actively participate in client and project review meetings.
Posted 53 days ago | Updated 6 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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South San Francisco, California, USA

Full-time

Responsibilities: Performs all SAS programming required for clinical trial analysis and reporting. Ensures that activities and processes performed are conducted according to sponsor requirements. Works closely with the Biostatistics and Data Management departments on various clinical projects. Designs and/or reviews database structure. Writes edit checks from the Data Cleaning Plan (DCP) specifications. Creates derived-analysis datasets. Executes analyses specified in the Statistical Anal
Posted 60+ days ago | Updated 6 hours ago