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Clinical Data manager

Intone Networks Inc.

•

Remote

Third Party, Contract

Need stronger with working on Data Acquisition, DTAs and vendor relations. Responsibilities: Support the planning, setup, and acquisition of external clinical data at the study level, assisting in managing study start-up, conduct, and closeout activities.Assist in creating external data transfer agreements, ensuring alignment with Takeda Standards and specifications to support data integration, analysis, and reporting.Provide support in setting up infrastructure for external data to flow into T
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Posted 26 days ago | Updated 20 days ago

Clinical Data Specialist

Katalyst Healthcares and Lifesciences

•

Illinois, USA

Full-time

Responsibilities: Reporting to the Clinical Data Manager, you'll be responsible for the development of real-world data variables from structured and unstructured data sources, including designing data capture forms and supplemental procedures to instruct the abstraction process. You'll lead the execution of feasibility testing to de-risk data capture approaches and own the implementation of data validation checks to ensure data quality. In addition, you'll work alongside other team members on
Posted 31 days ago | Updated 2 hours ago

Clinical Data Specialist

Katalyst Healthcares and Lifesciences

•

San Diego, California, USA

Full-time

Responsibilities: Reporting to the Clinical Data Manager, you'll be responsible for the development of real-world data variables from structured and unstructured data sources, including designing data capture forms and supplemental procedures to instruct the abstraction process. You'll lead the execution of feasibility testing to de-risk data capture approaches, and own the implementation of data validation checks to ensure data quality. In addition, you'll work alongside other team members o
Posted 10 days ago | Updated 2 hours ago

Clinical Business/Data Analyst - NYC (onsite)

Winston Staffing Service

•

New York, New York, USA

Contract

This position requires onsite, 5 days a week, Monday Friday in Downtown, NYC. This Role will be 100% on site with potential to hire. If hired, it will be 2 days at home and 3 days in office. Interviews will be Virtual and only PREA required. Previous experience working with Clinical Data a must **NO AGENCIES, NO EMPLOYERS, NO 1099, NO C2C Must have year of experience gathering and documenting business, clinical, and/or functional requirements for software applications development and implement
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Posted 28 days ago | Updated 14 days ago

Clinical Laboratory Scientist II (CLS) -Generalist

Power Personnel

•

San Jose, California, USA

Full-time

Job DescriptionJob Description Here is the enhanced and refined job description for the Clinical Laboratory Scientist II (CLS) - Generalist position: Elevator PitchAre you a Clinical Laboratory Scientist and want to gain experience at one of the nation's top teaching Hospitals? Join now! Want to gain world-leading experience in CLS? Join now! About the Job Pay Rate: $105.00Location: 225 N Jackson Avenue, San Jose, CA 95116Schedule: 5 days a week, alternating weekendsShift details: 11:00pm-7:30
Posted 7 days ago | Updated 1 hour ago

Clinical User Experience and Endpoint Lead

Innova Solutions, Inc

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Fredericton, New Brunswick, Canada

Contract

A client of Innova Solutions is immediately hiring for a Clinical User Experience and Endpoint Lead. Position type: Contract Location: Fredericton, New Brunswick, Canada As a Clinical User Experience and Endpoint Lead, you will be responsible for: Description: A Bachelor s level University degree in Computer Science, Business Administration, Healthcare or a similar discipline.Demonstrated experience in a user experience leadership role on at least one major Clinical Information System implemen
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Posted 9 days ago

Clinical EMR Systems Analyst

Vaco by Highspring

•

Columbus, Ohio, USA

Full-time

Direct Hire - Local to Columbus, OH Cannot provide Sponsorship at this time Compensation $60,000 - $70,000 dependent upon experience The Senior Clinical Systems Analyst serves as the lead implementation and support person for all clinical applications and facilitates the configuration, implementation, and training of the electronic medical record and other clinical computer software. The Senior Clinical Systems Analyst is a subject matter expert assisting in the resolution of issues affecting a
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Posted 9 days ago

Clinical Editing Coding Analyst | Remote | Contract

Walker Healthforce

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Remote

Contract

Clinical Editing Coding Analyst |Remote |Contract Walker Healthforce is seeking a Clinical Editing Coding Analyst with 1-5+ years of experience.. This is a 6-month contract opportunity. CORE REQUIREMENTS: Certified Professional Codercertification (e.g., CPC, CCS, CCS-P, or RHIT) 1-5 years experience - in billing/coding (preferably in a comprehensive surgical center or facility) or Claims resolution (including adjudication, coding, thorough analysis and problem-solving) Ability to analyze, inves
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Posted 28 days ago | Updated 19 days ago

Sr. Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Newark, New Jersey, 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. Fulfill ad-hoc analysis requests. Provide other services. Requirements: Ba
Posted 27 days ago | Updated 1 hour ago

B2B Healthcare/Clinical Solutions Product Marketing Manager

U.S. Tech Solutions Inc.

•

San Bruno, California, USA

Contract

Job Description: We are looking for a creative, analytical, and detail-oriented Product Marketing Associate to join our growing team.This role is ideal for someone with a background in strategy consulting or product marketing, particularly in the healthcare, life sciences, or pharmaceutical industries.The successful candidate will play a key role in creating high-impact presentation materials that support strategic commercial opportunities across client diverse product portfolio.Reporting to the
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Posted 19 days ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Chicago, Illinois, USA

Full-time

Responsibilities: Create or review and approve programming plans at study and project level. Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.) Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies. Attending multi-disciplinary team meetings, representing the programming function. Develop software systems to generate displays of clinal al study
Posted 13 days ago | Updated 2 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Cambridge, Massachusetts, USA

Full-time

Responsibilities: Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.). Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies. Develop software systems to generate displays of clinal al study data as tables, listings, and graphs for electronic submission to regulatory agencies. Attending multi-disciplinary team meetings, representing the programmi
Posted 19 days ago | Updated 13 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Newark, 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 17 days ago | Updated 2 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

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 32 days ago | Updated 2 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Austin, Texas, 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 5 days ago | Updated 2 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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Minneapolis, Minnesota, 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 20 days ago | Updated 2 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Hartford, Connecticut, 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 10 days ago | Updated 2 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Boulder, Colorado, USA

Full-time

Responsibilities: Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget. Conduct hands-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results for internal and external audiences. Ensure all relevant deliverables including investigator brochures, publications, all regulatory submission
Posted 13 days ago | Updated 13 hours ago

Clinical Supply Systems Administrator

Johnson & Johnson

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Remote or Malvern, Pennsylvania, USA

Full-time

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
Posted 3 days ago | Updated 2 hours ago

Senior Clinical Data Analyst

Katalyst Healthcares and Lifesciences

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Boston, Massachusetts, USA

Full-time

Job Description: This position focuses on assisting with analysing data and deriving insights from clinical and safety data sources to generate evidence and support decision making across the organization. The Associate will leverage a variety of analytics and visualization techniques to contribute to research, clinical development, drug safety and post-marketing activities. Responsibilities: Collaborates and works closely with cross-functional teams, including data analysts/engineers and busin
Posted 60+ days ago | Updated 1 hour ago