Clinical Psychologist - Presque Isle ME Jobs

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Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

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 51 days ago | Updated 11 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

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 31 days ago | Updated 11 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Boulder, Colorado, 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 47 days ago | Updated 11 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Omaha, Nebraska, 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 26 days ago | Updated 11 hours ago

IT Service Desk Clinical

JConnect Inc

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Salt Lake City, Utah, USA

Full-time

Strong problem-solving and troubleshooting skills - Ability to identify and triage issues related to the Epic system, and if required resolve them. Excellent communication and interpersonal skills: Ability to collaborate with diverse teams and effectively communicate technical information. Experience in Service Desk ITIL practices and working knowledge on ServiceNow ITSM tool Understanding of EPIC EHR system preferable, not necessary - Knowledge of specific modules relevant to the role (e.g.,
Easy Apply
Posted 12 days ago | Updated 5 hours ago

Clinical Data manager

Intone Networks Inc.

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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
Easy Apply
Posted 25 days ago | Updated 20 days ago

Clinical Laboratory Scientist II (CLS) -Generalist

Power Personnel

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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 10 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 11 hours ago

Clinical Data Specialist

Katalyst Healthcares and Lifesciences

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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 11 hours ago

Clinical Business/Data Analyst - NYC (onsite)

Winston Staffing Service

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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
Easy Apply
Posted 28 days ago | Updated 14 days 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
Easy Apply
Posted 9 days ago

Clinical EMR Systems Analyst

Vaco by Highspring

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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
Easy Apply
Posted 28 days ago | Updated 19 days ago

Sr. Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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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 11 hours 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
Easy Apply
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 11 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 11 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 23 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 11 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 11 hours ago