Junior Clinical Analyst Jobs

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Clinical Data Manager

Tandym Tech

•

Remote

Contract

A recognized pharmaceutical company has a great Remote opportunity awaiting a new Clinical Data Manager. In this role, the Clinical Data Manager will be responsible for contributing Data Management Support for assigned programs. The contractor is a self-motivated, collaborative clinical data management professional who is a self-starter and thrives in a fast-paced environment. Responsibilities: Work with the Clinical Data Management (CDM) Lead to support operational activities for one or more pr
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Posted 5 days ago | Updated 7 hours ago

Clinical Research Associate

Zachary Piper Solutions, LLC

•

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 43 days ago | Updated 4 hours ago

Hospital Clinical Program Manager - clinical in hospital inpatient setting.

APN Software Services, Inc

•

Newport Beach, California, USA

Full-time

Please contact Abdul on "" OR email me at "" 2 Openings for Quality Management Team - Roles are very specific - candidates must have in-depth experience in Clinical Quality Improvement in a hospital inpatient setting. Contract to Hire / Direct Hire opportunities for the right talent. 100% Onsite *Candidates must possess all 4 of the below or they will not be considered: 1. Completed PI training and certification (six sigma, lean, CPHQ, Masters in Improvement) from nationally recognized organiza
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Posted 7 days ago | Updated 1 day 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 43 days ago | Updated 4 hours ago

Clinical Research Assistant

Zachary Piper Solutions, LLC

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Bethesda, Maryland, USA

Full-time

Piper Clinical Solutions is seeking a Clinical Research Assistant in the Bethesda, MD area to support a well-established clinical research organization (CRO) focused on providing biopharmaceutical development support, health information services, and health & environment assessments to commercial and government clients. Responsibilities of the Clinical Research Assistant include: Assist in overall project support to various clinical research studies, with a specific focus in medical writing Rev
Posted 5 days ago | Updated 4 hours ago

Clinical Research Associate (CRA)

Zachary Piper Solutions, LLC

•

Remote

Full-time

Piper Companies is seeking a Clinical Research Associate (CRA) with experience in Oncology clinical trials to join a reputable clinical research organization. This is a full-time/permanent opportunity. Some travel is required (regionally, about 8-10 days out of the month). Candidates must be located in CST or PST in one of the following states: WY, CO, KS, WI, IN, OH, MN, MO, IL, MI, KY, AR, CA, OR, WA, NV, UT, AZ. Responsibilities of the Senior Clinical Research Associate (CRA): Perform site s
Posted 12 days ago | Updated 4 hours ago

Clinical Solutions Associate

HAYS

•

Raleigh, West Virginia, USA

Contract

Clinical Solutions Associate - Contract - Raleigh, NC - $70.00 - $70.00/hr. The final salary or hourly wage, as applicable, paid to each candidate/applicant for this position is ultimately dependent on a variety of factors, including, but not limited to, the candidate's/applicant's qualifications, skills, and level of experience as well as the geographical location of the position. Applicants must be legally authorized to work in the United States. Sponsorship not available. Our client is see
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Posted 3 hours ago

Clinical Application Support

Beacon Hill

•

Philadelphia, Pennsylvania, USA

Full-time

Location: Philadelphia, PA (4 days on site, 1 day remote) Salary: 75-80K We are seeking an Application Support Specialist with clinical industry experience to provide comprehensive technical support for clinical devices and applications. This role requires strong knowledge of clinical systems, field support, clinical data management, and configuration management. You will work closely with cross-functional teams to troubleshoot, resolve, and optimize clinical applications and devices to ensure
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Posted 14 days ago | Updated 7 hours ago

Clinical Research Associate

Zachary Piper Solutions, LLC

•

Remote

Full-time

Piper Companies is seeking a Clinical Research Associate (CRA) with experience in Oncology clinical trials to join a reputable clinical research organization. This is a full-time/permanent opportunity. Some travel is required (regionally, about 8-10 days out of the month). Candidates must be located in CST or PST in one of the following states: WY, CO, KS, WI, IN, OH, MN, MO, IL, MI, KY, AR, CA, OR, WA, NV, UT, AZ. Responsibilities of the Senior Clinical Research Associate (CRA): Perform site s
Posted 29 days ago | Updated 4 hours ago

Clinical Business Operations Associate

Informatic Technologies

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Remote

Contract

One of our leading Pharmaceutical client is looking to hire a Clinical Business Operations Associate in Morristown, NJ. Position Summary: The role of the Clinical Business Operations Associate is to review and approve invoices and expenses against contracts established with the Research and Development function of Clinical Operations globally. Additionally, support and manage a variety of clinical contracts, various contract administrative and legal matters as needed. This role can work from Cli
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Posted 12 days ago | Updated 9 hours ago

Clinical Pharmacologist

Sunrise Systems, Inc.

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Remote

Contract

Job Title: Clinical Pharmacologist Job ID: 25-07547 Location: 100% REMOTE Duration: 06 months on W2 Contract Description: Director, Clinical Pharmacology Virtual(via Kendall Square, Cambridge, MA) This contractor will serve as a back up to the internal FTE on projects. This individual will support the PK/PD aspects of clinical studies (from protocol to CSR) and related regulatory submission activities. This role requires a strong pharmacokinetics/pharmacodynamics/pharmacometrics knowledge.
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Posted 36 days ago | Updated 14 hours ago

Program Manager with healthcare, med-tech, or optometry/clinical workflow knowledge.

Valueprosite

•

Dallas, Texas, USA

Third Party, Contract

Candidates must be local to Dallas, TX. Candidate profiles should align closely with the Optometry & Key Account Partnerships role. Here's the brief JD they should match: Strong project ownership and strategic planning experience. Proven executive engagement skills, working with C-level stakeholders. Cross-functional leadership across business, IT, operations teams. Strong background in risk management, compliance, and quality assurance. Excellent reporting and executive-ready communication skil
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Posted 1 day ago | Updated 14 hours ago

SAS Clinical Trails Programmer

Katalyst Healthcares and Lifesciences

•

Cary, North Carolina, USA

Full-time

Responsibilities: The consultant will provide programming/analytical support utilizing client as the primary programming language to create and manage the production of analysis reports. summary tables/listings and graphs for clinical trials submitted to various regulatory bodies worldwide. The consultant must have excellent communication skills and must be able to communicate about the techniques developed and results of analysis both to executives and other analysts in the organization. Pe
Posted 7 hours ago

Data Engineer (SQL, Python, AI/ML, Snowflake, biostatistics, clinical trial, Imaging)

Diligente Technologies

•

Sunnyvale, California, USA

Contract

Summary: We re seeking a Data Engineer with strong SQL and Python skills to build and maintain data pipelines supporting clinical enrolment analytics. You ll work closely with data scientists and analysts to ensure clean, scalable, and reliable data systems. Note: Background in clinical trials, biostatistics, Imaging, or healthcare data is must have. PRINCIPAL RESPONSIBILITIES: Must-Have Skills: Advanced SQL and Python (data manipulation, ETL/ELT).Strong understanding of data engineering best pr
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Posted 8 days ago

Director 2, Clinical Engineering - G

Next Step Systems

•

Zanesville, Ohio, USA

Full-time

Director 2, Clinical Engineering We are seeking an experienced individual for a Director 2, Clinical Engineering opening in Zanesville, OH. The Director 2, Clinical Engineering will oversee numerous types of medical equipment, offer hands-on experience, and provide leadership and process-improvement knowledge to staff. The Director 2, Clinical Engineering should be a high-level leader that can manage a team of supervisors and technical professionals. This is a fantastic opportunity for any acco
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Posted 8 days ago | Updated 10 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 7 hours ago

Senior Consultant - Clinical Data Programming

Veeva Systems

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Raleigh, North Carolina, USA

Full-time

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company - we made history in 2021 by becoming a public benefit corporation
Posted 4 days ago | Updated 6 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Irving, Texas, USA

Full-time

Responsibilities: Performing data manipulation, analysis, and reporting of clinical trial data for both safety and efficacy (ISS/Client) utilizing SAS programming. Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs). Production and QC / validation programming. Ability to program from scratch and able to handle complicated domains and TLF's. Ability to read and apply protocol and SAP. Demonstrate good understanding of the endpoints and d
Posted 7 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

San Diego, California, USA

Full-time

Responsibilities: Manage programming activities on project or study level, including managing CROs to ensure deliverables are accurate and compliant. Act as a Programming SME for assigned studies, including authoring/reviewing programming specifications, such as SDTM/ADaM specifications, TFLs creation and QC for reporting events, ESUB packages, and documenting production and validation programs. Apply programming skills to support statistical analysis, clinical reporting, regulatory submission
Posted 7 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Boston, Massachusetts, USA

Full-time

Responsibilities: Attending multi-disciplinary team meetings, representing the programming function. 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. Develop software systems to generate displays of clinal all stu
Posted 7 hours ago