Entry Level Clinical Data Manager Jobs

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Senior Clinical Data Analyst

Katalyst Healthcares and Lifesciences

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

Clinical Data Analyst

Katalyst Healthcares and Lifesciences

Irvine, California, USA

Full-time

Responsibilities: The main function of a clinical data analyst is to create moderately complex metrics to identify trends in data and remediation, utilizing tools (e.g., systems, reports) to assess the need for training and provide basic recommendations to improve data status during study conduct. Evaluate data errors and collection issues; provide guidance and recommendations to the clinical team for resolution. Define and specify clinically data collection requirements (e.g., eCRFs, CRFs, ed

Clinical Research Coordinator

Zachary Piper Solutions, LLC

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

Clinical Research Coordinator

Zachary Piper Solutions, LLC

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

Clinical Research Engineer III - Onsite Role

Prospance Inc.

Mountain View, California, USA

Contract

Work closely with clinical research scientists, associates, and other team members to design and execute clinical studiesProvide data monitoring tools and data analysis toolsCreates tools to streamline data processesAuthors tool qualification reportsMonitors study datasets to main high data qualityAnalyzes signal quality of biosensor dataProvide support to clinical research organizations during planning and execution of clinical studiesPerforms clinical data analysis and provides statistical inf

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

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Athens, Georgia, 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

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

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

Clinical Business Systems Analyst - D/T NYC, onsite

Winston Staffing Service

New York, New York, USA

Contract

A clinical business analyst plays a crucial role in healthcare organizations by analyzing clinical data and operations to improve business performance and ensure regulatory compliance. Duties & Responsibilities Analyze and document business requirements and processes; communicate requirements to technical personnel through the construction of basic conceptual data, process models and flowcharts, and technical specifications.Interview end users, stakeholders, and project sponsors in order to ass

Clinical Review Nurse - Concurrent Review

Pyramid Consulting, Inc.

Remote

Contract

Immediate need for a talented Clinical Review Nurse - Concurrent Review. This is a 06+months contract opportunity with long-term potential and is located in TX(Remote). Please review the job description below and contact me ASAP if you are interested. Job ID: 25-78309 Pay Range: $33 - $39/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Performs concurrent rev

RN Clinical Nurse

Pyramid Consulting, Inc.

Atlanta, Georgia, USA

Full-time

Immediate need for a talented RN Clinical Nurse. This is a Fulltime opportunity with long-term potential and is located in Atlanta, GA (Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID:25-77207 Pay Range: $82000 - $90000/annum. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Exemplary Practice and Outcomes.Perform

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

Clinical Documentation SpecialistCDIin California

Pyramid Consulting, Inc.

Remote

Contract

Immediate need for a talented Clinical Documentation Specialist CDI in California. This is a 06+months contract opportunity with long-term potential and is located in California(REMOTE). Please review the job description below and contact me ASAP if you are interested. Job ID: 25-77657 Pay Range: $45 - $50/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Effec

Remote Veeva Clinical Business Analyst

Dale Workforce Solutions

Remote or Princeton, New Jersey, USA

Contract

Analysts for Veeva Vault implementations help guide our clients in the configuration and deployment of Veeva s cloud-based solutions, ensuring successful outcomes for any and all aspects of the project. A successful analyst should be well-versed in translating design documents into functional specifications, mapping business processes for technical solutions, and documenting business requirements for the core application, system integrations, and legacy data/document migrations. The analyst is a

Clinical Systems Specialist

Tandym Tech

Woburn, Massachusetts, USA

Contract

A biotech company in Massachusetts has a great Remote contract opportunity awaiting a new Clinical Systems Specialist. In this role, the Clinical Systems Specialist will be responsible for supporting the lifecycle management of clinical systems for Global Development Operations. To be considered for this opportunity, the qualified professional must be able to work on a W2 basis. Responsibilities: Work on planning, design, configuration, and deployment of new clinical systems and enhancements

Senior Clinical Java Architect

Tror

Eden Prairie, Minnesota, USA

Contract, Third Party

Position: Senior Clinical Java Architect Location: Eden Prairie, Minnesota (Hybrid 3 days onsite) Duration: 6+ months Contract: C2C/w2 Job Description: Seeking a highly experienced Clinical Java Architect with a strong background in designing and implementing complex, high-availability clinical systems in healthcare settings. This role demands deep expertise in Java-based backend architectures, along with hands-on knowledge of healthcare data standards (e.g., HL7, FHIR, CCD, DICOM) and int

Clinical Project Manager

Info Way Solutions

New York, New York, USA

Third Party, Contract

Clinical R&D + Project management Comfortable working in a matrix environment with clinical, regulatory, and tech teams.Demonstrates strong problem-solving and decision-making under tight timelines.Ability to lead and coordinate cross-functional teams from offshore and onshore.Strong stakeholder management and communication across time zones and geographies.Proactively identify opportunities for process automationSkilled at translating business needs into technical project requirements.Ability t

Clinical Supply Chain Specialist

NexInfo Solutions, Inc.

Foster City, California, USA

Contract, Third Party

About Nexinfo: NexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors. They offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions. The company aims to help businesses across industries achieve their goals through industry best practices, lean process design, and advanced software solutions. Their ERP-related services address challenges

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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