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• Manage administration of the Rave URL activities: Report Administration, eLearning, User Roles and Core Configuration.
• Lead development of study database, including programming of clinical database according to CRF Specifications.
• Support global library by programming forms and edit checks according to data collection standards.

Jobgether is a platform that uses AI to match candidates with jobs, ensuring a quick and fair review process. They provide a supportive team culture and collaboration.

The Senior Manager of Clinical Data Management (CDM) is responsible for overseeing the execution, quality, and operational excellence of data management activities across Phase IV, post-marketing, and real-world evidence (RWE) studies. Plays a key role in shaping data delivery strategy, driving cross-functional collaboration, and ensuring consistent, high-quality outcomes across a growing portfolio. Requires strong technical expertise, exceptional leadership capability, and the ability to operate strategically while maintaining hands-on oversight of complex data workflows.

Paradigm is rebuilding the clinical research ecosystem by enabling equitable access to trials for all patients.

• Remote-first QA of clinical text and structured EHR data.
• Localized to Chicago.
• Requires careful judgment, consistent annotation quality, and attention to detail in complex datasets.

Alignerr is a recruiting company. They're looking for a Clinical Data QA Reviewer.

Performs cancer registry duties related to completion of abstracts for benign and malignant processes for the cancer database. Complies with the established standards of Commission on Cancer, Georgia Cancer Registry, and the Piedmont Cancer Committee. This is a remote position.

Join Piedmont to move your career in the right direction and be recognized for your contributions to exceptional patient outcomes.

Deliver high-quality product presentations to family physicians and clinic groups across Canada. Adapt your message to the specific needs of each clinic or group practice. Partner closely with Sales Development Representatives to convert qualified opportunities into new customers.

MEDFAR Clinical Solutions was founded in 2010 and was the first company to certify a cloud-based Electronic Medical Record in Canada: MYLE.

• Lead complex clinical trials from initiation through completion.
• Oversee cross-functional teams and manage project scope.
• Contribute to high-impact clinical research projects.

This position is posted by Jobgether on behalf of a partner company.

Manage, analyze, and transform complex biomedical and clinical data to support research and decision-making. Implement robust data pipelines, quality control procedures, and reporting tools. Collaborate with cross-functional teams to design data collection instruments and develop dashboards.

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements.

• Monitoring and maintaining data quality by validating, cleansing, and enriching data as needed.
• Creating and maintaining data dictionaries, data lineage, and metadata management practices.
• Training end-users on data management best practices and procedures.

Precision Medicine Group is an Equal Opportunity Employer.

The data analyst is focused on determining and developing reporting of major business drivers. Responsible for coordinating and facilitating the Data Governance workgroup. Providing data support to various management staff and groups, including the Management Team, Health Care Delivery teams, External Affairs teams, CEO, and CFO.

Planned Parenthood of Northern New England was founded on the belief that everyone has the fundamental right to make decisions about their bodies.

The Data Integrity Analyst will monitor and ensure accuracy and reliability of data. This role is responsible for data validation between systems and translating business requirements into technical specifications, as well as developing data warehousing and modeling standards. They will contribute to data loading and/or validation in an order management system and an ERP.

KnipperHEALTH's passion, actions, and focus is their strength, and they invite you to become one of their contributors to the team.

• Monitor and own the progress of clinical studies at investigative sites.
• Coordinate all necessary activities required to set up and monitor a study.
• Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.

Precision for Medicine integrates clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences to improve the speed, cost and success rate of bringing life-changing therapies to patients. They have a strong focus on Oncology and Rare Disease and boast extremely high CRA retention rates compared to industry averages.

• Lead the full credentialing lifecycle for new and existing providers and practice locations including Medicare and Medicare Advantage plans.
• Ensure CAQH profiles are complete, current, and accurately reflect provider credentials and practice information.
• Assess current credentialing processes, identify inefficiencies, and implement improvements using Airtable, automation tools, and best practices.

Sailor Health is on a mission to solve the mental health crisis among older adults, building the platform for senior mental health.

As Clinical Trial Manager, you will lead CRAs and oversee clinical aspects of studies across multiple countries. You will ensure timeline adherence and scope, whilst ensuring quality delivery. Management and operational delivery of the clinical elements within a trial including site selection, start-up, and data cleaning activities. Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor.

Precision for Medicine is a precision medicine CRO which combines novel clinical trial designs, experts and biomarker solutions.

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.

ICON plc is a world-leading healthcare intelligence and clinical research organization. ICON fosters an inclusive environment driving innovation and excellence.

• Provide full support to colleagues from other areas in the company, specifically Sales and Account Management.
• Set up and processing merge/purge campaign using Adstra merge processes and communicate merge results to internal stakeholders.
• QC, format, and ‘map’ data files and process all data through NCOA (National Change of Address) service.

Adstra provides a comprehensive suite of data and identity solutions for a wide-array of use cases to a diverse base of blue-chip clients.

Strengthen relationships with Jane’s largest clinics through proactive outreach. Drive retention and feature adoption by helping clinics understand and leverage Jane’s capabilities. Influence Jane’s product direction by bringing forward clear, customer-informed insights and trends.

Jane is a high growth SaaS company that builds the products and tools that thousands of clinics rely on every day to run their businesses and care for their patients.

• Assists with the build of the NPM clinical platform
• Develops work instructions and data guides to support variable sets built for the NPM platform
• Works with our team of data engineers, clinical subject matter experts and other staff to support development and implement quality data variables

N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials.

• Analyze and implement streamlined processes for the GTM team.
• Manage data integrity within CRM and other sales tools.
• Develop and maintain dashboards to track key prospecting and pipeline performance metrics.

Motive empowers the people who run physical operations with tools to make their work safer, more productive, and more profitable.

• Monitor and own the progress of clinical studies at investigative sites.
• Coordinate activities to set up and monitor a study.
• Train and mentor junior staff members.

Precision for Medicine integrates clinical trial execution with scientific knowledge, laboratory expertise, and data sciences to improve the success rate of therapies for patients. They cultivate their culture and have high CRA retention rates compared to industry averages.

• Provide support, direction, and technical assistance to CDI staff.
• Manage staffing needs by identifying needs and collaborating with Staffing Teams.
• Monitor productivity, quality, and utilization levels within the CDI team.

UASI provides a supportive environment that encourages professional development and enables each employee to achieve their individual goals.