Research Analyst

• Performs standardized research and evaluation activities under leadership supervision, including developing project materials, coordinating data collection activities, and supporting dissemination.
• Performs standardized support tasks for research and evaluation activities, including organizing project materials, taking meeting minutes, and keeping logs of compliance related documents.
• Conducts supervised data collection, which could include surveys, interviews, field observations, site visits and focus groups.
• Contributes to analysis and reporting under leadership supervision; may include quantitative and qualitative data and data visualization techniques.

Research Associate I

• Conducting thorough research into an individuals’ background using a variety of tools, such as databases and public records
• Gathering information, analyzing data, and compiling this information to be entered into a final report
• Processing searches related to background screening reports
• Ensuring all searches are processed and reported according to state and federal laws as outlined in AccuSourceHR’s reporting guidelines
• Ensuring all searches are processed according to client guidelines
• Retrieving public records information and entering said information into our platform
• Analyzing information and comparing data sets to confirm matching identifiers
• Performing other duties as assigned
• Meeting or exceeding minimum standard service requirements

Research Specialist

• Performs standardized research and evaluation activities with minimal oversight, including developing project materials and supporting dissemination.
• Performs standardized support tasks for research and evaluation activities, including organizing project materials, taking meeting minutes, and keeping logs of compliance related documents.
• Contributes to analysis and reporting with minimal oversight; may include quantitative and qualitative data and data visualization techniques.
• Serves as task lead or project manager, including maintaining project plan, timeline, and deliverable schedule.
• Conducts (and may lead some aspects of) data collection, which could include surveys, interviews, field observations, site visits and focus groups.

Research Associate II

• Provides high quality customer service to merchants by responding to inquiries regarding the support of Merchant Credit Card processing as well as other areas as assigned
• Responds to telephone inquiries, requests and problems from merchants
• Troubleshoots, diagnoses and provides merchants with solutions to resolve problems with service, authorization and credit card processing terminals
• Communicates applicable policies, procedures and practices to merchants
• Requests exceptions to policies and procedures on behalf of merchant as appropriate, within established limits

• Identify, develop, and implement solutions to improve accuracy and integrity of claims payments across the Plan.
• Scope PI initiatives and analyze claims data.
• Develop implementation assessment plans and collaborate with internal and external stakeholders.
• Optimize payment processes by leveraging understanding of Providence Health Plan infrastructure and related functions.

Research Analyst – Medical Management

• Oversee the management and tracking of clinical trial data to ensure accuracy, integrity, and completeness.
• Conduct site qualification visits, site monitoring visits, and study close-out visits. Provide support to site staff during audits or inspections.
• Ensure clinical trials are conducted in compliance with protocols, Good Clinical Practice (GCP), ICH guidelines, SOPs, and regulatory standards (FDA/DEA).
• Review and manage electronic Case Report Forms (eCRFs), ensuring data is accurate and aligned with study protocols.
• Assist in the development and maintenance of Case Report Forms (CRFs) and other study-related documents.
• Provide training to site personnel on study procedures, protocols, and regulatory requirements.
• Regularly review data entered into the Electronic Data Capture (EDC) system to ensure compliance with study protocols.
• Identify, address, and escalate any study-related risks, issues, or opportunities for improvements.
• Follow up with clinical sites to ensure that data collection is progressing as planned and all required documentation is completed.
• Ensure timely and accurate management of regulatory documents and maintain compliance with regulatory requirements.
• Engage with Key Opinion Leaders (KOLs) in the medical and research communities to stay informed on scientific research and clinical data.
• Stay up-to-date with the latest developments in scientific research and clinical data relevant to Kuros Biosciences.
• Review and track clinical trial-related invoices, ensuring accuracy and compliance.
• Contribute to the creation and maintenance of project plans for clinical trials, ensuring alignment with company policies and timelines.
• Work independently to complete tasks while ensuring alignment with team objectives, timelines, and expectations.
• Expected to travel 3-5 days per month for site visits and clinical trial support.

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Research Associate I

Research Specialist

Research Associate II

Research Analyst

Research Analyst – Medical Management

Clinical Research Associate