Research Analyst

• Play a support role on project teams while building your skills and experience.
• Work closely with project managers and senior staff to keep projects on track, provide responsive technical assistance to client partners, and contribute to high-quality deliverables.
• Take notes during project team meetings; summarizing and distributing the notes after the meeting; creating follow-up tasks for team members in our project management software.
• Work closely with the project lead to regularly review the project management plan, summarizing project status for the project lead, identifying areas for follow-up, and drafting team meeting agendas.
• Work closely with the project lead to draft client communications, meeting agendas, project invoicing status updates, and other communications.
• Provide proactive and responsive technical assistance (training, support, coaching through technical tasks related to our projects) to client partners that are aligned with project goals.
• Monitor process and outcome data to identify data quality concerns and support organizations in addressing emerging issues.
• Participate in technical assistance activities by providing logistical support for trainings, preparing handouts, or helping to answer client questions.
• Assist with data collection and analysis tasks such as entering or organizing survey responses, preparing focus group guides, or helping to summarize participant feedback.
• Identify articles for a literature review, identify key article themes, and create summaries to support project research.
• Identify key learnings and improvements from projects and contribute new and improved approaches to our knowledge management and best practice teams.

Research Associate

• This position is responsible for complex level work supporting information technology application(s) through planning, designing, implementing, maintaining, and providing ongoing optimization and support
• Fully remote but must travel as needed for mandatory meetings, site visits and go-lives
• The senior analyst is responsible for providing advanced technical support, configuration, integration, and maintenance for various healthcare applications and their technologies throughout their lifecycle
• The senior analyst may also manage small and mid-sized projects related to these applications and their technologies and will help plan and execute projects
• The senior analyst will mentor other analysts and is expected to contribute to the development of best practices and standards for application configuration, deployment, support, archival, and decommissioning.

Senior Epic Research Analyst

• Schedule and perform on-site or remote monitoring visit activities, inclusive of the following study visit types: Site Initiation Visit (SIV), Interim Monitoring Visit (IMV) / Routine Monitoring Visit (RMV), and Close Out Visit (COV).
• Contribute to the development of protocols, study tools, materials, and documentation for clinical sites.
• Provide feedback to assist sites with resolution of detected deficiencies and corrective action needed.
• Review site-level investigational drug accountability and safety event documentation.
• Review and verify patient files and records, informed consent, case report forms, and source documents for completeness, accuracy, consistency, and compliance; identify deficiencies; provide training and/or initiate corrective action as required.
• Identify, document, track, and report site protocol deviations and violations as defined within the EAP Monitoring Plan.
• Manage query resolution.
• Provide mentoring, training, and co-monitoring of junior team members.
• Assist in the development of applicable WEP Clinical Standard Operating Procedures.
• Develop applicable document templates, including (but not limited to), Monitoring Plans, Monitoring Visit Reports, Confirmation Letters, Follow-Up Letters, and Query Logs.
• Complete, review, and/or submit monitoring reports and query logs.
• Address protocol or monitoring-related questions received from clinical sites for assigned programs.

Clinical Research Associate

• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
• Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.
• Gains an in-depth understanding of the study protocol and related procedures.
• Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
• Performs remote and on-site monitoring & oversight activities using various tools to ensure Data generated at site are complete, accurate and unbiased and subjects’ right, safety and well-being are protected.
• Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.
• Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.
• Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.
• Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation Pathway as appropriate in collaboration with CRA-Manager, CRM, TA Head and CRD as needed.
• Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.
• Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.
• Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor and sharing best practices as appropriate/required.
• Supports and/or leads audit/inspection activities as needed.
• Performs co-monitoring visits where appropriate.
• Following the country strategy defined by CRD and/or CRA-Manager, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities.

Clinical Research Associate, Oncology

• This position is responsible for complex level work supporting information technology application(s) through planning, designing, implementing, maintaining, and providing ongoing optimization and support.
• Fully remote but must travel as needed for mandatory meetings, site visits and go-lives.
• Documents and recommends workflow changes and technical/functional designs needed to support the business requirements.
• Partners with external vendors to support related third-party applications including integration/implementation, support, and troubleshooting.
• Solves common and complex issues, incidents, and problems according to agreed upon service levels and according to department standards.
• Serve as PM and complete PM functions for mid-size projects with multiple teams.
• Performs quality review of team build.
• Collaboratively works with peers, internal and external stakeholders, and vendors.
• Participates in development of training and knowledge-based materials for use by peers, end-users, and other team members.

• Collaborate with team members to ensure all project deadlines are met and project logistics are accounted for
• Assist in all aspects of research across operational phases throughout the project, including survey proofing, data cleaning, data charting, data checking, recruitment updates, etc.
• Document client calls and internal meetings, including providing feedback to the relevant projects and ensuring documentation is shared with team for collaboration
• Support client deliverables by creating slides, identifying case studies, syndicated data and desk research that lend to the overall insights and narrative
• Manage logistical issues around fielding, data processing, vendors, etc., including identifying process improvements
• Proactively communicate availability/capacity/contributions to the team

Research Analyst – Custom Market Research

• Assist with survey design, questionnaires, and sampling to meet client objectives
• Act as the day-to-day contact for clients and project collaborators
• Coordinate and manage multiple projects at once, ensuring on-time and accurate delivery
• Partner with suppliers when needed to ensure high-quality data collection at reasonable costs
• Analyze and interpret final datasets, creating clear, visually engaging reports (PowerPoint or similar)
• Guide clients through findings using YouGov’s analytics tools and software

• 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 Analyst jobs in Colorado

See all jobs on JobTailor

Research Associate

Senior Epic Research Analyst

Clinical Research Associate

Clinical Research Associate, Oncology

Senior Epic Research Analyst

Research Analyst – Custom Market Research

Research Associate

Research Associate

Research Specialist