Research Analyst

• Serves as an initial point of contact for individuals and groups providing basic information about result analysis and methodologies, answers questions as needed
• Maintains organization of research records and responds to data requests and inquiries
• Prepares reports and manuscripts and assists with the development and presentation of materials through various communication platforms
• Analyzes data and summarizes research results for a defined research area or study by utilizing established processes

IRP Research Analyst

• Support the research team in the conduct of department research projects
• Perform study startup, implementation, and closeout activities
• Assist research team with coordination and entry of research data
• Assist with regulatory submissions to the Institutional Review Board, and maintain compliance with all federal and local agencies in accordance with Good Clinical Practice guidelines
• Interact with patients and families for securing informed consent, scheduling research visits, and collection of data
• Maintain documentation for regulatory binder, adverse event reporting, and communications between sponsors and sites
• Other special skills specific to assigned research area may include phlebotomy, sample collection, processing or shipping, ECGs, chart abstraction or other duties as assigned
• Manage personal career development and administrative tasks

Clinical Research Associate – Cancer and Blood Disorders

• Develop clinical trial budgets, including review of protocols and relevant documents to ensure that appropriate costs and allocation of institutional resources are fully captured in the budget.
• Work in collaboration with ancillary teams, departments, investigators, research staff, supporting administration, and sponsors/funding agencies to create complete, comprehensive, accurate and timely budgets.
• Ensure appropriate research rates are applied to study budgets.
• Independently develop, negotiate, and finalize budgets of moderate complexity with sponsors, academic sites, and other extramural funding sources to reach an agreement on budget and payment terms.
• Submit and maintain the budget and other financial information into OnCore Clinical Trial Management System (CTMS) to maintain proper reimbursement and revenue integrity.
• Perform pre-award quality assurance to verify completion of required elements prior to Medicare Coverage Analysis.
• Communicate and meet with stakeholders to facilitate ongoing budget discussions and provide updates to relevant parties.
• Use advancing knowledge to develop and disseminate clinical research education as needed in accordance with federal regulations, institutional policies, and specific protocol requirements.
• Apply knowledge of clinical research to provide recommendations and direction to clinical research teams to ensure budgetary compliance throughout all phases of the Clinical Trial Financials Lifecycle.
• Develop and support the formulation of program policies, procedures, and resources to establish and enhance clinical trial financials workflows.
• Provide excellent customer service while maintaining accurate results in a fast-paced, deadline-driven team environment.
• Engage in special projects and ad hoc duties as a member of the administrative team.

Clinical Trials Budget Specialist II

• Translates business requirements into business solutions;
• Acts as liaison between departmental leaders, staff and information technology staff to design and configure business solutions to ensure business requirements have been met.
• Works closely with stakeholders to define business requirements and with technical staff to develop solution alternatives and actively participates in defining objectives to support changing business needs and availability.
• Coordinates IT troubleshooting and day to day activities within the department to ensure seamless and minimal downtime of hardware, software and reporting requirements.
• May manage small to mid-sized projects/tasks and represent the department on larger enterprise-wide project teams.
• Creates and maintains project schedules by developing project plans and specifications, estimating time requirements, establishing deadlines, monitoring milestone completion, tracking all phases of the project product/service lifecycle, providing timely reporting of issues that impact project progress, coordinating actions, and resolving conflicts.
• Coordinates and conducts project team meetings regularly to review project deliverables and deadlines.
• Has knowledge and experience in the various techniques to elicit, analyze and communicate requirements within assigned functional areas.
• Establishes test plans, test cases and executes testing.
• Assists with end user training.
• Recommends information technology solutions to meet business needs and coordinates the planning, development, and implementation of these solutions.

Business Analyst II

• Provide leadership and oversight for extensive research operations
• Direct supervision of 2.0 FTE and indirect supervision of 7.0 FTE
• Compile, analyze, and present data on proposal statistics, award information, trends, and national rankings
• Ensure timely and accurate financial reports are provided and discussed with principal investigators
• Lead and coordinate DOP Research & Development grant proposals/awards and Capital Equipment allocations
• Develop/lead research administration education opportunities and trainings for faculty, staff, and trainees

Research Program Associate Director

• Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance.
• Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials.
• Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience.
• Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards.
• Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy.
• Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey.
• Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance.
• Possesses experienced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development.
• Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues.
• Identifies, evaluates and recommends new/potential investigators/sites on an on going basis.

Clinical Research Associate II – Oncology

• Documents and maintains Standard Operation Procedures
• Participates in novel pathogen testing
• Performs literature reviews
• Collects data and monitors test results

Research Specialist

• Reviews and perfects tax returns while staying on top of the latest tax code changes
• Leads exciting client projects, with a focus on Partnership tax
• Dives into tax issues, prepares insightful memos, and optimizes client tax strategies
• Guides and mentors staff, develops quality control procedures, and drives business growth
• Supports tax compliance, conducts in-depth research on tax laws and regulations, and provides actionable insights
• Oversees the preparation and review of complex returns, ensuring compliance with tax law
• Develops strategies to optimize tax liabilities
• Manages client relationships, mentoring staff, and keeping the team updated on changes in tax regulations

Tax and Research Specialist

• preparing images for evaluation
• classifying observed changes
• entering data into FDA compliant electronic case report forms
• participating in quality control exercises
• performing literature reviews and writing reports
• reviewing, analyzing, and interpreting data and/or documents results for presentations and/or reporting to internal and external audiences
• providing operational guidance on day-to-day activities of unit or program staff and/or student workers
• operating, cleaning, and maintaining organization of research equipment and research area
• tracking inventory levels and placing replenishment orders
• participating in the development, interpretation, and implementation of research methodology and materials
• conducting research experiments according to established research protocols

Research Specialist – Grader

• Support the research and work by managing data, recruiting and scheduling participants, analyzing data, and contributing to community outreach and education.
• Work independently and as part of a group on both projects simultaneously.
• Perform literature reviews and write reports.
• Review, analyze, and interpret data and/or documents results for presentations and/or reporting.
• Conduct research experiments according to established research protocols.
• Collect data and monitor test results.
• Participate in the development, interpretation, and implementation of research methodology and materials.
• Operate, clean, and maintain organization of research equipment and research area.
• Track inventory levels and place replenishment orders.
• Provide operational guidance on day-to-day activities of unit or program staff and/or student workers.
• Engage with community groups to support research outreach, recruitment, and strengthen community partnerships.

• 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

• Investigate and interpret data, turning research into clear, concise executive memos, diagrams, and presentations.
• Support research for projects regarding business competitors and non-profit organizations.
• Collaborate with business units to understand their challenges and recommend solutions to senior management.
• Edit and proofread memos, emails, presentations and reports.

• Perform study startup, implementation, and closeout activities
• Assist research team with coordination and entry of research data
• Assist with regulatory submissions to the Institutional Review Board, and maintain compliance with all federal and local agencies in accordance with Good Clinical Practice guidelines
• Interact with patients and families for securing informed consent, scheduling research visits, and collection of data
• Maintain documentation for regulatory binder, adverse event reporting, and communications between sponsors and sites
• Other special skills specific to assigned research area may include phlebotomy, sample collection, processing or shipping, ECGs, chart abstraction or other duties as assigned
• Manage personal career development and administrative tasks

Research Analyst jobs in Wisconsin

See all jobs on JobTailor

IRP Research Analyst

Clinical Research Associate – Cancer and Blood Disorders

Clinical Trials Budget Specialist II

Business Analyst II

Research Program Associate Director

Clinical Research Associate II – Oncology

Research Specialist

Tax and Research Specialist

Research Specialist – Grader

Research Specialist

Research Specialist

Research Analyst

Clinical Research Associate I