Role Description As a Principal Researcher / Research Manager, you operate in three modes: - Stand up the research operating model for Multiplier: - Co-create how research runs as a function with the Snr Director. - Set the strategy and standards the discipline operates by. - Set and execute research strategy at the pillar level: - Own the research agenda for one pillar. - Lead the highest-stakes studies. - Partner directly with product, design, and engineering leaders. - Support research across EPD through your team: - Build and grow a team of researchers embedded across other pillars. - Act as their coach, soundboard, and collaborator. Qualifications - 8–12+ years of UX research experience, including leading research in complex product environments. - Proven ability to define multi-quarter research strategy and influence senior product decisions. - Deep craft across generative, evaluative, and mixed-methods research. - Experienced in managing and growing a team of researchers. - Strong systems thinker who connects insights across surfaces and squads. - Confident influencing senior product, design, and engineering leaders. - Motivated to build durable research capability inside a scaling organization. - Experience designing how a research function runs at scale. Requirements - Define how research operates end-to-end across EPD. - Set tooling and procurement strategy. - Establish research compliance standards. - Define a research strategy aligned to the pillar's 1–2 year product ambition. - Lead the hardest studies personally. - Coach researchers on problem framing, method choice, and synthesis. - Own hiring, performance, and staffing for researchers across EPD. - Define what "good research" means at Multiplier. Benefits - Flexible / Global work location. - Opportunity to influence roadmap and strategy decisions. - Work in a collaborative environment with a focus on growth. Company Description Multiplier is building the world's leading Global Human Platform, enabling companies to hire, onboard, manage, and pay talent across 150+ countries. Our platform simplifies complex international employment infrastructure so businesses can scale without borders.

Title: Research Associate - Psychiatry - PT Location: Jackson United States time type Part time job requisition id R00050922 Job Description: Hello, Thank you for your interest in career opportunities with the University of Mississippi Medical Center. Please review the following instructions prior to submitting your job application: - Provide all of your employment history, education, and licenses/certifications/registrations. You will be unable to modify your application after you have submitted it. - You must meet all of the job requirements at the time of submitting the application. - You can only apply one time to a job requisition. - Once you start the application process you cannot save your work. Please ensure you have all required attachment(s) available to complete your application before you begin the process. - Applications must be submitted prior to the close of the recruitment. Once recruitment has closed, applications will no longer be accepted. After you apply, we will review your qualifications and contact you if your application is among the most highly qualified. Due to the large volume of applications, we are unable to individually respond to all applicants. You may check the status of your application via your Candidate Profile. Thank you, Human Resources Important Applications Instructions: Please complete this application in entirety by providing all of your work experience, education and certifications/ license. You will be unable to edit/add/change your application once it is submitted. Job Requisition ID: R00050922 Job Category: Research Organization: SOM-Psychiatry-Neurobiology and Behavior Research-PI Location/s: Main Campus Jackson Job Title: Research Associate - Psychiatry - PT Job Summary: The Research Associate is a key member of a research team, responsible for conducting experiments, analyzing data, and contributing to scientific investigations. This position is ideal for candidates with a strong scientific background who are eager to engage in independent and collaborative research projects. Education & Experience Education and Experience: Master's Degree in a field of science or Bachelor's in a field of science and two (2) years of laboratory experience Certifications, Licenses, or Registration Required: N/A Preferred Qualifications: Research experience in academic or industry setting Knowledge, Skills & Abilities Responsibilities: - Design and execute experiments under the direction of the principal investigator (PI). - Conduct molecular, cellular, and/or biochemical assays as part of research studies. - Collect, analyze, and interpret experimental data using statistical and imaging software. - Contribute to manuscript preparation and presentation of research findings. - Maintain accurate and detailed laboratory records. - Collaborate with research teams to support multiple ongoing studies. - Train and mentor junior staff, students, or research assistants providing guidance on laboratory procedures and best practices. - Manage laboratory inventory, ensuring proper ordering and organization of supplies and reagents. - Maintain and troubleshoot laboratory equipment, coordinating maintenance and repairs as needed. - May assist in animal husbandry, collection of physiological data, and euthanasia. - The duties listed are general in nature and are examples of the duties and responsibilities performed and are not meant to be construed as exclusive or all-inclusive. Management retains the right to add or change duties at any time. Physical and Environmental Demands: Requires frequent bending at the waist, frequent crouching/stooping, occasional kneeling, frequent reaching, occasional carrying/lifting up to 75 pounds, occasional push/pulling, frequent walking, frequent standing, frequent sitting, occasional driving, occasional frequent exposure to unpleasant or disagreeable physical environments such as high noise level and exposure to heat and cold, occasional handling or working with potentially dangerous equipment/machinery, occasional exposure to bio-hazardous conditions such as risk of radiation exposure, bloodborne pathogens, fumes or airborne particles, and/or toxic or caustic chemicals, which mandate attention to safety considerations, occasional working hours significantly beyond regularly scheduled hours, occasional travelling to offsite locations, occasional activities subject to significant volume changes of a seasonal/clinical nature, and constant work produced subject to precise measures of quantity and quality. Time Type: Part time FLSA Designation/Job Exempt: Yes Pay Class: Salary FTE %: 50 Work Shift: Day Benefits Eligibility: Grant Funded: Yes

• You will be dedicated to a single client • You will be responsible for all site management and supervisory activities in the assigned oncology studies. • You will work with industry leaders and subject matter experts. • You will have the opportunity to mentor junior CRAs. • You will work with world-class technology. • You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.

• Perform site management activities to ensure compliance with the protocol, monitoring plan, ICH GCP, local regulatory requirements, and client SOPs. • Conduct site qualification, initiation, interim, and close-out visits, both on-site and remotely. • Partner with Clinical Trial Liaison (CTL) and other client functions to support site activation and deliverables. • Establish and maintain productive professional relationships with investigator site staff, ensuring effective communication and problem-solving throughout study conduct. • Perform drug accountability, reconciliation, and destruction, ensuring protocol compliance for storage and shipment requirements. • Prepare and maintain Oversight Monitoring Plan. • Conduct Oversight Monitoring Visits at sites, either independently or alongside CRO CRA. • Ensure site regulatory files are current and verify timely submission of study documentation, including safety reporting. • Identify and record protocol deviations, escalate non-compliance, and resolve study-related issues as necessary. • Maintain ongoing communication with site personnel, study teams, CTLs, Central Monitors, and CRO CRAs.