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.

• Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies • Serve as the main CTI contact for assigned study sites • Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in the Monitoring Plan while adhering to all applicable regulatory requirements, SOPs, and ICH GCP • Assist with study start-up activities, including feasibility, pre-study activities, and site selection • Collect, review, and track essential/regulatory documents • Participate in and complete all general and study-specific training as required • Participate in investigator, client, and project team meetings • Create and implement subject enrollment strategies for assigned study sites • Ensure proper storage, dispensation, and accountability of all Investigational Product (IP) and trial-related materials • Perform site management activities and provide ongoing updates of site status to the Clinical Project Manager • Conduct remote monitoring and complete related activities in accordance with study-specific Monitoring Plan • Utilize systems and reports to track subject status, subject case report form (CRF) retrieval/source document review (SDV), regulatory documents, and IP • Assist with project-specific activities as a member of the Project Team • May support in the development of CRFs and other study-related documents (subject worksheets, Monitoring Plan, etc.) • May support in the translation, customization, and review of Patient Information sheet and Informed Consent, protocol synopsis, and other study-applicable documents as per required procedures • Where applicable, provide support to the Regulatory Affairs Study Start-up Team in the preparation or revision of documentation for submission to Ethics Committee(s), Institutions' Ethics Committees, Regulatory Authorities, Competent Authorities or Institutions Administration Boards, and follow up on the evaluation process until approval is available. • Provide regular updates to the Sponsor/ Client • Assist in preparing and coordinating Investigator and client meetings, and attend meetings as necessary • Liaise with Clinical Data Management for data cleaning activities • Identify site issues and implement corrective actions or escalate as appropriate • Manage ISF and TMF for all assigned study sites in accordance with SOPs or study-specific Monitoring Plans • Where applicable, support in contract negotiation with study sites, Investigator payments, and tracking of site payments