TAKIYAH GIBSON, CSM, SSM

Durham, NC ***** 803-***-**** adx8hv@r.postjobfree.com Linkedin SCRUM MASTER

Agile Champion passionate about fostering Agile Scrum methodologies, business assessment, and management of all facets of software and system development life cycle from preliminary design to development, implementation, and delivery. Adept at instructing and ascertaining constant application of major Agile principles and scrum processes, including collaboration, prioritization, team accountability, and visibility. Efficient in adoption and execution of scrum rules, mitigating discrepancies, and spearheading high-performing teams. Proficient in monitoring sprint metrics, fostering automated status reports by utilizing dashboards in JIRA, mediating complications, and leading numerous scrum processes to achieve project objectives.

CORE COMPETENCIES

● Scaled Agile Framework

● Strategic Planning & Execution

● Project Metrics & Dashboards Creation

● Retrospectives & Reviews

● Risk Mitigation

● Project Management

● PI Planning

● Quality Control Initiatives

● Data Analysis

● Business Prioritization

● Problem Resolution

● Jira & Confluence

PROFESSIONAL EXPERIENCE

Premiere Web Solutions (Remote) January 2023 – Present SCRUM MASTER

Instill Agile principlicples and values while supporting Agile team by removing impediments, facilitating Scrum Ceremonies (Daily Scrum, Sprint Retrospective, Sprint Planning, Speint Demo. Determine team capacity of all team members for program optimization. Prepare presentation materials regarding sprint data for leadership. Attain desired results by meeting deadlines, informing key parties, formulating mitigation strategies, andexecuting plans. Enable team to accomplish projects within timelines by boosting efficiency across teams through advancedtechnologies. Defined all work iterations, risks, dependencies, and program goals by contributing to pre-planning and PI Planning efforts.

• Developed team working agreements, PTO tracker, and meeting recordings by making custom team pages in Confluence to maintain transparency and visibility across teams.

• Conduct sprint retrospectives using various sprint retrospective tools, such as Easy Retro, IdeaBoardz, Mural, and Miro and developed a safe environment, allowing developers to freely converse during retrospectives.

• Offer guidance and support to maximize agility within teams by collaborating with agile team

• Instructed team to design project-specific user stories, including value statements, acceptance criteria, assumptions, and associated tasks.

• Assist product owner and team members in grooming backlog and warranting continuous flow of operations.

• Resolve various issues and directed activities for project goals by overseeing sprint metrics and scheming automated status reports using dashboards, including sprint burn-down widgets, risks, and team and user story statistics in Jira.

• Integrated and governed user stories, epics, and child tasks for multiple products by utilizing Jira.

• Cultivate high-level dashboard to monitor/assess sprint metrics in Jira by leveraging burn-down chart and other sprint filter gadgets.

• Analyze sprint capacity by utilizing historical sprint data assessment and sprint capacity evaluation. IQVIA, Durham, NC November 2022 – Present

REGULATORY START-UP SPECIALIST I

• Performed tasks at a country level associated with Site Activation (SA) activities by applicable local and/or international regulations, SOPs, project requirements, and contractual/budgetary guidelines.

• Served as a Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.

• Complied and maintained adherence to SOPs, Work Instructions (Wis), quality of designed deliverables, and project timelines.

• Executed start-up and site activation activities according to applicable regulations, SOPs, and work instructions. Distribute completed documents to sites and internal project team members.

• Accurately completed and maintained all internal systems, databases, and tracking tools with project-specific information.

• Reviewed, tracked, and followed up on the progress, approval, and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release papers in line with project timelines.

• Provided local expertise to Site Activation Managers (SAMs) and project team during initial and ongoing project timeline planning. UNC Lineberger Comprehensive Cancer Center, Chapel Hill, NC June 2021 – March 2022 REGULATORY ASSISTANT

• Gathered, edited, analyzed, and reported data/information to communicate with the IRB and research Sponsors.

• Orchestrated the actualization of new data production/generation, editing, and formatting reports to ensure accuracy.

• Proactively trained and collected training on IBs and Protocols from active research staff for GI Pod.

• Collected 1572 IB AoR and PSP from PI and Gathered FDFs, CVs, MLs, and GCP from PI and Co-Investigators.

• Complete Study Specific DoA Logs and keep them up to date in the eReg binder and CTSU

• Process Protocol amendments, initial approvals, renewals, modifications, and expedited reports sent from the Regulatory Palmetto Retina Center, West Columbia, SC September 2020 – June 2021 CLINICAL RESEARCH REGULATORY COORDINATOR/QUALITY SPECIALIST

• Regulatory maintenance requirements and following SOPs

• Submit study start-up regulatory documents to Sponsors such as FDA 1572, Financial Disclosure Forms, CVs, Medical Licenses, Protocol Signature Page, Investigator Brochure Signature Page, etc.

• Quality check all updated Informed Consent Forms for accuracy and completeness

• Submitted Investigator Applications for study site and completed Continuing Reviews for all current studies to the IRB

• Keep all Investigator Site Files (ISFs) up to date and current with the necessary essential documents for each study

• Quality check all Investigator Site Files (ISFs) for completeness, write-overs, and errors before monitoring visits Nephron Pharmaceuticals Corporation, West Columbia, SC December 2018 – March 2020 QUALITY SPECIALIST

• Assured compliance with FDA regulations in good manufacturing practice (GMP), non-conformance investigations, planned deviations, or corrective and preventive actions (CAPAs).

• Supervised the CAPAs, planned deviations, and/or non-conformance report programs (NCR); coordinated investigations and timely completion of CAPAs, planned deviations, or NCRs.

• Thoroughly performed product research and analysis to identify updated operations efficiency and productivity trends.

• Directed, updated, and constantly maintained Drug Product Quality complaints to physical or electronic logs. General Information Services, Chapin, SC September 2015 – December 2017 PUBLIC CRIMINAL RECORDS DATA ENTRY ASSOCIATE

• Reviewed criminal backgrounds of applicants for employers throughout the United States and reported findings to clients.

• Carefully compiled and documented confidential and sensitive information into the database quickly and accurately.

• Proactively communicated and coordinated with clients to resolve issues and concerns related to criminal records. ADDITIONAL EXPERIENCE

Yale Comprehensive Cancer Institute, New Haven, CT REGULATORY ASSISTANT (Activation) March 2022 – November 2022 Nephron Pharmaceuticals Corporation, West Columbia, SC QUALITY INSPECTOR July 2018 – December 2018 Carolina Medical Research, Clinton, SC CLINICAL RESEARCH COORDINATOR INTERN July 2019 – August 2019 South Carolina Department of Mental Health; Bryan Psychiatric Hospital, Columbia, SC ACTIVITY THERAPIST. Dec 2017 – April 2018 South Carolina Department of Education, Office of Health and Nutrition, Columbia, SC PUBLIC HEALTH INTERN Jan 2017 – May 2017 EDUCATION & PROFESSIONAL DEVELOPMENT

Bachelor of Science - BS, Public Health Completed: 2017 Benedict College Colombia, SC Activities and societies: National Honor Society of Leadership and Success CERTIFICATIONS

CSM - Certified Scrum Master, Scrum Alliance - 2023 SSM - SAFe Scrum Master, Scaled Agile - 2023

TECHNICAL SKILLS

Microsoft Office Suite (Word, Excel, PowerPoint, Outlook), Google Suite, Jira, Confluence, Miro, Mural, Rally, Azure DevOps

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