Alyse Hall, Bs, Pmp Email & Phone Number

Frisco, Texas, United States

New York, New York, Us

• METHODICAL & ORGANIZED - Organized & cleanly tracks project deliverables through proficient interpersonal skills to drive conversations & decisions; meets with project teams through advanced scheduling & coordinating techniques to meet stakeholder deadlines & address any blockers; prepares data analysis to relay project statuses to management & stakeholders; has extensive understanding of critical project management techniques.• TEAM LEADER - Accountable & growing leader who mentors others by being a role model & support for individual development; provides detailed performance review input & development recommendations for key contributors; consistently improves project management skills through extracurricular means, such as being accepted & completing the 2022 - 2023 Prometheus Program - Dallas Chapter. Prometheus is a 9-month, female talent development initiative for AVP & Officer female talents that focusses on coaching women for career advancement. Elected team leader for local team challenge.• STRONG COMMUNICATOR - Sponsor/ Project Owner/ Business Leads/ Regulatory & Compliance communication, creating standards/ policies. Coordinates interface between project owners & Subject Matter Experts to drive projects to timely completion.• ATTENTIVE TO DETAIL - Develops procedures to determine End User eligibility for platform/ technology migrations; closely tracks successes/ failures/ complications with migration activities to address/ remediate issues quickly to prevent future reoccurrences.• MEETS DEADLINES - Completes project deliverables on-time.• Awarded for driving migrations for 230k+ user Outlook mailboxes to new cloud-based messaging platform, Office 365 email/ Exchange Online. • REGULATORY COMPLIANCE - Ensures regulatory compliance of all projects (as applicable) & other project programs. Management of regulatory site files, prepare for internal & external audits. Project Management | IT | Team Leader | CRO | Operations | Reading Enthusiast

New York, New York, Us

• METHODICAL & ORGANIZED - Cleanly tracks project deliverables for timely completion through skilled interpersonal skills to help drive conversations/ decisions; consistently meets with project teams to work towards deadlines & address/ review any blockers; prepares data analysis to clearly relay project metrics/ statuses to upper management & stakeholders.• TEAM LEADER - Consistently improving project management skills through extracurricular means, such as being accepted & completing the 2022 - 2023 Prometheus Program - Dallas Chapter. Prometheus is a 9-month, female talent development initiative for AVP & Officer female talents that focusses on identifying, developing, & sponsoring women for career advancement & potential future leadership opportunities. Elected Team Leader for Local Challenge Project which created automated reporting for tracking Exchange Online migrations globally.• STRONG COMMUNICATOR - Sponsor/ Project Owner/ Business Leads/ Regulatory & Compliance communication, creating standards/ policies. Coordinates interface between project owners & Subject Matter Experts to drive projects to timely completion.• ATTENTIVE TO DETAIL - Develops procedures to determine End User eligibility for platform/ technology migrations; closely tracks successes/ failures/ complications with migration activities to address/ remediate issues quickly to prevent future reoccurrences.• MEETS DEADLINES - Completes project deliverables on-time.• AWARDED for driving execution of overall meeting room space strategies, allowing team to achieve high amounts of Zoom Room deployments along with a go-forward approach to integrating both Exchange Online & Zoom. • REGULATORY COMPLIANCE - Ensures regulatory compliance of all projects (as applicable) & other project programs. Management of regulatory site files, prepare for internal & external audits. Project Management | IT | Team Leader | CRO | Operations | Reading Enthusiast

Dallas, Texas, Us

• STRONG COMMUNICATOR - Sponsor/ Principal Investigator communication, writing study consents/ HIPAA forms/ research protocols. Coordinates interface between clinical trials & basic/ clinical research collaborators at university & other institutions.• ATTENTIVE TO DETAIL - Develops procedures to determine subject eligibility; screens; recruits; & enrolls subjects, ensuring & documenting proper informed consent; tracks subjects’ information from multiple projects. • METHODICAL & ORGANIZED - Screen & recruit research subjects, data collection & entry, obtain informed consent from research subjects, create case report forms (CRFs). Develops & maintains data collection & management of clinical research program registry information.• MEETS DEADLINES - Prepare IRB submissions, Prepare study budgets.• AWARDED the Highest Accruing Site for 2018 & 2019 on the clinical trial I co-led (the ECOG-ACRIN (EA) TMIST clinical trial) at UT Southwestern & was invited to attend the EA Fall Conference to present on how UT Southwestern maintained high recruitment & data management.• QUALITY ASSURANCE - Assist with coordinating, developing, & implementing research studies to include writing clinical trials, & review research study procedures to ensure receipt, completeness, & accuracy of research data required while ensuring regulatory compliance.• PATIENT ORIENTED - Assists in design of research survey forms to capture required patient information; directly interacts & interviews research study subjects &/or family members to gather required study information.• TEAM LEADER - Provides general scientific support for clinical research program staff & university business office.• REGULATORY COMPLIANCE - Ensures regulatory compliance of the TMIST clinical trial & other clinical research programs. Management of regulatory site files, prepare for internal & external audits. Project Management | IT | Team Leader | CRO | Operations | Reading Enthusiast

Dallas, Texas, Us

Geneva, Switzerland, Ch

• ATTENTIVE TO DETAIL - Participated in multi-dose preservative free eye drops testing to successfully establish proof of concept (over 127,500 doses in total).• HIGHLY ADAPTABLE - Interpreted Regulated Stability Protocols to create LIMS protocols.• ORGANIZED - Planned & implemented reorganization of Stability Chamber areas to improve functionality & space utilization. • LEADER - Led project for decommissioning over 220 laboratory instruments & computers.• QUALITY - Supported Novartis/Alcon Medical Device Analytics with transferring over 25 scientific instruments, documentation/data entry, change control deliverables, document review, & physical moves. • TEAM PLAYER - Demonstrated cross-functional collaboration with management, Facility Operations group, Metrology, QA, IT, Ocular Bioinformatics, vendors, & service providers.• INNOVATIVE - Created new forms & SOPs in electronic database (Documentum) for site-wide use.Project Management | IT | Team Leader | CRO | Operations | Reading Enthusiast

Dallas, Texas, Us

• CREATIVE & ATTENTIVE - Streamlined process for Radiology faculty requesting office/ laboratory space by authoring a Standard Operating Procedure (SOP), while addressing new information as needs evolved.• MULTITASKER - Assisted both Chairman & Vice Chairman of the Dept. of Radiology; duties included meeting minutes, expense reports, maintenance of travel, handling proprietary documentation/ information, & handling personal calendar organization.Project Management | IT | Team Leader | CRO | Operations | Reading Enthusiast

Wilmington, Massachusetts, Us

• LEADER - Lead formulator of various dosing methods resulting in launch to clinical trials in several countries; clean technique & Good Laboratory Practices (in accordance to SOPs & FDA regulations) were utilized to accurately document observations & maintain integrity of produced formulations.• CAPABLE - Selected by management to prepare experimental dosing material needed for FDA fast-tracked drug approval in 2014; data was captured on new electronic preparation system during program start-up.• TRAINER - Chosen by management to be Principal Trainer for new & existing employees on safety/Personal Protective Equipment (PPE) requirements, data management, performing various lab techniques in the presence of clients & auditors, interpreting client protocols, scheduling departmental duties based on client needs, customer service, etc. while continuing to foster a team environment & maintaining continued competency in the lab.• PROJECT COORDINATOR - Managed over 72 GLP & non-GLP toxicology projects run at CRL-Reno in 2013-2014 through methodical preplanning, timely execution, collaborating with management & other departments, teamwork, data review, & constant vigilance over project updates.• ORGANIZED - Ordered & managed laboratory supplies, maintained equipment maintenance/calibration records, wrote & revised SOPs, maintained new hire laboratory training, led & assisted with laboratory studies.• QUALITY - Experienced with addressing & identifying deviations (protocol, GLP, SOP, Maintenance) & addressing quality assurance audits (internal & external) swiftly to further strengthen the integrity of collected data & provide excellent customer service to clients.Clinical Research Coordinator | Team Leader | CRO | Lab Technician | Operations | 5K Enthusiast

Wilmington, Massachusetts, Us

• ATTENTIVE TO DETAIL - Interpreted Regulated Protocols to create template forms/ labels used for sample processing.• QUALITY - Ensured compliance with GLP Standards, wrote study protocols, protocol deviations, final study reports, & served as Quality Assurance Unit.• LEADER - Chosen by management to represent department in Black Belt initiative to address CAPAs & improve interdepartmental communication to rid roadblocks/delays in workflow.• ATTENTIVE TO DETAIL - Performed sample processing, storage, & shipment/transfer as exactly specified by the client, as well as chemical titrations & custom-designed studies.Project Management | IT | Team Leader | CRO | Operations | Reading Enthusiast