• Assist Clinical Research Associates (CRAs)/In-house Clinical Trial Manager (CTM) and Regulatory as well as Start-Up, with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines• Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. • • • • • Assist with periodic review of study files for completeness.• Assist CRAs/CTMs with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.• Assist with TMF filing, tracking of site regulatory approvals and team training reconciliation• Assist with the tracking and management of Case Report Forms (CRFs), queries & clinical data flow• Serve as a central contact for the clinical team for designated project communications, correspondence and associated documentation• Responsible for assuring projects assigned, are run according to SOPs and WP as defined organizational policy• As required, responsible to accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approvalCollection and Processing of essential regulatory documents• Communication with sites and CRAs to collect documents for submission to the IRBs• Working with sites and team members for tracking site activation• Review of ICF changes and collection of approval documents

• Development and tracking of credential data for individuals participating in a clinical trial.• Aid Investigators in the development of electronic data capturing report forms for Investigator initiated trials.• Creation of eCRFs according to protocol requirements.•Data review and cleaning for entry into the EDC system for Investigator Initiated Trials• In conjunction with management, assists with developing, documenting, and updating internal processes and processes required for consistency across programs such as SOPs, working practices, & related quality assurance forms• Maintain regular communication with study sponsors to ensure they ran smoothly, and executed any corrective action if needed.• Performing clinical data review of data listings and summary tables, answering generated queries.• Coordinated clinical trial data for a variety of the disease groups within oncology, including GYN, gastrointestinal, genitourinary, and neurologic. • Completed source document verification, query resolution on-site.• Project coordination of global trials across the US, UK, and EU• Responsible for building and maintaining positive relationships with monitors and study team• Responsible for assuring project timelines are met as per contract• Responsible for maintaining relationships for all assigned work, keeping all project reporting current, & assuring executive management is aware• Provide other project support, as assigned• Assists in the development of reporting trial data

• Determine the eligibility of subjects in order to participate in clinical trials, including Metastatic Soft Tissue Sarcoma, Urothelial Cancer, Malignant Solid Tumors, Retroviral Replicating Vectors, GIST, Glioma, IDH1 mutations & more• Communicate details of recruiting in a clear and concise manner with subjects, research staff, patient’s representatives & study personnel• Reviewing patient’s medical history and procedures in accordance to HIPAA for eligibility to study, during the screening process• Review all the elements of the screening process with the Principal Investigator to make sure Inclusion/Exclusion criteria are met• Registering/randomizing subjects according to protocol and internal policies for studies• Utilize appropriate methodologies to collect patient’s information for the research project such as labs, diagnostic tests results, schedule calendars, tracking logs, etc. entering data in various EDC systems in a timely manner• Reporting Serious Adverse Events to applicable agencies and IRB as written in the Protocol and per policy• Monitor all new amendments to the Protocol and their approval by IRB and make sure that all Subjects are re-consented if any changes were made in the Informed Consent• Active participation in weekly meetings to give feedback or receive advice about problems & information encountered in a particular study or to discuss the feasibility of a new protocol• Responsible for site initiation, interim monitoring and close-out visits for studies• Ensure the protection of subject data integrity, adherence to protocol.• Monitoring source documents, as well as verification of CRFs against patient medical records to ensure CRFs are a valid representation of the participant.• Monitoring investigational product storage, while working with pharmacy personnel to ensure accuracy & accountability

• Served as the point of contact for several international accounts.• Monitored quality assurance to prevent mistakes or defects in goods prior to delivery to the customers.• Liaised with several departments in order to successfully achieve client requests and execute sales operations in a timely manner.• Daily analysis of internal & external reports to manage and record data, to refine and improve customer service.• Estimated cost analysis for client to reach optimal supply and demand.• Aided in the research and reformatting of fiscal budget.

• Assisted in the redesign of the Tom Ford International website, executed with their Creative Imaging Department in the repopulation of multiple seasons of Menswear collections. Implemented particular marketing strategies in line with the image of, in attempt to elevate the brand • Participated in outreach to sustain excellent customer service, while being proactive in creative industries and community relations at large. Oversaw international location shoots, which involved the handling of a carnet that lead to an expedited customs process• Coordinated pre-and-post photo shoot logistics as a Wardrobe Stylist and assistant, to ensure all wardrobe, accessories, props and accoutrements were collected & returned in pristine condition • Handled all inquiries related to potential conflicts of interest among multiple companies, while monitoring and managing plans in regards to the production process, while also adhering to all necessary policies • Led, as well as assisted in the on-set/location styling of outfits for Victoria’s Secret, Bloomingdales, Sundance Catalog, By Robert James, Alue Optics, Vente-Privee, Chico’s, Redcats, Avon & Hearts on Fire Jewelry for editorial, catalogue, e-commerce and photo-shoots for womenswear and menswear

• Oversaw the research and editing of State Parks programs for Data entry into a digital platform for a mobile application• Responsible for data auditing to improve accuracy prior to entry on the social media platform• Wrote content and created a weekly playlist for the Parks By Nature blog, in relation to different themes in nature to better market and promote the brand

• Aided editors, fashion stylists, and costume designers to style celebrities, models, and actors for advertising campaigns, awards shows, and television appearances• Facilitated the transition to a new merchandise tracking and cataloguing system within a 7,500 sq. ft showroom which has resulted in faster product retrieval and inventory management

• Led the permit request process for over 1,200 projects filmed and photographed in the City of Miami• Facilitated the pre-production permit process which included coordinating with property owners, Police and Parks departments and insurance companies• Managed scouting locations for the production of the following television shows, movies, and commercials: Burn Notice, Marley & Me, New In Town, Away We Go, Dinner and A Movie, MTV Promos• Worked in concert with three different Film Offices (City of Miami Beach, Miami-Dade County, and Broward Film Alliance) to ensure permits were in place for multi-jurisdiction film productions• Standardized the permit tracking process which helped improve the budgeting and planning process for City Manager of Miami • Identified and developed a residential film ordinance which defined the guidelines for filming on private property, such as crew size, length of shoot, and permit requirements

• Managed logistics during Art Basel, for the leading US contemporary satellite art fair, attended by 28,000+ patrons: managed list compilation, ticket management, and delivery routes for production staff • Supervised delivery and placement process of art for over 120 galleries, including 1,100+ sculptures, paintings, and mixed media and digital installations• Aided in execution and delivery of signage and sponsorship collateral for twenty-four corporate sponsors: industries included hospitality, travel, beverage, insurance, and media• Identified and managed in the assistance of over 500 VIPs, which included musical talent, art buyers, and celebrities

• Performed data entry, list compilation, and image requests for the publication of three issues of the magazine• Acted as a liaison between sales and advertisers to help coordinate the delivery of advertising and payments