Robin Root Email & Phone Number

Fort Lauderdale, Fl, Us

Pensacola, Fl, Us

Pensacola, Fl, Us

VP of Operations with oversight of all aspects of research and clinical trial projects and products. My division provides project management services to both ASP and Technology Transition partners, customer and product support and data delivery for all ActiGraph medical devices.

Tempe, Arizona, Us

VP of Operations with oversight of quality and timely delivery of EDC solutions to biopharma clients. My division provides project management services to both ASP and Technology Transition customers; study design and development services on OmniComm’s TrialMaster EDC platform; EDC deployment services; and customer support.

Ft. Lauderdale, Fl, Us

Manages and reports on multiple projects; develops and maintains full project timelines for new study build, deployment, maintenance, close and archive of studies in EDC for OmniComm clients. Also manages non-EDC projects as needed such as migrations, integrations, etc. Assembles and drives cross-functional project teams, identifies resources needed, and develops detailed project plans and schedules to ensure on-time completion of clinical projects. Communicates frequently with team members and senior business stakeholders regarding project status, and identifies and resolves project problems, issues and risks. Initiates action to identify and resolve project problems/issues and reports on mitigating steps and actions taken to ensure timely deliverables, project success and quality. Takes a leadership role in training and mentoring other Project Managers and developing methods for continuously improving productivity and efficiency within the organization. Works collaboratively with Business Development on client relationship building, promoting customer satisfaction, and strategies to promote repeat business. Works collaboratively with other Project Managers to develop and implement project planning methodology, tools and standards, to promote consistency in project execution at OmniComm Systems. Cultivates inter-departmental relationships. Promotes a positive and fun work environment.

Wilmington, Nc, Us

Manages day-to-day operations for a group of clinical data management projects or key functions as well as the project staff and workloads for direct reports. Responsible for customer contact, functional, administrative and financial oversight of projects assigned and provides supervisory functions for individual contributing staff within the clinical data management department including training and mentoring of staff. Participates in business development activities as required and may perform the Project Management role for studies that do not have a clinical component or act as Franchise Manager for allocated clients. Assists senior management with the formation and implementation of strategic development plans for the department and participates in the development and implementation of processes, procedures and training for the data management function.

Raleigh, North Carolina, Us

Global leader of Clinical Data Technology services including, but not limited to, database programming, electronic data capture (EDC) and IVRS/IWRS activities with operational and financial responsibility for the execution of services against the strategic Global Clinical Data Technology plan. Worked together with all Directors within the organization to ensure overall consistency and success. Direct responsibility of successful delivery of clinical data technologies for projects led within the area and for financial performance and personnel, sales, marketing strategy, business partnerships and overall quality deliverables for CDT. Worked in partnership with Biostatistics, Clinical Data Management and Information Technology Leadership to ensure global standardization of services and maintenance of global standards, policies and procedures. Worked closely with Clinical Operations to ensure cohesive project delivery through cooperation and collaboration.

Raleigh, North Carolina, Us

Ensured that the Biometrics Brand had a well defined and consistent approach to the collection and reporting of metrics. Monitored global financial and sales performance across regions and assisted the VP of Global Biometrics in determination and tracking of key metrics. Ensured that a global project list was maintained including current and future resourcing requirements and maintained systems for tracking value of new awards and forecast opportunities for Biometrics. Maintained and supported pricing algorithms, proposal text and the overall bidding process within Biometrics, and assisted in the selling process, as needed.

Raleigh, North Carolina, Us

Developed a process for tracking the amount, timing, and scope of EDC training for each Kendle project. Worked with Kendle IT and EDC support services to develop specifications for a system to support the training tracking and manage the development of the system. Conducted EDC training as needed, assigned trainers to projects and assured all documentation of EDC training was collected and available. Worked with functional representatives to develop training assessments and with work eKendle College (online training system) to develop EDC training courses and supported business development efforts for EDC studies, as needed.

Raleigh, North Carolina, Us

Primary Kendle clinical data management (CDM) contact with Sponsors and represented CDM on Kendle project teams. Responsible for project timelines, deliverables, financial results, reporting and overall quality, as well as the data clean-up process through data archival. Approved the building, testing and validation of clinical databases and coordinated the receipt and processing of information for projects as well as electronic data received from specialty groups utilized on projects. Responsible for the creation and maintenance of CDM project budgets and Project Plan (operating procedures) for assigned projects.

Raleigh, North Carolina, Us

Developed, tested and validated clinical databases (both paper based and EDC systems), received and processed external data, programmed and validated datasets, tables, listings, and figures according to sponsor and Kendle requirements and good programming practices to produce the expected results with minimal errors. Responsible for sending datasets, tables, listings, and figures to sponsors within project timelines and for the coordination, creation and maintenance of Scientific Programming project documentation. Validated/performed quality control on programs, ensuring that output meets quality standards and project requirements.

Raleigh, North Carolina, Us

Reviewed and processed clinical trial data to ensure the accuracy and consistency of clinical databases. Commonly performed the following data related activities: CRF tracking, reviewing, validation, updating, SAE reconciliation, lab data reconciliation and safety coding. Responsible for providing accurate, timely, and consistent clinical data to both sponsors and other internal departments to support the business needs of Kendle. Participated in the training of Clinical Data Associates and reviewed/generated ad hoc listings, reports and quality control documentation to facilitate validation of the clinical database.

Highland Heights, Ky, Us

Managed all projects and laboratory operations conducted in The Water Research Laboratory including utilization of databases, billing, budgeting and purchasing and supervision of undergraduate student research. Performed analysis and interpretation of data including graphical analysis and statistics, as well as preparation of reports and presentations.

Masters, Information Systems

Bachelors, Biological Sciences

Bachelors, Environmental Sciences