Heather D. Email & Phone Number

Arlington, Tx, Us

Arlington, Tx, Us

Tampa, Fl, Us

West Chester, Pa, Us

Leads cross-functional teams including the CRO in the delivery and success of clinical trials, overseeingclinical monitoring activities throughout the entire trial lifecycle and ensuring strict adherence to monitoring standards, protocols, and project deliverables.Demonstrated exceptional proficiency in orchestrating the implementation of start up, maintenance andoperations, and close-out for research projects, strictly following the guidelines outlined in the scope of work and project plan.Maintains accurate internal systems, databases, tracking tools, timelines, and project plans with attention to project-specific details, enabling streamlined data management, timely decision-making, and accurateforecasting and reviews.Strategically implemented risk management and preventive action plans, identifying potential challengesearly in the trial, and proactively implements solutions.Effectively led project communications with key stakeholders, fostering collaborative relationships whileimplementing comprehensive KPIs to enable data-driven decision-making, ensuring efficient escalation andresolution of issues, and enhancing trial performance and quality to achieve strategic objectives.

Fort Worth, Texas, Us

Mentor and develop a team of clinical research staff, ensuring their professional growth, while effectivelycoordinating and delegating responsibilities, resulting in improved team performance and successfulexecution of clinical trials.Created comprehensive SOPs, study-specific templates, communication plans, and training of staff thatimproved operations, enhanced site compliance, and effectively supervised investigator site files,investigational product management, and source data verification.Showcased proactive initiative in juggling competing priorities and guaranteeing on-time deliverables,maintaining an optimistic outlook and delivering top-notch work performance in a fast-paced environment.Demonstrated exceptional accuracy and attention to detail in maintaining clinical trial documentation,including forms, patient records, and essential regulatory documents, ensuring compliance with industrystandards.

Dallas, Tx, Us

Successfully coordinated and managed the execution of multiple complex clinical trials simultaneously,ensuring accuracy and adherence to protocols, strict timelines, budgetary constraints, and regulatoryrequirements, resulting in the timely completion of high-quality studies.Adhered to core values in everyday conduct, contributing to a positive and supportive work environment for the entire team.Actively engaged in process improvement initiatives, contributing to the optimization of supply chainmanagement and procurement processes to streamline trial operations.

Independently managed all aspects of clinical research operations, overseeing multiple trials simultaneously while exhibiting exemplary organization and attention to detail.Single-handedly handled financial responsibilities, including budgeting, invoicing, and expense tracking, ensuring accurate financial reporting and cost-effective trial execution.Successfully streamlined processes, implementing efficient protocols and optimizing resource allocation to achieve maximum productivity while maintaining a strong focus on quality and compliance.

Medical Assistant Certification, Medical Assistant

High School Diploma