Tenacious and skilled management professional with 15 years of experience running clinical trials, public health research, epidemiology, and corporate training. Outstanding ability to drive transformative change by developing training programs, software implementations and adoption, protocol development, and standardized documentation, reshaping program productivity and culture. Proven impact in managing complex trials (HIV/AIDS, TB, Hepatitis, and Oncology). Gifted speaker and motivator, excelling in engaging presentations and speeches while fostering strong team dynamics. Recognized for a positive attitude, boundless energy, and proactive approach to problem-solving and inspired by the opportunity to bring new drugs to market, previously collaborating with the NIH and CDC in East Africa.
Current Whereabouts:
I have a solid background in clinical trials. I recently authored the book "Beyond Barriers: Diversity Action Plans, A Roadmap for FDA Compliance," which addresses community engagement strategies to reduce health disparities in diverse communities. This work demonstrates my deep commitment to equity and access for all people.
Life & Professional Aspirations:
My life aspiration is to establish wellness centers in underserved communities around the world to improve health outcomes and close disparity gaps.
Founded the Seeds of the Diaspora, an organization focused on bridging the cultural gaps and promoting African awareness among people of African Descent. SGA Sophomore Class Secretary and member of the GSU Royal Court Ms. Junior 1997. Earl Lester Cole Honors College and Magna Cum Laude Graduate.
Most Memorable Moment:
Helping raise money and awareness for GSU men to attend the Million Man March in Washington DC. Joining the Distinguished Women of Delta Sigma Theta Sorority.
Consultant |
Pinnacle Planning Associates
From January 2024 to Current • 2 year(s)
I lead cross-team projects that aligned business goals with partners, resulting in successful biotech and institutional collaborations. I designed an innovative observational study protocol using AI to address Breast Cancer in high-risk and minority populations in both the US and Africa. Additionally, I launched a virtual health channel aimed at educating diverse communities and improving health outcomes. I also developed clinical trial training programs that significantly boosted client efficiency and cultural competence. My role included providing digital consultation to design websites and social media content, which enhanced client engagement and outreach.
Regional Vice President Partner|
Primerica Inc
From January 2021 to May 2024 • 3 year(s)
As a Regional Vice President Partner at Primerica Inc., I led a team of State and Federal licensed trainers, educating consumers on financial tools and programs to establish secure fiscal plans. I supervised and trained a salesforce of 10 direct and 60 indirect licensed agents across 10 states, handling all aspects of their development from hiring and orientation to classroom and field training, as well as ongoing mentorship. I managed a substantial portfolio of over 250 investments, with Assets Under Management exceeding $6.9 Million, and average monthly life insurance premiums of $6.2 Million. Through innovative training and motivational leadership strategies, I achieved a 25% increase in team productivity and elevated our sales to the top 10% tier in the USA. My performance was recognized with induction into the President's $100,000 Club in 2013 and the Distinguished African American Leadership Council in 2017. I also oversaw administrative and compliance activities, including regulatory audits, ensuring 100% adherence to federal and state laws, resulting in clean data audits annually.
Project Manager |
Thermofisher Scientific
From June 2020 to December 2020 • 0 year(s)
As a Project Manager at Thermofisher Scientific, I spearheaded 10 projects from initiation to close, overseeing all aspects of project management including planning, quality control, budgeting, data evaluation, ROI analyses, and final reviews. My comprehensive approach ensured timely milestone delivery and strict adherence to project roadmaps. I meticulously assessed project parameters and client engagement, tracked milestones, mitigated risks, and managed expenses, which resulted in a 15% reduction in project delays and a 10% increase in client satisfaction. Additionally, I managed contract negotiations and compliance for over 55 outside contractor agreements, overseeing expenses and invoicing for 40 contractors. This diligent oversight led to a 20% reduction in contract disputes and significantly improved cost-effectiveness across our projects.
Senior Clinical Research Associate|
Covance
From April 2014 to December 2016 • 2 year(s)
As a Senior Clinical Research Associate at Covance, I championed 10 successful clinical trials, leading project teams and overseeing all aspects of the research process. My responsibilities included monitoring clinical data, directing CRO and sponsor meetings, conducting experiments, screening participants, making observations, tracking results, and analyzing data. I ensured all experiments met clinical practice and safety standards, implementing efficient recruitment tools and participant screening methods that achieved a 10% reduction in clinical trial start-up timelines. I meticulously analyzed and managed clinical source documents, reviewed Informed Consent (ICF) and Trial Master File (TMF) documents, and prepared Clinical Trial Agreements and regulatory documentation for phase II and III oncology trials. By closely monitoring active studies to verify compliance with protocols and Good Clinical Practice (GCP) standards, I maintained a 100% compliance rate. Additionally, I implemented 10 Corrective Action and Preventative Action (CAPA) Plans, ensuring adherence to GCP and Good Manufacturing Practice (GMP) standards, which resulted in a 15% improvement in investigator satisfaction.
Clinical Trials System Manager |
AstraZeneca (MedImmune)
From June 2006 to October 2011 • 5 year(s)
As a Clinical Trials Systems Manager at AstraZeneca, I championed program oversight, leading five clinical, software implementation, process improvement, and change management projects from initiation to closing. I built new project business cases and gained buy-in, resulting in a 25% increase in operational efficiencies and a 40% improvement in data quality. I spearheaded a complete overhaul of the Clinical Trial Management System (CTMS), implementing four new solutions including eClinicalWorks, eSource Systems (RAVE), IVRS, and XRS. Leading a team of 20 stakeholders through testing, training, and adoption, I achieved a substantial $10 million cost reduction and established a fully interoperable system.
My role involved analyzing, tracking, documenting, and mitigating project risks, identifying root causes, and maintaining open communication with sponsors, stakeholders, and the project team. I supervised the design and implementation of clinical strategies, monitoring plans, and CRA Site Monitoring Reports in CTMS, while also managing study updates to Clinical Development protocols. Leveraging my data analysis skills, I examined process and performance data from clinical study datasets and documents, implementing solutions that resolved over 30 complex process issues.
I established comprehensive project documentation, including protocol worksheets, procedural manuals, and Clinical Study Reports (CSRs). By pinpointing project milestones and areas for improvement, I ensured on-time project completion and achieved a 15% boost in project team productivity. Throughout my tenure, I consistently utilized best practices in CTMS implementation, ensuring regulatory compliance, data security, and efficient clinical trial operations.
International Biomedical Research Training Program|
National Institutes of Health
From May 1998 to September 1998 • 0 year(s)
I worked as an Research Assistant investigating HIV/AIDS and Kaposi Sarcoma Herpesvirus in Kampala Uganda.
