Experience

CSSi

• United States
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Site Monitor/Patient Recruitment Specialist

  • Sep 2016 - Present

  • Collaborate with study coordinators to meet the recruitment needs of their site • Coordinate community outreach events • Develop recruitment plans that are site specific • Organize and host meetings for physicians and their colleagues • Assist with recruitment advertising strategies • Manage recruitment activities for 30+ sites • Compose and execute sales strategies to meet the company goals • Collaborate with study coordinators to meet the recruitment needs of their site • Coordinate community outreach events • Develop recruitment plans that are site specific • Organize and host meetings for physicians and their colleagues • Assist with recruitment advertising strategies • Manage recruitment activities for 30+ sites • Compose and execute sales strategies to meet the company goals



Cognitive Solutions

• Washington D.C.

• Psychometrist

  • Aug 2015 - Sep 2016

  • Administered neuropsychological assessments • Evaluated the cognitive development of patients • Composed neuropsychological reports • Completed administrative tasks • Administered neuropsychological assessments • Evaluated the cognitive development of patients • Composed neuropsychological reports • Completed administrative tasks



Howard University

• United States
• Higher Education
• 700 & Above Employee

• Clinical Research Coordinator

  • Jun 2011 - 2015

  • Recruited and consented individuals into drug and non-drug related clinical trials • Administered neuropsychological assessments • Completed data entry • Coordinated multiple studies with over 80 or more participants • Conducted genetic disclosure visits • Administrated neuropsychological and transcranial exams • Completed quality control of binders • Monitored subjects’ vitals • Completed IRB regulatory submissions for clinical trials • Recruited and consented individuals into drug and non-drug related clinical trials • Administered neuropsychological assessments • Completed data entry • Coordinated multiple studies with over 80 or more participants • Conducted genetic disclosure visits • Administrated neuropsychological and transcranial exams • Completed quality control of binders • Monitored subjects’ vitals • Completed IRB regulatory submissions for clinical trials