Dependable and accomplished professional with extensive healthcare, research and medical experience. Highly skilled in clinical research management, recruitment and education of multiple clinical trials. Skilled in working under pressure and adapting to new situations and challenges to best enhance the patient outcome. Excellent reputation for resolving problems, managing multiple priorities and eager to improve patient care. Versatile clinical research professional that is knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Knowledgeable and adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues.
CSM responsible for management, compliance, quality and profitability of multiple Phase 1 Clinical Trial Studies, focused on drug-drug interaction, food-drug interaction studies, MAD-SAD studies, etc.
Accountabilities:
CTE for Diabetic Macular Edema, a Phase 1 multi-center study to evaluate safety, pharmacokinetics and pharmacodynamics of GSK212669 after 28 day repeat oral administration to adults with Diabetic Macular Edema.
CTE for MultiStem Administration for Stroke treatment and enhanced recovery study (MASTERS-2)- a Phase 3 study to examine the safety and effectiveness of the allogenic, adult stem cell investigational product, MultiStem, in adults who have suffered an acute ischemic stroke in the previous 18-36 hours. Managed 13 sites involved in this study located across the United States.
Accountabilities :
Involved in a variety of administrative tasks to support investigators and ensure the smooth running of clinical trails and assist with collecting patient data.
Accountabilities:
Accountabilities :
2015- 2016
2014
2011- 2012
2014 - 2018
2015 - 2016
2014
2010- 2012
2012- 2014
2011- 2012
2015
2014
2011- 2012