Robert Trott Email & Phone Number

Specializing in clinical monitoring of Phase I-IV clinical trials. Offers support from site selection, Initiation, routine monitoring, and close out visits to Project management, Drug accountability, Patient accrual, regulatory compliance, and report preparation. Fields of expertise consist of women’s health (Osteoporosis), CNS (OCD, Anxiety, Depression.

Responsible for monitoring and managing clinical sites for i3Research clients. Therapeutics areas included ADHD, Diabetes, and Vaccine.

Contracted with Pfizer Central research, Groton, CT. Responsibilities include Monitoring CNS, diabetic, and womens health clinical trials. Inspecting site records and documents, ensuring accuracy and completeness; monitor study drug supplies ensuring proper accountability; provide site investigator and coordinator direction as necessary to ensure valid and.

Responsibilities include inspecting site records and documents, ensuring accuracy and completeness; monitor study drug supplies ensuring proper accountability; provide site investigator and coordinator direction as necessary to ensure valid and safe studies and to resolve problems; ensure compliance with FDA and company requirements; examine numerical and.

Responsibilities include inspecting site records and documents, ensuring accuracy and completeness; monitor study drug supplies ensuring proper accountability; provide site investigator and coordinator direction as necessary to ensure valid and safe studies and to resolve problems; ensure compliance with FDA and company requirements; examine numerical and.

Bs, Research Psychology\Business Administration

Worked full time to put myself through college.

Education record