The Team
Who We Are
Dr.Ashish Anand
Child, Adolescent and Adult Psychiatrist
In my work as a psychiatrist and a therapist I have tried to help my patients. While there is a role for medication management, therapy can help patients to both understand the context in which their symptoms arise, and to learn useful coping strategies. I am board certified in Child/Adolescent and Adult Psychiatry, completed my fellowship at New York Presbyterian Hospital (where I served as Chief Resident), both my medical school and residency training were in Boston (Boston Medical Center/ BU School of Medicine), and I earned my BA from NYU, graduating Magna Cum Laude.
I am open to meeting for a consultation. I also offer 2nd opinion consultations and upon request, take on a limited number of medication management only cases where patients are already connected with their own therapist.
My other area of interest is research. As a psychiatrist I see 1st hand both the promise and limitation of current medication treatments. As a researcher working on clinical trials for psychotropic medications, I hope to advance both our current knowledge base and treatment options available to our patients.
201-378-3011
Dr.Palika Anand
Research Administrator and Lead CRC
I graduated from Ross University School of Medicine. I have extensive experience in clinical research both as a Clinical Research Coordinator (CRC) and Clinical Research Associate (CRA).
In my role as a CRC, I coordinated psychiatric clinical trials focusing on conditions such as adult, ADHD, and binge eating disorder. I effectively recruited participants through advertising campaigns, assessed eligibility via phone screenings, and closely with the research director to evaluate protocol feasibility. I coordinated with CROs for all monitoring visits, sponsor audits and all interim visit requests, acted as primary liaison between IRBs, sponsors and CROs including Medical Monitors and Project Managers and provided regulatory compliance in line with GCP/ICH, Internal Review Board, sponsor, and CRO specifications.
As my role as a CRA,I was Internationally Qualified Clinical Research Associate (F-IAOCR) and was responsible for monitoring all types of clinical trials, assures adherence to Good Clinical Practice, investigator integrity and compliance with all study procedures. My primary responsibility is for site management and performance, including documentation, site management activities include all in-house and on-site monitoring for all visit types.
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201-632-1496
