More than * years of experience in clinical research with last 4 years in clinical trial monitoring as a Clinical Research Associate in large multi-national, multicentre studies (phase II and III) carried out by multinational companies. Have significant experience working in Psychiatry and cardiology studies.

Has been monitoring a number of multi-national, multicentre clinical trials in India. Responsibilities span the full duration of studies, from start-up to project close-out. Performed site identification and selection visits in various studies across therapeutic areas like, bipolar depression, acute schizophrenia, Parkinson’s disease, inter-critical gout, COPD, Urology etc.

Have worked with Key Opinion Leader in this therapeutic area. Have worked with many diverse sites scattered all over India. Believe in strong customer service, quality and ethical work. Always achieved timeline during course of study through teamwork, efficiency and planning. Have developed strong therapeutic, technical, communication and cultural skills. Have thorough understanding of principles ICH-GCP, 21CFR and local regulation.

Therapeutic area experience include: (phase II and III pivotal clinical trials)

• Central Nervous System: Acute Schizophrenia, Parkinson’s disease, Anxiety Disorder

• Cardiology: Venous thrombosis (Deep Vein Thrombosis and Pulmonary Embolism, Acute Coronary Syndrome)

• Oncology: metastatic bone pain, Renal Cell Carcinoma

• Rheumatoid Arthritis

• Nephrology: Diabetic Nephropathy

• Gastroenterology: Ulcerative Colitis

• Infectious Disease: Japanese Encephalitis

Over 6 months experience as a trainee clinical pharmacist.

• Undergone clinical pharmacist training (practice based) during master’s program covering various modules such as principles of clinical pharmacokinetics and their application, evidence-based medicine, drug information, patient counselling, case notes and medication review, Therapeutic Drug Monitoring (TDM) of medications such as digoxin, phenytoin, sodium valporate etc., adverse drug reaction monitoring and drug dosage calculation.

• Participated in ward round with physicians and consultants in hospitals and monitoring for drug administration, adverse effects, drug interaction and medication adherence.

Pfizer Limited (In source through Clininvent Clinical Research)

Jan 2011 to Present

Clinical Research Associate for West Region)

ICON Clinical Research

Bangalore, India

June 2010 to Dec 2010

Clinical Research Associate (CRA - II)

Quintiles Research (India) Pvt Ltd.

Ahmadabad

01 Nov 2006 – Mar 2010

Clinical Research Associate (CRA - II)

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