Clinical Research Medical

VIJAY PARIKH, CCRC

Torrance, CA • 310-***-****/562-***-****

*************@*******.***

SKILLS

Certified Clinical Research Coordinator with 11 years of clinical research experience overseeing all aspects of clinical trials

Superior project management skills and demonstrated ability to oversee several clinical studies simultaneously

Extensive experience coordinating with program staff and pharmaceutical company representatives, while conducting face-to-face consultations with patients and maintaining databases and reports

THERAPUETIC EXPERIENCE

Circulatory: Hypertensive, Hyperlipidemia, & Cardiovascular

Endocrine-Metabolic: Diabetes: Type I & II and Blood Glucose Meters

Dermatology: Acne, Psoriasis

Respiratory: Asthma and COPD

KEY ACCOMPLISHMENTS

Managed six to seven studies per year, including studies of asthma, COPD, hypertension, pediatric vaccines, diabetes, ADHD, psoriasis, cholesterol and acne and atopic dermatitis.

Led and coordinated over 25 studies for various cosmetic products and procedures.

Conducted all aspects of clinical trials, including recruiting, screening and enrolling patients

(including scheduled and recorded patient visits), while maintaining records and CRFs.

Managed sites participating in multi-center clinical research trials, Phases 2-4.

Provided study coordination including screening of potential patients for protocol, eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.

Create protocol format and consent format for principal investigator and submit it to IRB for approval.

Worked with diabetes study for phase 2 and phase 3 study from 2006 onwards, many protocol using new devices and extensive blood testing for follow up during study VIJAY PARIKH, CCRC

Torrance, CA • 310-***-****/562-***-****

*************@*******.***

PROFESSIONAL EXPERIENCE

Applied Biomedical July 2015- Current

Clinical Research Site Monitor

General guidelines for recruitment, screening and enrolling patients with record maintenance

Device clinical study for diabetes meter, contract for 1 month only

Trained site staff for the protocol and protocol related procedures

Provided study coordination including screening of potential patients for protocol, eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.

Long Beach Clinical Trials Center, Long Beach, CA Mar 2015 - Current Clinical Research Coordinator

Setting up of clinic trial center for research activity including subject’s privacy, consent process, document recording, I.P. Storage facility

Contacting pharmaceutical/ CRO for study feasibility.

General guidelines for recruitment, screening and enrolling patients with record maintenance

Updating clinic procedures as per GCP and Clinical Research requirements

Framework of source documents including templates for research and clinic use

Create SOP format and consent format for site usage

AND successfully starting studies

Encino Research Center, Encino, CA Sep 2013 – Feb 2015 Clinical Research Coordinator

Managed six to seven studies per year, including studies of psoriasis, cholesterol and acne and atopic dermatitis.

Led and coordinated over 15 studies. Conducted all aspects of clinical trials, including recruiting, screening and enrolling patients (including scheduled and recorded patient visits), while maintaining records and CRFs.

Managed site participating in multi-center clinical research trials, Phases 2-4.

Provided study coordination including screening of potential patients for protocol, eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.

Trained site staff for the protocol and protocol related procedures

QM (QC and QA) implementation for dermatology studies Peninsula Research Associates, Inc., Rolling Hills, CA May 2004 – Aug 2013 Clinical Research Coordinator

VIJAY PARIKH, CCRC

Torrance, CA • 310-***-****/562-***-****

*************@*******.***

Managed six to seven studies per year, including studies of asthma, COPD, hypertension, pediatric vaccines, diabetes,

Conducted all aspects of clinical trials, including recruiting, screening and enrolling patients

(including scheduled and recorded patient visits), while maintaining records and CRFs.

Managed site participating in multi-center clinical research trials, Phases 2-4.

Provided study coordination including screening of potential patients for protocol, eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.

Private Medical Practice (Pediatric), Mumbai, India Pediatric Medicine

Examined, diagnosed and administered treatment to pediatric patients.

Maintained extensive patient contact. Monitored patients to track follow-up visits, collected and recorded data from patient visits.

Supervised staff of pharmacists and nurses.

EDUCATION AND CERTIFICATIONS

Mumbai University, Mumbai, India

M.D. (Pediatric), 1982

ACRP

Certified Clinical Research Coordinator, 2006 – Present University of California, Long Beach, CA

Coursework in Master of Public Health (2004)

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