Clinical Research Assistant/Clinical Research Coordinator

OBJECTIVE

Seeking a challenging position in research field which enables me to utilize my knowledge and experience and also learn and grow.

CAREER PROFILE

•Proficient in medical terminology

•Involved in patient care including medical histories, vital signs, diagnostic, evaluation of test results and administration of treatment procedures, and preventive health care services

•Good Knowledge in Good Clinical Practice, HIPAA, OSHA, writing Standard Operating Procedures, Creating Inventory forms and Consent forms

•Excellent clinical and analytical skills and a quick learner

•Involved in administrative support such as answering telephones, assisting visitors.

•Exceptional record maintenance skills

•Immense ability to schedule appointments and maintain calendars

•Involved in scheduling meetings for all employees, escorts visitors to staff member’s offices, along with provides hospitality service arrangements

•Skilled in using Microsoft Office, Word, Outlook and Excel software

•Excellent organizational, interpersonal, verbal & written communicational skills.

•Effective team player yet able to work independently

•Ability to work in challenging environments highly motivated, very hard working and determined to succeed

EXPERIENCE

Biometrix (UCSF affiliated), San Francisco, CA.

Clinical Research Project Coordinator Nov 2007 – 2008

•Estimated budget for the study and determined feasibility for company.

•Set up a plan to execute the study

•Created advertisements and posted them for the accepted studies.

•Recruited and enrolled subjects, collected study data, and managed all logistical aspects of study

•Completed an initial patient assessment utilizing interview and observation

•Verified documentation of the informed consent process for each study subject

•Monitored that the physician adheres to study protocol

•Obtained Vital Signs, monitored participants labs and taught proper procedures to patients

•Intervened and recommended patient needs and/or changes as appropriate to the PI and other health professionals

•Created required Inventory forms of supplies

•Created and updated the Log sheets for the lab

•Experienced in clinical supplies packaging, labeling and distribution of clinical trial materials

•Received and shipped appropriate study supplies

•Ensured all study related supplies are available prior to study.

•Ensured filing and maintenance of the required regulatory

documents (investigator's study and regulatory binder, source

documents and CRFs)

•Ensured adverse events were properly documented and reported.

•Assigned and oversaw tasks and managed the clinical trial to a

successful completion

South Asian Heart Center (El Camino Hospital), Mountain View, CA. Health Risk Assessment Consultant (Volunteer) Sept 2007 – Present

•Responsible for general office work and data entry

•Co-coordinated Health fair

•Manage documents, to recruit and enroll subjects

NTR University of Health Sciences, India

Internship

•Interned in Medicine, Surgery, Orthopedics, Pediatrics, Ophthalmology, E.N.T, Obstetrics and Gynecology including family welfare, Community medicine, Skin and Venereal disease, Casualty, Psychiatry

•Examining inpatients in wards and outpatients-Taking their vital signs, chief complaints, history and diagnosing the disease, make relevant lab requests and giving them the required treatment

EDUCATION

•Michigan State University

Clinical Research Monitoring and Coordination Course – Present

•Bachelor of Medicine and Bachelor of Surgery (M.B.B.S)

Grade-Second Class

Course work - included Anatomy, Physiology, Biochemistry, Microbiology, Pharmacology, Pathology, Ophthalmology, Otolaryngology, Medicine, Dermatology, Psychiatry, Surgery, Orthopedics, Obstetrics and Gynecology, Pediatrics, Social and Preventive Medicine.

VISA STATUS

•US Citizen

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