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Vimmikumari K Patel

59 Paterson Ave,

Hoboken, NJ 07030 1- 917-330-5810

professional Objective

To obtain a position that will utilize and challenge my knowledge & skills in pharmacology & toxicology, quality control & quality assurance, drug development process including interpersonal communication, leadership and technical competence, to meet organizational objectives.


  • Quality Control & Quality Assurance

  • Research & Development

  • Pharmacology & Drug development process

  • Clinical Pharmacology & Clinical Research Studies


Long Island University, NY. GPA: 3.80/4.0

Master of Science in Pharmacology & Toxicology (May 2010)

University of Pune, India. GPA: 3.99/4.0

Bachelor of Pharmacy (July2006)


Clinical Research Associate

Care Worldwide Inc., New York, NY. (May 10 – Oct.2010)

  • Monitoring all safety issues and continuous site monitoring as well as site evaluation.

  • Overseeing all Clinical Trial activities before, during the project and at study close out.

  • Obtaining ICF from volunteer for screening and study and data entry into CRF (Case Report Form).

  • Monitoring screening process and preparation of study related document through site assessment and evaluation.

  • Monitoring of clinical study to ensure that study is conducted in compliance with the protocol and the Good Clinical Practice (GCP).

  • Protocol, Informed Consent Form and Case Report Form preparation

Quality Control Analyst

Asian Drugs & Pharmaceuticals, Gujarat, India. (Aug.06 – Jan.07)

  • Documentation and Batch Manufacturing Records maintenance in accordance with cGMP guidelines.

  • Analyzing, reviewing and developing strategies pertaining to material control and quality data system.

  • Quality control tests pertaining to tablets and capsules viz. hardness, dissolution, disintegration, friability etc.

  • Hands on experience in managing and handling laboratory instruments as well as proper maintenance and documentation.

  • Managing Quality Control logs and records for proper adoption of standard operating procedures.

  • Assisting in documentation for validation of laboratory instruments, processes and equipments for FDA Inspection.

Unimark Remedies Ltd; India (May 05 – Aug. 05)

  • Worked as trainee in manufacturing, quality control and packaging department.

  • Extensive training related to basic concepts of c-GMP pertaining to quality control and quality assurance.

  • Regulation practices (ICH, FDA), in manufacturing department.

  • Maintaining batch manufacturing records for the department.

Sadna Kutir Pharmacy (May 04 – July 04)

  • Volunteered work in the store for Dispensing over the counter medicines.

  • Training about maintaining inventory of the stores.

  • Training for maintaining regulatory aspects of the stores.


Toxicology of drugs and chemicals, Principles of Immunotherapy, Autonomic pharmacology, Biochemical Pharmacology, Molecular Pharmacology, Molecular Toxicology, Advanced Pharmacology, Pharmacogenomics, Experimental Pharmacology, Cardiovascular Pharmacology, Inborn errors of metabolism.


  • Fourier Transform Infrared Spectroscopy (Perkin Elmer Spectrum v5.3.1 software)

  • UV/Visible Spectroscopy

  • High Performance Liquid Chromatography

  • In Line Refractometers

  • High Performance Thin Layer Chromatography

  • Conductivity meter and Ultrasonicator


  • Platforms: Windows XP, Vista, Windows 7 MacOS X.

  • Applications: MS-Word, MS-Excel, MS-PowerPoint, Adobe Photoshop.

Reference(s) available upon request.