D inal Gandhi
*** ****** *, *** ***, Bayonne, NJ 07002
E-mail: *********@*****.***
O bjective:
A highly motivated, team oriented, clinical research professional with a strong
u nderstanding of the Clinical Research field. Additional skills include planning and
executing clinical studies and maintaining compliance with Good Clinical Practice (GCPs),
S tandard Operating procedures (SOPs), and study protocol seeking a career opportunity in
C linical Research field where my skills and experience can be utilized to add value to the
business and the team.
Education:
Rutgers University Newark, NJ
• Masters of Science in Regulatory Affairs (Anticipated M ay -2016)
Campbell University Buies Creek, NC
• Bachelors of Science in Clinical Research A ugust 2005-August 2008
Skills:
• Knowledgeable with Medical Terminologies along with FDA regulation relevant to
clinical t r ials, good clinical practices and Standard Operating Procedures (SOPs)
• Academic experience with descriptive statistics, hypothesis testing, and other
s tatistical methods
• Hands-on experience with M icrosoft Office and Power Point
• Working experience with Data entry and managing data in MS Excel and MS Access
Databases
• Knowledgeable with organization, collection, review and t racking of data
• Academic experience with Drug Development through the course work
• Working experience with clinical t r ial methodology during internship
• Proven project management skills to efficiently manage multiple projects and
resources resulting in t imely project delivery within predetermined budgets.
• Working experience in the maintenance of clinical t r ial study files and records
• Working experience in medical and scientific research environment
I n te rnships
Duke University Medical Center (OB/GYN Depart) Durham, NC
C linical Research Assistant January 2008 – April
2008
• Assisted Principle Investigators(PIs) on four clinical research studies such as
administrative work and research related activities
• Created CRFs (Case Report Form) and performed data entry
• Maintained study documentation, patient clinical information and regulatory
b inders for clinical studies
• Knowledgeable of clinical t r ial regulations to ensure compliance adherence.
• Conducted medical literature researches and prepared papers for publications
• Collaborated as an active member of the research team
Volunta ry Activities
Massachusetts General Hospital, (Boston, MA) November 2010 – March
2011
Research Assistant at Edwin L. Steele, Laboratory
• Assisted research fellow on breast cancer related research
• Working experience with suturing process and cell culture techniques
• Assisted fellow in Immunohistochemistry protocol
• C reated protocol to implant tumor cells into mice using different techniques
Work Experience:
CVS Pharmacy - Bayonne, NJ December 2011
- P resent
Certified Pha rmacy Technician
• Supported CVS’ “MY CUSTOMER PROGRAM” by delivering excellent customer
support resulting in increased sales.
• Created customer profiles for “new” customers and assisted in preparation of
p rescriptions for pick-up within planned tu rn around t ime.
• Perform daily updates of the client’s profile in the CVS database in support of
customer service initiatives.
P ha rmaceutical Research P roject C ampbell
U niversity
R esearch Assistant J une 2007 – Dec
2007
• Used nine nonprescription analgesic products in solid dosage forms
• Solid units were pulverized with a porcelain mortar and pestle and then
i ncorporated into a cocoa butter base for formulating the suppository
• The Journal of Pharmacy Technology: Suppository Preparation: Density Factor
Determination for Some Over-the-Counter Analgesic Products was published.
References
Available upon request