Aarohi Bhatt, Doctor of Pharmacy (PharmD)
ac8eez@r.postjobfree.com
ac8eez@r.postjobfree.com
* ******** **** ***. ** Fords, NJ 08863
PharmD professional with effective communication and organizational skills seeking a suitable position
4 years’ combined academia and pharmaceutical research analysis experience in the Biochemistry, Molecular biology, and Oncology along with Doctor of Pharmacy EXPERIENCE
Research Analyst- Healthcare, Amneal Pharmaceuticals, NJ June 2018-Present
Conceptualized in business strategies, promotion and advertising of a drug and biological products
Diagnose issues and provide results-focused recommendations for life science/ pharma partners across the areas of:
o Strategy and portfolio analysis
o Brand/commercial strategy
o Pricing and market access
Establish report templates and document management within SharePoint
Effectively communicate with medical associates to reconcile GATM records with proper documentation
Attended KOL talks, biotech conferences, and held meetings with several financial experts
Analyzed and performed clinical diagnostics in conjunction with an ongoing clinical trial
Developed and presented several investigational protocol reviews at clinical trial meetings
Performed single stock analysis of biotechnological marketed products
Interpreted financial analysis based on current market trends
Researched on drug development and company ventures based on their pipelines
Strong expertise in communication across multidisciplinary research teams, vendors and business professionals with non-scientific background
Utilized databases such as Medidata, RAVE, and reviewed clinical literature along with latest research on pharmaceutical products
Expert at data analysis and visualization using GraphPad Prism, Excel, and Flow Jo to ensure the safety and efficacy of the trial design; programming data structures using SDTM, Optum
Maintained distribution lists and scheduled travel, meetings, and handled expense reports
Understanding of ICH guidelines, ISO 9001, ISO 13485
Thorough knowledge of Chemistry, Manufacturing and Controls (CMC)
Proficiency in Medical devices, IDE, 510 (k) submission, PMA, Quality System Regulation, CE marking
Familiarized with FDA submission of IND, NDA and ANDA as per (eCTD) format
Understand 21 CFR 314, 21 CFR 314.50, 21 CFR 312, GLP regulations, USP requirements, and FDA guidance Oncology Research Associate, MCPHS University, MA Dec 2014-May 2018
Conduct oncology-based experiments, collect and analyze data in support of long-term project proposal to supervisor and collaborators to advance laboratory research
Assist in managing two different projects across a multidisciplinary collaboration between 4 laboratories by allocating funds, resources and distribution of responsibilities
Studied the effect of different drug treatments alone or in combination through in vitro cell based assays like PCR, site directed mutagenesis, DNA cloning
Testing of different anti-cancer therapies alone or in combination in the tumor model in vivo through sub- cutaneous injections
Presented scientific findings at international oncology conferences, student post doc symposium and department seminars
Mentor research technicians, undergraduates and graduate students in experiment planning, use of best laboratory practices, troubleshooting and data presentation
Work specifically in novel targeted drug delivery using in vitro models of human cancer cell lines; lung cancer
Prepare nanoliposomes of lipids and the drug Doxorubicin using rotary evaporator
Seed and culture the 48 well plate to check the cell cytotoxicity using the SRB protocol
Prepare liposomes and determine their zeta potentials and particle sizes
Grow, split, and perform experiments on various cancer cell lines
Check cellular uptake of cancer cells using rhodamine and perform fluorescence intensity
Plot the cell cytotoxicity and IC50 graph using Prism® software
Develop various schematics using professional ChemDraw® software Quality Assurance Associate, Amneal Pharmaceuticals, NJ March 2014-Aug 2014
Inspected products for quality, operational accuracy and suitable site monitoring for such products
Assured proper documentation for production audits and packaging components
Inspected samples to ensure procedure followed according to SOPs, cGMP and FDA regulations, review of inventory card and issuance of documents
Monitored of packaging process and reconciliation of packaged products
Reviewed environmental data of processing rooms and stability chambers for ensuring compliance to cGMP and SOP's
Submitted raw material samples for testing to QC and Analytical labs SKILLS AND RELEVANT COURSEWORK
Advanced Biochemistry, Gene Technology, Neurophysiology, Developmental Biology, Accounting, Creating and Growing a Business Venture (Series 87, Series 86, Series 63, Series 7: In Progress)
Skills: Statistical Analysis, Market Research, Discounted Cash Flow, Revenue Modeling, MS Excel, Outlook, PowerPoint
EDUCATION
Doctor of Pharmacy (PharmD) Sept 2015-May 2018
Massachusetts College of Pharmacy and Health Sciences, MA. GPA - 3.8 Bachelor of Pharmacy May 2008-May 2012
Gujarat Technological University, India. GPA - 3.89 HONORS AND AWARDS
MCPHS University, MA
Phi Lambda Sigma Society in Pharmacy May 2016-May 2018 Dean’s List May 2015-May 2018
VOLUNTEER AND ENTREPRENEURIAL EXPERIENCE
Vice President, American Society of Hospital Pharmacists May 2016-May 2018
Actively involved in conducting monthly events including fundraising, community services, and various professional learning events for PharmD students throughout the year