New Jersey Pharmaceutical Resumes from MedJump.com

Bindya Gadhia - jersey city, NJ

Wed, 18 Jan 2012 19:12:34 -0700

Job Target: Drug Refulatory affairs Associate
Category: Pharmaceutical
Posted: 2012-01-18
Employment Status: Unemployed - Actively Looking
Experience Level: Entry Level
Degree: Master's Degree (MA/MS/MBA)

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Dr. of Pharmacy with Pharmaceutical Industry Experience - Sparta, NJ

Mon, 05 Dec 2011 07:16:46 -0700

Job Target: Entry level pharmaceutical industry position
Category: Pharmaceutical
Posted: 2011-12-05
Employment Status: Employed - Actively Looking
Experience Level: Entry Level
Degree: Doctorate (PhD/MD/JD)

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MBA, MSN, BSN, RN - Lyndhurst, NJ

Sun, 13 May 2012 17:15:28 -0700

Job Target: Drug Safety/PV
Category: Pharmaceutical
Posted: 2012-05-13
Employment Status: Employed - Will Consider Right Opportunity
Experience Level: Mid Level
Degree: Master's Degree (MA/MS/MBA)

Objective: Skilled Health Care Professional with experience in the field of internal medicine and drug safety seeks a challenging position in drug safety.

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Jasmine Cotes, LPN - Haledon, NJ

Fri, 27 May 2011 12:45:34 -0700

Job Target: LPN
Category: Pharmaceutical
Posted: 2011-05-27
Employment Status: Employed - Will Consider Right Opportunity
Experience Level: Entry Level
Degree: Associate or Vocational Degree (AA/AS/MCSE/etc.)

Objective: Seeking a position in the Pharmacovigilance field that will further my experience in the pharmacuetical field. As well as provide me with excellent compenstion and a pleasent work enviorment.

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Sales Dir - Mahwah, NJ

Fri, 25 Jun 2010 17:11:27 -0700

Job Target: Sales manager
Category: Pharmaceutical
Posted: 2010-06-25
Employment Status: Unemployed - Actively Looking
Experience Level: Senior Level
Degree: Master's Degree (MA/MS/MBA)

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timothy cyberey-2 - voorhees, NJ

Tue, 18 May 2010 09:09:56 -0700

Job Target: medical writer
Category: Pharmaceutical
Posted: 2010-05-18
Employment Status: Unemployed - Actively Looking
Experience Level: Senior Level
Degree: Bachelor's Degree (BA/BS)

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franks resume - North Arlington, NJ

Fri, 22 Jan 2010 08:45:54 -0700

Job Target: sales
Category: Pharmaceutical
Posted: 2010-01-22
Employment Status: Active
Experience Level: Senior Level
Degree: Bachelor's Degree (BA/BS)

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Regulatory Affairs Executive - - Monmouth JN, NJ

Sun, 17 May 2009 07:42:52 -0700

Job Target: Marketing & Regulatory Affairs Executive
Category: Pharmaceutical
Posted: 2009-05-17
Employment Status: Active
Experience Level: Not Specified
Degree: Not Specified

Objective: To pursue a career in Regulatory Affairs by leveraging my pharmacy and Regulatory Affairs Certification knowledge skill

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Drug Safety - Bridgewater, NJ

Tue, 21 Apr 2009 09:32:22 -0700

Job Target: Unspecified
Category: Pharmaceutical
Posted: 2009-04-21
Employment Status: Unspecified
Experience Level: Not Specified
Degree: Not Specified

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Reulatory/QA - Associate/Specialist - Lake Hiawatha, NJ

Wed, 18 Feb 2009 04:21:58 -0700

Job Target: Reulatory/QA - Associate/Specialist
Category: Pharmaceutical
Posted: 2009-02-18
Employment Status: Employed - Will Consider Right Opportunity
Experience Level: Not Specified
Degree: Not Specified

Objective: PUNAM DESAI 23 Wenonah Avenue; Lake Hiawatha, NJ 07034 862-812-3835 punam_a_desai@yahoo.com QUALIFICATIONS OVERVIEW Diversified 5 years experience in pharmaceutical, nutritional, and academic industries. Good written and verbal communication skills. Demonstrated ability to organize, prioritize assignments, and meet timelines. Highly flexible and adaptable to changing priorities. Knowledge and ability to use computer technology. EDUCATION MS, Analytical Chemistry, Montclair State University, Montclair, NJ 2004 Distinguished Achievement; Placed #1 in the Comprehensive MS, Physical Chemistry, S.G. University, India 2001 (Equivalent to United States M.S Degree granted by World Education Services, NY) BS, Chemistry, S.G. University, India, 1999 PROFESSIONAL DEVELOPMENT RAC (Regulatory Affairs Certified), RAPS, 2008 Building Better Work Relationships: New Techniques for Result-Oriented Communication, 2008 Qualified cGMP Auditor, 2007 Training for Effective Technical Writing, 2005 Trained on Computer based applications, such as Trackwise, Excel, MS Word, Power point, etc. REGULATORY SKILLS AND KNOWLEDGE ï IND, NDA, and ANDA submissions for drugs and biologics according to CFR Title 21 ï Medical device and combination products submissions ï 510(k) and PMA requirements ï Amendments and Supplements ï RX-to-OTC switch and cosmetics products requirements ï Knowledge of CTD/eCTD format ï Advertising, labeling, and promotional labeling requirements according to Federal Trade commission (FTC) and federal food, drug & cosmetic act (FD&C act) PROFESSIONAL EXPERIENCE Barr Pharmaceuticals, Pomona, NY 2005 ñ Present, Analytical Research and Development Chemist-II 2004 ñ 2005, Analytical Research and Development Chemist-I ï Write method validation protocols and reports as well as investigation/deviation reports in GXPharmaÆ - a completely paperless document management system. ï Involved with Regulatory Compliance department about investigation/deviation (CAPA) actions, Non-conformances, further planning, and method validation & submission related activities. ï Write stability reports and comparative reports for submission of ANDA projects. ï Review test method and Quality Overall Summary report (QOS). ï Participate in method transfer and change control activities. ï Audit documents for method validation and process validation, as well as specification sheet for QA-release and stability testing. ï Perform method validations of USP/NF and non-compendial generic pharmaceutical products in accordance with internal Standard Operating Procedures (SOP) and ICH guidelines. ï Interact with the formulation department to develop and evaluate ongoing ANDA projects. ï Work independently and as a team member in the ongoing ANDA projects to develop and evaluate analytical methods. ï Proficient in literature searches to facilitate product development procedures. 2003 ñ 2004, Montclair State University, Montclair, NJ Graduate Assistant Teacher ï Taught laboratory classes; full responsibility for preparation and delivery of lectures, grading reports, quizzes and exams. ï Established lab assignments; performed calculations, solutions and calibration of instruments; provided extra tutoring during office hours. 2002, Garden State Nutritional, Inc., Fairfield, NJ Quality Control Chemist ï Involved in OTC drugs and dietary supplements testing. ï Analyzed herbal, water-soluble and fat-soluble vitamins. AFFILIATION Member of Regulatory Affairs Professionals Society Member of American Chemical Society

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Regulatory Affairs - jersey city, NJ

Mon, 26 Jan 2009 10:19:55 -0700

Job Target: Regualtory Affairs Associate
Category: Pharmaceutical
Posted: 2009-01-26
Employment Status: Active
Experience Level: Not Specified
Degree: Not Specified

Objective: To secure a position as Regulatory Affairs Associate in Pharmaceutical industries to enrich career and flourish knowledge in regulatory science.

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Pharmaceutical scientist with more then 2 years of experience - JERSEY CITY, NJ

Fri, 23 Jan 2009 01:09:21 -0700

Job Target: Unspecified
Category: Pharmaceutical
Posted: 2009-01-23
Employment Status: Active
Experience Level: Not Specified
Degree: Not Specified

Objective: Enthusiastic and hard working professional. Work effectively alone or as part of a team, benefiting my colleagues with my professionalism and dedication to completing tasks to the best of my abilities. Working for a Pharmaceutical company would be an ideal way to combine my knowledge obtained from my graduation and post graduation studies and the skills obtained during the professional experience.

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Regulatory Operations with 3 Years Experience - Jersey City, NJ

Sat, 08 Nov 2008 13:52:29 -0700

Job Target: Quality Management
Category: Pharmaceutical
Posted: 2008-11-08
Employment Status: Active
Experience Level: Not Specified
Degree: Not Specified

Objective: A highly motivated candidate seeking a challenging Regulatory Operations Position in a growth oriented organization which offers diverse job responsibility.

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chemist - Plainsboro, NJ

Wed, 09 Jan 2008 12:23:16 -0700

Job Target: chemist
Category: Pharmaceutical
Posted: 2008-01-09
Employment Status: Unspecified
Experience Level: Not Specified
Degree: Not Specified

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Entry-level Chemist - Dover, NJ

Fri, 02 Feb 2007 10:54:49 -0700

Job Target: Chemist
Category: Pharmaceutical
Posted: 2007-02-02
Employment Status: Employed - Will Consider Right Opportunity
Experience Level: Not Specified
Degree: Not Specified

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chemist, FTIR, NMR, UV-Visible, HPLC, AA,SEM/EDX - Newark, NJ

Wed, 17 Jan 2007 06:23:52 -0700

Job Target: chemist, scientist
Category: Pharmaceutical
Posted: 2007-01-17
Employment Status: Employed - Will Consider Right Opportunity
Experience Level: Not Specified
Degree: Not Specified

Objective: R&D, QC/QA,formulation Chemist, Scientist ------------------- Qualifications ------------------- - Analytical Instrumentation skills: Optical Microscopy, FTIR, NMR, UV-Visible, HPLC, Atomic Absorption and Cyclic Voltammetry. - Skilled in Scanning Electron Microscopy & Microanalysis techniques. - Good understanding of Mass Spectrometry, GC/LC-MS, and Raman Spectroscopy. - Experienced in organic and inorganic synthesis techniques, including controlled atmosphere glove box conditions. - Working experience in GMP environment.

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2119 Resume - jersey city, NJ

Sun, 06 Aug 2006 02:11:50 -0700

Job Target: formulations
Category: Pharmaceutical
Posted: 2006-08-06
Employment Status: Unspecified
Experience Level: Not Specified
Degree: Not Specified

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Seeking a challenge and opportunity in pharmaceutical/biotech sector that leverages my knowledge of pharmaceutical & healthcare delivery industry with excellent leadership, computer technology, interpersonal and organizational skills. - Branchburg, NJ

Mon, 20 Mar 2006 09:02:10 -0700

Job Target: CRA, CDM
Category: Pharmaceutical
Posted: 2006-03-20
Employment Status: Employed - Will Consider Right Opportunity
Experience Level: Not Specified
Degree: Not Specified

Objective: PROFESSIONAL EXPERIENCE Full-Time: Nurse, Medical Oncology, Robert Wood Johnson University Hospital ñ present Direct nursing care provider to adult oncology patients and their families using standard and Phase III/IV leading-edge oncology treatment protocols. Full-Time: Project Manager, Merck & Co., July 2000 ñ February 2003 In charge of the Corporate headquarters financial & reporting enterprise systems with total annual budget of $2.5 Million. Responsible for leading a team of technical staff in the functional requirements specifications, information architecture, general and detailed design, development, implementation, support, enhancements and integration with external business partners for the comprehensive web applications portfolio. Pioneered numerous division-wide process improvement initiatives, including implementation of Vantive CRM for application defect tracking and resolution management, gaining 30% reduction in support costs within 4 months, deployment of Rational Clear Case/Quest for change control and release management. Full-Time: Schering-Plough Pharmaceutical Co., May 1992 ñ July 2000 Overseeing wide range of Phase III/IV clinical trials application development and support initiatives for Sales & Marketing, Drug Safety & QA, New Drug Development and Drug Information Services clients. Project Leader, Clinical Trials Management From concept to implementation CTMS system in use by 40+ Oncology Biotech CDMs & CRCs in Phase III/IV and post-clinical trials. The system provides competitive marketing advantage by shortening the drugs-to-market cycle and annual cost savings $40 Million. Ensured systems compliance with FDA regulations: GCP, CFR Part-11, HIPPA compliance, ADE/safety reporting and reconciliation. TQA Liaison, Drug Information Services (DIS) Leading a team of internal resources/external consulting firm thru a successful full SDLC effort of a decision support system with $1.2 Million total development budget. The DIS System streamlined drug inquiry-response workflow of phone/written requests from the healthcare professionals, internal field sales force reps. and layman to the drug information specialists in the respective therapeutic areas. ï 21 CFR Part 11 features included: user authentication, provisions for multiple user roles, intrusion detection and lockout, data integrity & audit trails, electronic signatures, electronic systems and user documentation, validated decision support trees, drug information workflow management, and imaging/document management for custom and standard response letters. ï Integration with MedLine and CancerLit databases for literature search and easy mail-merge. ï Integration with internal Regulatory and Drug Safety departments for ADE/safety reporting. EDUCATION/CERTIFICATIONS: B.S., Computer/Life Sciences, University of Pittsburgh, cum laude B.S. Nursing, University of Medicine & Dentistry of NJ, summa cum laude, valedictorian R.N., State of New Jersey, active license, BCLS certified Numerous professional seminars and training in project management, strategic resource management, public speaking, information technology and clinical research. AWARDS AND HONORS: National College Honors List, 2005 Inaugural Ambassador for the UMDNJ School of Nursing

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Clinical Data management - Princeton, NJ

Mon, 31 Oct 2005 02:10:56 -0700

Job Target: Clinical Data Coordinator
Category: Pharmaceutical
Posted: 2005-10-31
Employment Status: Unspecified
Experience Level: Not Specified
Degree: Not Specified

Objective: paddu424@yahoo.com

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Clinical Research * Research/Development Scientist - North Brunswick, NJ

Tue, 19 Jul 2005 04:29:53 -0700

Job Target: Biomedical Quality Control Technologist
Category: Pharmaceutical
Posted: 2005-07-19
Employment Status: Active
Experience Level: Not Specified
Degree: Not Specified

Objective: * Analytical researcher and data management specialist with proven success achieving top operational performance and information accuracy within high-pressure and deadline-driven environments. * Effective in the gathering, administration, storage, testing, and processing of laboratory samples. * Highly detailed-oriented and focused on achieving assignment completion on time and in compliance with operating procedures, standards, and safety regulations. * Maintain FDA-GMP / QSR and ISO standards. * Trained in Phlebotomy, CPR, and First Aid.

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Clinical Data Coordinator - Paramus, NJ

Sat, 11 Jun 2005 01:04:46 -0700

Job Target: Clinical Data Coordinator
Category: Pharmaceutical
Posted: 2005-06-11
Employment Status: Unspecified
Experience Level: Not Specified
Degree: Not Specified

Objective: Looking for a job in a Pharmaceutical/ CRO location Hina Maniar Hinany@yahoo.com 448, Abbott Road 201 265 8591, 201 403 7987 Paramus, New Jersey,NJ 07652 Objective I have a strong desire to obtain a position in clinical setting working independently or with a team oriented environment utilizing my strong written and verbal communication, analytical and interpersonal skills, along with my attention to detail and high organization skills. Qualifications Certifications  Completed CRA certification and training - from Medical Research Management institute (CRTI).  Completed the HIPAA course  Knowledge of medical and clinical research techniques in Oncology. I have 6 months experience as a Clinical data coordinator and looking to find a opportunity as a CRA. I am handling 12 studies in Oncolgy from companies like Bristol Myers Squibb, Novartis, Pharmion and ECOG. Education 1993 Ph D in Immunology from Cancer Research Institute (Bombay University) 1985 M.Sc in Microbiology (Bombay University) 1981 Bachelors in Microbiology (Bombay University). Current Position: 2005-Clinical Data Coordinator at Hackensack Medical Center. Responsibilities: Maintenance of study documentation according to study protocol and FDA regulations:  Timely serious adverse event (SAE) reporting.  Preparedness for monitor/audit visits.  Organized and accurate source/CRF documentation.  Maintain FDA/IRB documentation including: 1572, informed consent and CVs. Maintain timely submissions of screening logs, enrollment logs, and referral logs. Assure compliance with all FDA regulations and company procedures. I perform proper source documentation, data collection, drug accountability, lab specimen collection, and lab processing for all trials to maintain high quality data output.  Assist in the preparation of clinical study summary reports  Help to coordinate clinical studies, provide data verification, and assist in preparation of clinical summaries.  Collect, process, and track regulatory documentation as required by the FDA regulatory association.  Liaison with data coordinators at CRO sites. Other duties as assigned. Transferable competency requirements:  Communication skills (written, verbal, non-verbal)  Customer service (subjects, sponsors, co-workers)  Time management/efficiency  Working with teams  Safety  Problem solving Specific technical competency requirements:  Computer skills (MS Office and associated modules, Word, Excel, Power point and Internet) Work History Projects Undertaken and Responsibilities: 2003-2004 Sr. Research Associate, Phase I clinical trials and vaccine production under cGMP and preclinical Development .Memorial Sloan-Kettering Cancer Center, Gene Transfer and Somatic Cell Engineering Facility, New York. 1998-2002 Research Fellow, Memorial Sloan Kettering Institute, New York. 1995-1997 Research Associate, Rutgers University, New Jersey. 1993-1995 Research Fellow, Centrum for Bioteknic, NOVUM, Karolinska Institute, Sweden 1989-1993 PhD course work. 1992-1993 Scientific Officer B, Cancer Research Institute, Bombay, India. Professional Courses  Successfully completed the cGMP training from Sloan Kettering Institute .  Attended a audio conference series on Computer Validation in the Cell Therapy laboratory, 2004. It defines the basic requirements for validation of computer system, lists important elements of part 11 and how these elements affect cell therapy laboratory databases, explains validation issues and critical elements of an inventory management systems. Additional Certifications  Successfully completed the regulatory affairs credit course from CSUH. These courses in regulatory Affairs cover;  Overview to the laws governing development, manufacture and commercial distribution of drugs, biologic and medical device products(FDCA), and  Studies of current Good Manufacturing Practice regulations to assure quality of marketed products, application to manufacturer's organization, personnel, facilities, equipment, control systems, production, process controls, laboratory procedures and records (21 CFR 210, 211, 610 and 820, cGMPs- US FDA and EMEA, FDA and ICH regulations related to biologics). References Publication list and references will be available upon request

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eNV. CHEMIST W/15 YRS EXP. - EAST BRUNSWICK, NJ

Wed, 11 May 2005 00:23:49 -0700

Job Target: cLINICAL dATA COORDINATOR
Category: Pharmaceutical
Posted: 2005-05-11
Employment Status: Unspecified
Experience Level: Not Specified
Degree: Not Specified

Objective: OBJECTIVE: To obtain a challenging position where dedication and interpersonal skills as an associate Data Coordinator, including data validation, electronic data management and technical knowledge, will contribute to the overall success and growth of the company. EDUCATION: B.S. in Microbiology/Chemistry, Ahemdabad Science College, INDIA,1985 Client/Server-Compu-Learn, Edison, NJ ñ1998 Introduction to Drug Development, Clinical Data Management Skill Course ñ 10-11/2004 Barnett International -The Clinical Research Team Overview of CDM -Protocol Design and Development -Case Report form Design and Development -Data Tracking and Collection Methods and Data Entry -Data Review, Validation, and Data Queries -Medical Terminology and Coding -Quality Control/Quality Assurance and Data Reporting -Database Release and Biostatistics -Adverse Experience Reporting and Reconciliation -Remote Data Capture STATUS: U.S. CITIZEN CERTIFICATIONS:  Inorganic Data Validation USEPA Region II-1990  Organic Data Validation USEPA Region II-1991  40 Hrs Hazardous Waste Training, Roy F. Weston, 1991  Certified in Quality Assurance and Field Sampling analysis-1993  Completed Client/Server course. Learned programming concepts, Database programming in Oracle 7. x, SQL server and application development in Visual Basic 6.0 COMPUTER SKILLS: Client/Server-1998 Microsoft Office (Word, Excel, Power point, Access), Internet Explorer 4.0/5.0/5.5, Windows NT/95, Lotus Notes. PROFESSIONAL EXPERIENCE: Quality Assurance Officer, RST Contract September 2000 - Present Weston Solutions, Inc. Edison, New Jersey Responsible for the review and completeness of QAPPs, conducted periodic timesheet audits. Responsible for all facets of the procurement process from identifying needs to file maintenance. Solicited and evaluated bids and ensured that all analytical services were procured in compliance with federal and WESTON procedures. Issued Purchase Orders through ORACLE and Cost Point Purchasing System. Obtained certificates/soil permit for shipments from foreign sources through any U.S. port of entry. Assisted team members to choose appropriate screening techniques and determine sampling methods for the various situations and sites. Maintained and supported case tracking database activities and non-CLP database. Prepared weekly and monthly status reports for the client. Trained technical staff in data validation and helped project managers and field personnel in CLP sample management procedures. Analytical Service Coordinator, START Contract September 1995 - August 2000 Roy F. Weston, Inc. Edison, New Jersey Performed the key QA functions of Contract Laboratory program (CLP) and Data Validation coordination for all projects for EPA Region 2 in support of Superfund activities. Reviewed and validated more than 600 organic and inorganic analytical data packages. Used EPA Standard of Work protocols, revalidation, verification, and qualification checks of validated materials generated by regional contractors and technical reports. Summarized data review findings. Maintained and supported case tracking database activities and non-CLP database. Prepared weekly and monthly status report for the client. Trained technical staff in data validation and helped Project Managers and field personnel in CLP sample management procedures. Assisted the START II Team Manager in the preparation of weekly and monthly reports for the client. Analytical Service Coordinator, TAT/ESAT Contract June 1992 - September 1995 Roy F. Weston, Inc. Edison, New Jersey February 1988 - February 1991 Performed Organic and Inorganic data validation in accordance with USEPA Region II data validation protocol in support of the Technical Assistance Team(TAT) contract. Worked closely with USEPA-Monitoring Branch personnel to improve and facilitate data validation process. Project Manager February 1991- June 1992 ICF Kaiser Engineers, Inc. Iselin, New Jersey. Responsible for the direct supervision of five chemists, report writing and reviewing, and overseeing final deliverables. Prepared and evaluated Request for Bids for the subcontracting of environmental services. Performed Organic and Inorganic data validation in accordance with USEPA Region II data validation Analytical Chemist July 1987 - February 1991 Chemtech Consulting Group New York, New York. Assembled and performed qualification check of CLP data packages generated by analytical group. Scheduled work assignment and reported completed data packages to clients and Conducted experiments in a wet-chemistry laboratory.

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Sales Representative 3 years expierence - Bradley Beach, NJ

Wed, 28 Jul 2004 08:50:49 -0700

Job Target: Unspecified
Category: Pharmaceutical
Posted: 2004-07-28
Employment Status: Active
Experience Level: Not Specified
Degree: Not Specified

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Clinical Data Manager - Elizabeth, NJ

Fri, 28 May 2004 03:51:53 -0700

Job Target: Clinical Data Manager
Category: Pharmaceutical
Posted: 2004-05-28
Employment Status: Active
Experience Level: Not Specified
Degree: Not Specified

Objective: To obtain a challenging position where I can utilize my studies in Clinical Data Management

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Clinical Research - Newark, NJ

Sat, 24 Jan 2004 13:07:26 -0700

Job Target: Clinical Research Coordinator
Category: Pharmaceutical
Posted: 2004-01-24
Employment Status: Active
Experience Level: Not Specified
Degree: Not Specified

Objective: SUMMARY OF QUALIFICATIONS: Excellent leadership skills; highly motivated, positive and enthusiastic team player Professional attention to detail Working knowledge of International Conference on Harmonization guidelines (ICH) and Good Clinical Practice standards (GCP) Adept at working under pressure; qualified and trained to handle multiple tasks successfully Advanced computing skills in Microsoft Word, Excel, Access, PowerPoint, FrontPage, SPSS, MOCHA and Financial Records System (FRS) with ability to learn and use new software Fluent in English and Indian languages (Hindi, Marathi, Gujarati) EDUCATION: Master of Healthcare Administration, Seton Hall University, NJ...August '03 (Courses studied include Research Methods and Descriptive Statistics, Financial Management, Healthcare Financial Management, Strategic Planning and Healthcare Economics) Bachelor of Dental Surgery, Kolhapur University, India...May '00 PROFESSIONAL EXPERIENCE: Clinical Research Coordinator, Pulmonary Medicine, Newark Beth Israel Medical Center, NJ...September '03- present Screen, enroll and follow-up potential study subjects in accordance with the study protocols and regulatory guidelines Facilitate study visits by sponsors and monitors Perform study related tests and laboratory work like spirometry, EKG, clinic sample preparation Ascertain all FDA and IRB policies are met Intern, Pre-Edit Department, Delta Dental Plan of NJ...September '02 ñ September '03 Identified and audited claims, x-rays and attachments based on audit guidelines to be approved or routed to dental consultants Assisted in training new associates for the Pre-Edit Department Assistant Budget Manager and Data Analyst, Center for Public Service, Seton Hall University...January '02 ñ May '03 Managed partial annual departmental budget of $10,000 and was in charge of purchasing supplies Student Course Evaluations: Analyzed and reported approximately 200 student evaluations per semester Analyzed and reported all data from prospective, current and graduating students as part of the National Association of Schools of Public Affairs and Administration Assessments (NASPAA) Student recruitment: Organized and coordinated graduate recruitment fairs on campus and off-site Dental Intern at Government Dental College and Hospital, Bombay, India...August '00 - July '01 Performed simple and complex dental procedures and surgeries Conducted seminars and trained undergraduate students Coordinated and assisted professors in lecture series Conducted dental camps in rural areas REFERENCES: Available on Request

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