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All Skills

Project Administrative Assistant

Marlton, NJ
... Clinical Study Specialist Develops, evaluates, and executes all essential clinical trial documents, budgets, and clinical trial agreements (CTAs). Aligns execution activities with agreed upon project priorities, timings and quality specifications. ... - Apr 21

Manager Data

Peru, Pisco, Ica
... lab and diagnostic tests, CTCAE toxicities, clinical research references, and an integrated chemotherapy-specific clinical decision support . Maintain a database of all clinical trials; enter trial details, eligibility, contract information, ... - Apr 21

Project Manager

Piscataway Township, NJ
... 2012 Cmed Research Clinical Trial Administrator • Support the clinical research team with ongoing conduct of studies • Assist project teams with study specific documentation as appropriate • Prepare study-specific procedures, study newsletters, etc. ... - Apr 19

Medical Quality

Los Angeles, CA
... and Diagnostics - Introduction to Medical Product Regulation - Quality Systems and Standards - Management of clinical trials - Clinical Trial Design and Statistic - Medical Product Law - Chemical Manufacturing Controls - Pre-clinical studies - ... - Apr 16

Customer Service Data Entry

Bushkill, PA
... Process and maintain electronic and paper clinical trial documentation. . Support project teams initiatives with filing, scanning, and archiving. . Identify and resolve documentation discrepancies with various departments. . Review, reconcile and ... - Apr 15

Quality Control Data Entry Office Manager Experience

Kensington, MD
... Mar 2009 – Apr 2010 Clinical Data Management Associate II, Oncology Cmed, Inc New Providence, NJ Reviewed clinical trial documents (e.g. protocol, validation document and Electronic Case Record Forms) and provided input as appropriate; maintained ... - Apr 12

Data Management

India, New Delhi, DL
... Ltd - Bangalore Mar 2009 - Mar 2012 Clinical SAS Programmer - Pharmacokinetics 0. Creation of datasets and quality check of raw data using SAS 8.0. 0. Analysis and reporting of trial data (like demographic, adverse events and concomitant medication) ... - Apr 11

Customer Service Medical Device

Kansas City, MO
... Clinical Disclosure Agreement, Investigator Agreement, Clinical Trial Agreement) to sites and updating these essential documents in the Impact. • Upload and track Site Protocol Deviation Issues in SPDR. • Assists in ensuring adherence to applicable ... - Apr 10

Medical Management

India, New Delhi, DL
... It was a premier institute for professional training programs as M.sc in Clinical Research, Clinical Data Management, Clinical Trial Management, and Advanced Post Graduate Diploma's in Clinical Research, Pharmacovigilance, Medical Writing, ... - Apr 10

Data Quality Assurance

Raleigh, NC
... Knowledge of the drug development process with strong experience of analyzing and reporting in phase I, II and III of clinical trial data. . Thorough knowledge of Clinical Trials data like Demographic data, Vital Signs, Adverse Events (AE), ... - Apr 08

Project Manager Customer Service

United Kingdom, London
... Assisting in overseeing compliance and documentation related to receipt, storage, dispensing/accountability of clinical trial supplies and non-study drugs. Overseeing return of supplies to sponsor or their destruction. . Preparing annual turnover ... - Apr 06

Quality Assurance Data Entry Management Safety

United States
... Health and Harrison EDC environments Covance – NASHVILLE, TN 07/05 – 03/12 Clinical Safety Associate -Manage Drug Safety projects -Provide updated CVs and signatures for the trial master files -Answer the drug safety hotline throughout the day. ... - Mar 29

Software Engineer Sql Server Management Project

India, Ahmedabad, GJ
... Ltd, Ahmedabad Tools & Technology VB.Net, Java script, .Net framework 3.5, Sql server 2008 Application Type Web Application Team Size 10 Description: BizNET-CTM is an application for Clinical Trial Management. It provides- Manage all clinical trial ... - Mar 29

Clinical Research Director, Clinical Research Associate, Coordinator

MO
... Complete and maintain regulatory documents • Perform internal quality assurance audits • Perform budget negotiations with clinical trial sponsors and maintain clinical trial financial records • Construct investigator initiated protocols and informed ... - Mar 28

Biostatistics, SAS

Tampa, FL
... Design and Conduct of Clinical Principles of Health Policy and Trial Management Applied Linear Regression Environmental and Occupational Health Categorical Data Analysis Social and Behavioral Sciences Applied to Health PROFESSIONAL POSITION Apr. ... - Mar 25

Experience Assistant Research Data Design Project

New Haven, CT
... for Statistics in Science Research Assistant Prepared SAS macros for verifying the integrity of the patients data from clinical trial • Generate summary tables with descriptive statistics of the variables • Maintained and debugged SAS code using for ... - Mar 21

Regulatory Affairs

Boston, MA
... and REMS materials ) - Provided regulatory support to global clinical trials group * Worked closely with the Contract Research Organization (CRO) to manage and track multiple global clinical trial applications for four clinical trial programs in US, ... - Mar 20

Manager Management

Boston, MA
... Managed the development of commercial regulatory and clinical applications (Clinical Trial Management, EDMS, Drug Safety Systems, Product Complaint Management) . Developed software documentation and testing methodologies to meet client and FDA ... - Mar 19

Quality Assurance Medical Device

United States
... (Formerly Abbott Laboratories) J uly 2012- Present Chicago, I L Position: Global Regulatory Affairs Associate • Prepared and complied RA- HCV- Clinical Trial Application Dossier for two medicinal products for Regulatory submission in China, Korea ... - Mar 19

Manager Accounting

Union City, CA
... • Set up multiyear and multiphase government or clinical trial contract schedules. Trace and report related cost to statutory agencies. • Maintain Great Plains software and custom-design reports to make it more efficient. • Biotech and clinical ... - Mar 19

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