Designation Regulatory Associate Fresher opening Parexel

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Careers Save this JobApply Button will redirect you to recruiters resume management system Report this job Apply here PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Perceptive Informatics, Inc., a subsidiary of PAREXEL, provides advanced technology solutions, including medical imaging, to facilitate the clinical development process. Headquartered near Boston, Massachusetts, PAREXEL operates in approximately 70 locations throughout over 50 countries around the world, and has more than 13,000 employees. At PAREXEL, we have a passion for making a profound difference. As an expertise-based business, the caliber of our people and their dedication directly impacts our success, the success of our clients, and the ability to make a difference in the lives of patients worldwide. You"ll be surrounded by supportive leadership and a brilliant team who share a common goal - to improve the lives of millions of patients Designation Regulatory Associate Job Description ESSENTIAL DUTIES AND RESPONSIBILITIES: include the following. Other duties may be assigned. Perform publishing readiness activities including: Troubleshoot and fix format and style issues in MS Word documents to ensure submission readiness standards. Perform submission readiness activities including: Prepare PDF source documents, including intra-document hyperlinks and bookmarks, Page rotation and PDF optimization. Perform electronic publishing activities including: Assign source documents to electronic publishing outlines. Enter metadata. Prepare to publish and publish output. Create inter-document hyperlinks and bookmarks. Perform paper publishing activities including: Scan and make submission ready paper documents. Create tables of contents, tables of figures and tables of tables. Split PDF output into appropriate volume sizes. Assign navigation aids such as: tabs overlays and pagination. Convert legacy documents to relevant electronic or paper output. Format and publish simple reports and submissions. Perform basic document management tasks including file transfer, storage, tracking, and archival. Maintain familiarity with current global regulatory submission standards. Maintain familiarity with departmental standard operating procedures and work instructions. Desired Profile Bachelor's degree or equivalent in life sciences or technology-related discipline. 0 to 4 years experience; or equivalent combination of education and experience. Experience 0 - 4 Years Industry Type Pharma / Biotech / Clinical Research Role Team Lead/Technical Lead Functional Area IT Software - Other Education UG - Any Graduate PG - Any Postgraduate DOCTORATE - Doctorate Not Required Location Bengaluru/Bangalore Keywords Regulatory AssociateTroubleshootmetadata Contact HR PAREXEL International (India) Pvt Ltd Website http://www.parexel.com Job Posted 12 Dec Reference 10030166 Save this JobApply Button will redirect you to recruiters resume management system Report this job