Hyderabad PAREXEL International Corporation Ltd Openings on 23 Nov 2014 Apply Any Graduate
Job Details:
Designation:Senior Clinical Data Analyst
Job Description :
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. PAREXEL 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.
Senior Clinical Data Analyst
- Manage all phases of data management activities from study start up to database close, which may include:
Development of database build specifications
Development of data validation specifications
Test data creation & UAT
Performing/ leading functional QC activities and testing
Create CRF Completion Guidelines (CCG), SAE reconciliation Guidelines, etc.
Data validation and cleaning
Conduct medical coding if assigned
Conduct SAE & third party data reconciliations
Perform early and final database QC activities
Database lock activities
Maintaining Clinical Study Documents and archiving as appropriate
- Responsible for completeness, timely delivery and quality of clinical data
- Lead and coordinate other team members within the department on assigned studies
- Mentor project team members and be a subject matter expert when needed
- Represent DM function in external client meetings and presentations such as investigator meetings as required. May represent PAREXEL at professional meetings / conferences
- Facilitate cross functional team meetings both internally and externally as needed
- Other assigned responsibilities as needed
Must be able to demonstrate proficiency with several tasks included in data start-up through data-base lock. Previous relevant 4 to 7 years data management work experience required with solid understanding of clinical trials methodology and terminology desirable.
Experience:4 - 7 Years
Industry Type:Pharma / Biotech / Clinical Research
Role:Clinical Research Associate/Scientist
Functional Area:Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Education
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