Parexel International Hiring Experienced Clinical Data Coder @ Hyderabad

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Job Description

Job Title    Clinical Data Coder

Job Family    Data Management

Requisition #    pare-10038313

India – Andhra Pradesh – Hyderabad

Why Work at PAREXEL  
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.

Job Description  

The role of the Clinical Data Coder (CDC) is to independently perform all clinical data coding activities on assigned projects, commensurate with experience and/or project role.
Responsible for coding a moderate to large study or multiple small size protocols as a CDC Coder, with minimal to no supervision. Alternatively, take on the role of a Clinical Coder on smaller projects.

Previous relevant Coding experience and technical knowledge preferred, or data management, clinical and / or research experience with solid understanding of clinical trials methodology and terminology
•Bachelor’s degree in Science concentration and / or other medical qualification or relevant DM experience


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