Opportunity for Medical Coder at MakroCare

MakroCare Expert Strategic Development and Commercialization Global Partner for Pharmaceutical, Biotechnology and Medical Device industries. Our Experience, Programs and Processes bring a New Dimension to Development Strategy, Regulatory/Risk Planning & Management, Clinical Research, Medical/Scientific Support and Emerging Region Expansion.

Post : Medical Coder

Job Description
MakroCare is an Expert Strategic Development and Commercialization Global Partner for Pharmaceutical, Biotechnology and Medical Device industries. Our Experience, Programs and Processes bring a New Dimension to Development Strategy, Regulatory/Risk Planning & Management, Clinical Research, Medical/Scientific Support and Emerging Region Expansion.

Main Responsibilities :
• Responsible for Coding Adverse Events and Concomitant diagnosis using the current version of MedDRA as distributed by MSSO and in accordance to the Client specific SOP's.
• Coding of Medical data in a timely manner.
• Ensure Critical studies with consistent coding and handling issues.
• Coordination of import or export of data for coding and transfer of data/coded terms to clients.
• Review listing for coding terms to ensure accuracy and consistency of coded data.
• Consistent with client guidelines and regular checks for feedback's.
• Authenticate accuracy of Terms Processed and maintaining the safety compliance, also ensuring quality standard.
• Documenting the observations on an internal generated Quality check sheets (quality control form, defect tracker).
• Providing regular feedback to the team members for continuous improvement of the process.
• Maintain and Update daily metrics.
• To make sure all the priority study terms are processed on priority
• Secondary quality Checks of Serious Spontaneous Adverse Events / Post Marketing adverse event / Clinical trial and invalid terms.
• Maintain knowledge on updates or changes in medical coding dictionary versions.

Candidate Profile
Top primary skills required for this role :
• Good computer skills including but not limited to the knowledge of Clinical Trial/Data Management Systems, knowledge of MS-Office products such as Excel, Word.
• Sound awareness of all relevant regulations, including GCP.
Secondary skills required for this role:
• Ability to organize and plan tasks
• Shows commitment to and performs consistently high quality work
• Excellent interpersonal, verbal and written communication skills.
• Sense of urgency in completing assigned tasks.
Tertiary skills required for this role:
• Plans and delivers verbal and written communications that persuade the intended audience.
• Sense of urgency in completing assigned tasks.
Any other specifications:
• Should have experience in leading the projects and able to communicate to client directly whenever required.

Additional Information
Experience : 1 to 3 years
Location : Hyderabad, Telangana
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Medical Coder
End Date : 2/14/2020

Contact Person : Rajesh Neelam
Contact Email : talent.hr@makrogrp.com