AGATI CLINICAL INFORMATICS LLP
Location
India | India
Job description
Key Responsibilities:
. Perform accurate and consistent coding of adverse events, medical history, and drug-related information using MedDRA and WHODrug dictionaries and standard coding guidelines.
. Stay updated on the latest versions of MedDRA and WHODrug and ensure coding compliance with regulatory standards.
. Handle standalone coding projects, ensuring adherence to coding guidelines and maintaining data accuracy.
. Conduct historical data coding, reviewing, and coding past clinical trial data to align with current coding standards.
. Collaborate with cross-functional teams to ensure smooth integration of coding processes into overall clinical data workflows.
. Generate coding reports as required for internal and external stakeholders.
. Demonstrate proficiency in using the Medidata Coder tool for coding activities.
. Troubleshoot and resolve coding-related queries and discrepancies, collaborating with technical support when necessary.
. Maintain accurate and up-to-date documentation of coding processes and decisions.
Qualifications:
. Obtained a bachelor's or master's degree in life sciences, pharmacy, nursing, or a related field.
. Proficiency in using coding software and relevant databases.
. Strong attention to detail and accuracy in coding.
. Knowledge of clinical trial processes.
. Excellent communication and teamwork skills.
. Ability to work in a fast-paced and dynamic environment.
Job tags
Salary
