Senior Data Coding Specialist (Thiruvananthapuram)

Worldwide Clinical Trials; Thiruvananthapuram; On-site; INR 500,000 - 800,000; Full time

Job summary

Worldwide Clinical Trials in India, Kerala, seeks a Clinical Coding Specialist to code adverse events, medical histories, and medications using sponsor dictionaries and maintain dictionary versions. This role supports project coding activities, participates in study start-up coding on existing and new EDC databases, and backs up the Manager Clinical Coding and Data Management as required.

The successful candidate will follow SOPs and coding guidelines and contribute to high-quality data for

Qualifications

• Experience in coding medical and surgical terms.
• Familiar with coding guidelines and sponsor dictionaries.
• Ability to perform data management testing and UAT.

Responsibilities

• Provide coding support for projects, including coding for adverse events, medical histories and medications.
• Coding activities for study start up on existing and new EDC databases.
• Input into the Data Management Plan and perform User Acceptance Testing, including review of database specs and CRFs.
• Perform manual coding of medical and medication terms, generation and review.
• Back up to Manager Clinical Coding and Data Management as required.

Job description

Who we are

Were a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the worlds most persistent diseases is not paved by those who play it secure. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

Join us

SUMMARY: Utilize standard and/or sponsor custom dictionaries to code Adverse Events, Medical and Surgical Histories, Medications and any other sponsor requested medical terminology required for projects. Ensure coding guidelines and company SOPs are adhered to and dictionary versions / updates are maintained as appropriate for the project. Back up to Manager Clinical Coding and Data Management as required.

RESPONSIBILITIES

Tasks may include but are not limited to:

• As a priority, provide coding support for projects including:
• Coding activities for Study start up on existing and new EDC databases
• Input into the Data Management Plan, performing User Acceptance Testing, including review of Database Specifications and CRFs
• Performing manual coding of medical and medication terms, generation and review .
• Back up to Manager Clinical Coding and Data Management as required.