WhatsApp Group Join Now
Telegram Group Join Now

ad
AD

Johnson & Johnson

5 years

5 - 14 Lacs per Year

Mumbai/Bangalore/Hyderabad

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

johnson & Johnson (J&J) is a global leader in healthcare and pharmaceutical products. With a strong commitment to improving the health and well-being of people worldwide, J&J operates in over 60 countries. The company’s work spans consumer health, pharmaceuticals, and medical devices, offering cutting-edge solutions that positively impact lives. In India, Johnson & Johnson continues to innovate and expand, providing employees with dynamic career opportunities in various functions.

Responsibilities in the Analyst II Medical Coder Role
As an Analyst II Medical Coder at Johnson & Johnson, your key responsibility will be ensuring accurate and consistent coding of clinical study data, adhering to J&J’s coding guidelines and regulatory requirements. Here’s a detailed overview of the role’s responsibilities:

  • Oversight and Adherence to Coding Practices: Ensure compliance with Regulatory Authority and Industry standards for data coding practices.
  • Data Coding Execution: Deliver accurate, reproducible coding of clinical trial data while meeting project timelines.
  • Collaboration: Act as a key contributor in cross-functional teams, providing coding support and addressing coding inquiries across sectors.
  • Continuous Improvement: Participate in initiatives aimed at improving coding processes, ensuring consistency, efficiency, and innovation.
  • Thesaurus and Code List Maintenance: Contribute to the upkeep and enhancement of dictionary encoding products and systems.
  • Support Problem Solving: Assist in problem-solving activities, offering solutions to data coding issues under the guidance of senior colleagues.

You will work closely with various functional teams such as Clinical Data Management, Biostatistics, Regulatory Medical Writing, and Clinical Trial Leaders to ensure coding is done accurately and in compliance with all required guidelines.

Qualifications and Experience Required
To be successful in this role, you will need the following:

  • Educational Requirements: A Bachelor’s degree (e.g., BS, BA) or equivalent professional experience is required, ideally in Clinical Data Management, Health, or Computer Sciences. An advanced degree (e.g., Master’s, PhD) is preferred.
  • Experience: At least 5 years of experience in the pharmaceutical, CRO, or biotech industries, with a proven understanding of industry-standard coding thesauri such as MedDRA and WHO Drug.
  • Knowledge of Coding Systems: Experience in utilizing and maintaining coding systems and dictionary encoding products is essential.
  • Communication Skills: Strong written and verbal communication skills in English are crucial to interact effectively across various functions.
  • Multi-functional Experience: The role requires the ability to work in a multi-functional environment and adapt to different workflows.

Preferred Qualifications

  • Knowledge of the drug development process and adherence to GCP/ICH guidelines.
  • Innovative thinking to contribute to the design and execution of medical coding strategies.

Skills Needed
In addition to the technical qualifications, the ideal candidate will possess the following skills:

  • Problem-solving skills: Ability to resolve complex coding challenges with input from senior team members.
  • Collaboration skills: Ability to work effectively with cross-functional teams and external partners.
  • Adaptability: Flexibility to adjust to different working styles and environments.
  • Attention to detail: Precision in data coding and adherence to project timelines.

Application Link

ad
AD

Sticky Buttons
Join WhatsApp Group References Join Telegram