Are you seeking to establish a robust career in clinical data management while working remotely? If you have experience with medical coding, MedDRA, WHODD, and EDC systems like RAVE or Veeva, this opportunity could be the next big step in your professional journey. 🚀
A leading global clinical research organisation is hiring a Coding Specialist (Clinical Data Associate I) for a remote, full-time role based in India. This position enables you to participate in international clinical trials while maintaining a healthy work-life balance.
🧬 About the Role: Coding Specialist (Clinical Data Associate I)
As a Coding Specialist, you will play a critical role in ensuring that clinical trial data is accurate, standardised, compliant, and ready for analysis. Medical coding is a cornerstone of clinical research, directly impacting data quality, regulatory submissions, and patient safety.
This role offers exposure to global clinical trials, collaboration with cross-functional teams, and the opportunity to work with industry-standard coding dictionaries and systems.
🏢 Job Highlights
📍 Location: Remote (India)
💼 Job Type: Full-Time
🧪 Category: Clinical Research / Clinical Data Management
🕘 Work Schedule: Standard (Monday to Friday)
🆔 Job ID: R-01338263
🏠 Work Mode: Fully Remote
🎯 Key Responsibilities
As a Coding Specialist, your day-to-day responsibilities will focus on maintaining high-quality clinical data while adhering to regulatory standards.
🔹 Core Duties Include:
🩺 Coding medical terms using MedDRA and WHODD in line with the study Coding Plan and Data Validation Manual (DVM)
📋 Reviewing coding listings to ensure accuracy, consistency, and compliance
🔍 Identifying data discrepancies and collaborating with study teams and clinical sites to resolve issues
✅ Ensuring all coding activities follow SOPs, GCP guidelines, and departmental procedures
🤝 Providing guidance and support on coding-related matters to the Clinical Data Management (CDM) project team
⏱️ Delivering coding outputs on time, within budget, and with high quality
📊 Preparing project-specific coding status reports for supervisors and clients
🗂️ Maintaining proper documentation to ensure inspection-ready data
This role requires a balance of technical expertise, attention to detail, and strong communication skills.
🎓 Education & Experience Requirements
To qualify for this position, candidates should meet the following criteria:
🎓 Bachelor’s degree or equivalent in a relevant life science or healthcare field
🧪 1 to 1.6 years of hands-on experience in clinical data management or medical coding
💻 Practical experience with RAVE or Veeva EDC systems
📘 Strong working knowledge of MedDRA and WHODD coding dictionaries
📑 Understanding of clinical trial protocols and Data Validation Manuals (DVMs)
🧠 Required Knowledge, Skills & Abilities
Successful candidates will demonstrate the following competencies:
📚 Excellent understanding of clinical and medical terminology
🧩 Strong analytical and problem-solving skills
🖥️ Ability to work efficiently with interactive computer programs and clinical systems
✍️ Clear written and verbal communication with a strong command of English
🔐 Ability to maintain strict confidentiality of medical records and proprietary client data
🎯 High attention to detail and commitment to quality
🤝 Strong interpersonal skills with a customer-focused mindset
🔄 Flexibility and adaptability to work both independently and within a team
🧠 Sound judgment and decision-making abilities
🗂️ Highly organised approach while adhering to global SOPs and regulatory standards
🌟 Why Choose This Opportunity?
Working as a remote Coding Specialist offers several career and lifestyle advantages:
🌐 Exposure to global clinical trials across multiple therapeutic areas
🏠 Work from home with a stable Monday-to-Friday schedule
📈 Career growth in clinical data management and medical coding
🧪 Opportunity to work with top pharmaceutical and biotech companies
🧾 Experience producing inspection-ready, high-quality clinical data
💡 Continuous learning in a fast-evolving clinical research environment
This role is ideal for professionals who enjoy data accuracy, regulatory compliance, and collaborative teamwork.
🚀 Who Should Apply?
This position is perfect for:
Clinical Data Associates is looking to specialise in medical coding
Professionals with MedDRA/WHODD experience seeking remote roles
Candidates aiming to grow within clinical research and CDM functions
Individuals who value quality, compliance, and structured work environments
Apply Now 👇🏻:
https://jobs.thermofisher.com/9oAK7Gb
🔚 Final Thoughts
If you are passionate about clinical research, enjoy working with medical terminology, and want the flexibility of a fully remote role, this Coding Specialist position offers an excellent platform to advance your career. 🌱 With exposure to global studies, standardised systems, and collaborative teams, this role can help you build a strong and future-ready profile in clinical data management.
👉 Start your journey toward a rewarding remote career in clinical research today!
