IQVIA is seeking a Clin Data Coder 2 to join their team in Bengaluru, India. In this role, you will provide expertise in clinical data management (CDM) and coding activities, supporting clinical trials through the study life cycle. The position allows you to serve as a Lead Coder or Coding Reviewer, as well as manage coding projects and customer relationships, ensuring quality coding practices and effective project delivery.
Essential Functions and Responsibilities
As a Clin Data Coder 2, your key responsibilities will include:
- Independent Coding Leadership: Act as a Clinical Data Coder, Lead Coder, or Coding Reviewer for one or more projects, ensuring high-quality coding deliverables.
- Customer Relationship Management: Manage client interactions, particularly around coding timelines, budgets, and project-related issues.
- Project Management: Oversee the full life cycle of coding activities, from planning and execution to ensuring the quality and consistency of coding deliverables.
- Coding Application and Report Testing: Validate coding applications and the programming of coding reports, as well as testing coding-related datasets.
- Process Improvement: Identify areas for improvement in coding processes and contribute to continuous improvement initiatives.
- Collaboration and Stakeholder Communication: Work with cross-functional teams to address issues, escalations, and roadblocks, and develop solutions for better project outcomes.
- Quality Control: Perform rigorous quality control procedures on coded data and ensure that coding activities meet high standards.
- Documentation and Reporting: Participate in the development, revision, and maintenance of standard operating procedures and work instructions for coding tasks.
- Adherence to Protocols: Ensure compliance with study protocols, regulatory standards, and industry best practices in clinical data management and coding.
Qualifications
To be considered for the Clin Data Coder 2 role, you will need:
- Educational Requirements: A degree in Pharmacy, Dental, Medical, Nursing, Life Sciences, or a related field.
- Experience: At least 4 years of relevant experience in clinical trials, with a focus on clinical data management and coding. Experience in data management or a similar function is also required.
- Medical Coding Knowledge: Expertise in Medical Dictionaries used for coding (e.g., MedDRA, WHODD, ICD9, etc.) and a solid understanding of medical terminology, pharmacology, anatomy, and physiology.
- Project Management Skills: Knowledge of project management principles and the ability to manage all phases of clinical studies.
- Drug Development Understanding: A comprehensive understanding of the drug development process and the role of data management within it.
- Technical Proficiency: Familiarity with database technologies related to data management and coding. Strong computer skills, with a working knowledge of relevant software tools.
- Communication and Leadership Skills: Excellent organizational, written, and verbal communication skills in English, with the ability to lead teams, resolve conflicts, and foster collaboration.
Preferred Skills and Qualifications
- Ability to manage project timelines and resources effectively.
- Knowledge of coding-related edits and programming activities.
- Strong attention to detail and independent problem-solving capabilities.
- Experience in conflict resolution, delegation, and team leadership.
