Coding Specialist II

Work set-up: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Bachelor's degree in life sciences, pharmacy, or related field, or equivalent professional certification., Minimum of 3-4 years of experience in clinical data management, including 2 years in medical coding with MedDRA and WHODrug., Proficiency in medical coding tools such as Medidata Coder or Central Coding., Fluent in English, both written and verbal..

Key responsibilities:

  • Perform clinical medical data coding independently on global projects.
  • Collaborate with project team members to ensure data quality and consistency.
  • Assist in developing and reviewing coding standards and project-specific conventions.
  • Support process improvements and maintain technical competencies.

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Fortrea XLarge https://fortrea.com/
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Job description

Job Overview:

Assisting with the data management leadership on a large global project, or multiple projects with responsibility for the Thesaurus Management; and technical oversight of all dictionary coding activities for the delivery of medical coded data according to Fortreaclient quality and integrity specifications, and project timelines and budgets. Develop and maintain a close liaison with project Lead Data Reviewer, core team members, and Clinical Lead Data Managers as appropriate.

      Summary of Responsibilities:

      • Perform the clinical medical data coding aspects of assigned projects on a global basis independently.
      • Work with the Manager and aide in personal career development, interpersonal skills, and achievement of competency standards.
      • Assist with the identification and implementation of solutions to project data management coding issues and concerns.
      • Serve as the project liaison including provision of project specific coding status.
      • Assist in review of Data management plan (wherever coding sections are applicable) andor
      • Study specific Dictionary Coding Conventions and Specifications.
      • Interact and collaborate with other project and specialty team members (clinical, programming, statistics, Clinical Data Management, drug safety, etc.) to support the setup, maintenance, and closure of the data management aspects of the project to ensure consistent, cohesive data handling and quality of coded clinical data.
      • Assist in development and implementation of global SOPs and Work Instructions within functional area; liaise with other disciplines in the development of SOPs that impact functional area.
      • Maintain coding technical competencies via participation in internal and external training seminars.
      • Support project staff on achieving client satisfaction (internal and external) through delivery of quality medical coded data, ontime, and onbudget.
      • Assist in identifying areas for process improvement, efficiency improvement and implement solutions on assigned projects.
      • Assist with the dictionary verification of Fortrea standard dictionaries and client dictionaries in a timely manner.
      • Perform dictionary verification on assigned projects.
      • Review literature and research technologiesprocedures for improving global thesaurus management practices.
      • All other duties as needed or assigned.
        • Qualifications (Minimum Required):

          • Universitycollege degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., professional registered nursing certification, medical or laboratory technology).
          • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
          • Fluent in English, both written and verbal.
            • Experience (Minimum Required):

              • Minimum three (34) years relevant work experience in clinical data management with 2 years clinical data coding experience (MedDRA and WHODrug).
              • Indepth knowledge of medical coding process and various coding tools (e.g., Medidata Coder, Central Coding, etc.).
              • Demonstrated interpersonal skills.
              • Excellent oral and written communication and presentation skills.
              • Indepth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
              • Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical biotechnological companies.
              • Broad knowledge of thesaurus management process.
              • Thorough knowledge of Standard Coding Dictionaries.
              • Knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs, especially as related to medical coding of clinical data.
              • Knowledge of effective clinical data management practices.
                • Preferred Qualifications Include:

                  • MedDRA Certified.
                  • Knowledge of Fortrea and the overall structure of the organization.
                  • Thorough knowledge of Fortrea standard operating procedures and work instructions.
                    • Physical DemandsWork Environment:

                      • Office or homebased work environment.
                      • Travel Requirements: Regional % Of time:5 % Of the above that requires overnight stay: 50 Travel is primarily to where: Varies

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Non-Verbal Communication
  • Social Skills
  • Teamwork
  • Problem Solving

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