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Associate Coding Specialist
2 months ago
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Perform the clinical medical data coding aspects of assigned projects with supervision. Work with the technical service group staff and aide in personal career development, interpersonal skills, and achievement of competency standards Assist the technical leader on all coding aspects for project(s) including start-up, maintenance, and completion activities. Assist in review of Data management plan (wherever coding sections are applicable) and/or Study specific Dictionary Coding Conventions and Specifications with supervision of senior dictionary coding specialist. Learning and understanding set-up, maintenance, and closure of the data management aspects of the project to ensure consistent, cohesive data handling and quality of coded clinical data. Learning and understanding the development and implementation of global SOPs and Work Instructions within functional area. Achieve client satisfaction through delivery of medical coded data, on-time and on budget. Maintain technical competencies via participation in internal and external training seminars. Support locally based project staff on achieving client satisfaction (internal and external) through delivery of quality medical coded data, on-time and on budget. Give inputs or solutions for process and efficiency improvement on assigned projects. Review literature and research technologies/procedures for improving global thesaurus management practices. Perform other duties as assigned by management. And all other duties as needed or assigned.Qualifications (Minimum Required):
University/college degree (life sciences, health sciences, information technology or related subjects) or a certification in allied health professions from an appropriate accredited institution. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Fluent in English, both written and verbalExperience (Minimum Required):
Minimum 2 to 4 years’ relevant work experience in data management. Excellent oral and written communication and presentation skills. Basic knowledge of medical coding process and various coding tools (e.g., Medidata Coder, Central Coding, etc.) Basic knowledge of clinical trial process and data management. Basic knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies. Demonstrated interpersonal skills.Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.