Job Description

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 clinical medical data coding aspects of assigned projects with supervision.
• Work with Management and aid in personal career development, interpersonal skills, and achievement of competency standards.
• Collaborate with the Coding team and Lead Data Reviewer on all coding aspects for project(s) assignments including start-up, maintenance, and completion activities.
• Assist the project liaison including provision of project-specific coding status.
• Assist with implementing solutions to project data management coding issues and concerns.
• Assist in review of Data management plan (wherever coding sections are applicable) and/or Study-specific Dictionary Coding Conventions and Specifications.
• Support the 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.
• Achieve client satisfaction through delivery of quality medical coded data, on-time and on budget.
• Maintain Medical Coding competencies via participation in internal and external training seminars.
• Support globally based project staff on achieving client satisfaction (internal and external) through delivery of quality medical coded data, on-time and on-budget.
• Bring forward solutions for process and efficiency improvement on assigned projects.
• Assist with the dictionary verification on assigned projects.
• 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 verbal.



Experience (Minimum Required):• Minimum 3+ years of relevant work experience in data management.
• Excellent oral and written communication and presentation skills.
• Basic knowledge of the medical coding process and various coding tools (e.g., Medidata Coder, Central Coding, etc.).
• Knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
• 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. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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