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.

• Develop and review SAS specifications, programs and output for the creation of ADaM and client-defined analysis datasets, tables, listings and graphs in support of Statistical Analysis Plans
• Interact with project team members in related disciplines e.g. Clinical Data Management, Clinical and Biostatistics.
• Assume team member responsibilities, including representing Statistical Programming at internal project team meetings and with support from senior Statistical Programming staff at client meetings.
• Demonstrate good problem solving skills, a proactive approach and a willingness to make decisions, seeking advice from senior Statistical Programming staff to confirm decisions when necessary.
• With sufficient experience assume the role of a Lead Programmer for assigned projects.
• Understand scope of project in order to advise Senior Statistical Programming staff of changes in scope of projects to enable the timely development of change orders.
• Assist with training, mentoring of Statistical Programmers under the supervision of senior Statistical Programming staff.

• Participate in the Statistical Programming review of Case Report Forms(CRFs), annotated CRFs, database structures and study related documentation

• Review draft and final production runs for projects to ensure quality and consistency.
• Ensure the filing of study documentation is maintained to the standard required according to processes and acceptable for audit.
• Prioritize personal workload to meet specified completion dates.

• Carry out all activities according to Fortrea SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).

• Perform other duties as assigned by senior Statistical Programming staff.

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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