Fortrea Virtual Hiring Event for SAS Professionals: Transforming Clinical Development with Innovation

Elevate your career with Fortrea, a leading global contract research organization (CRO) that’s passionate about scientific rigor and boasts decades of clinical development expertise. We’re hosting a Virtual Hiring Event for SAS Professionals on December 9th, offering exciting opportunities to join our dynamic team. Fortrea, formerly Labcorp Clinical Development and Commercialization Services, is revolutionizing drug and device development. Be part of our journey to shape the future of healthcare!

About the Company:

Fortrea Inc.: As a CRO with a global footprint and a commitment to scientific excellence, Fortrea provides a diverse range of clinical development, patient access, and technology solutions across 20+ therapeutic areas. With operations in 90+ countries and a team of over 19,000 professionals, Fortrea is at the forefront of transforming drug and device development.

Company Vacancies List:

Position Title: Statistical Programmer

No. of Posts: Multiple
Experience: 3-8 years in SDTM, ADAM, and TLFs
Location: Bangalore, Pune, Mumbai (India)
Time Type: Full time

Company Name: Fortrea Inc.

Company Address: Bangalore, Pune, Mumbai (India)

Fortrea Virtual Hiring Event for SAS Professionals

Detailed Job Description:

Role:

Develop and review SAS specifications, programs, and output for the creation of ADaM and client-defined analysis datasets, tables, listings, and graphs.
Interact with project team members in related disciplines, including Clinical Data Management, Clinical Operations, and Biostatistics.
Assume responsibilities as a team member, representing Statistical Programming at internal project team meetings and client meetings.
Demonstrate problem-solving skills, proactive decision-making, and the ability to seek advice from senior Statistical Programming staff.
With experience, assume the role of a Lead Programmer for assigned projects.
Assist in the training and mentoring of statistical programmers under the supervision of senior staff.

Responsibilities:

Prioritize personal workload to meet specified completion dates.
Conduct statistical programming reviews of case report forms, annotated CRFs, database structure, and study-related documentation.
Ensure quality and consistency in draft and final production runs for projects.
Maintain the filing of study documentation to the standard requirements according to processes and acceptable for audit.
Perform other duties as assigned by Senior Statistical Programming staff.

Experience:

3 to 5 years of experience as a Statistical Programmer for the management and reporting of clinical trial data.
Demonstrated skills in the use of SAS.
Effective time management skills and the ability to work to tight deadlines while maintaining the highest standards of work.
Awareness and appreciation of the business needs of a CRO.
Effective communication skills and a cooperative, team-oriented approach.