Exciting opportunity to be part of the Fortrea India Apprentice Program!
As a Fortrea Apprentice, you will have the opportunity to support meaningful assignments that compliment an education in STEM+ Business and Healthcare disciplines, and are inspiring and valuable in our mission to improve health and improve lives across the globe
Capitalize on a dedicated training and development program that will support your scientific and professional career aspirations and take pride in delivering work that helps save the lives of millions of people around the world.
Education/Qualifications/Skills:
BE/ B Tech. (ECE, CSE, ISE, Electrical), MCA, M.Sc in Statistics.
Technical/Functional Knowledge on Statistics / Clinical domain knowledge would be added advantage along with excellent Programming skills is a must.
Good knowledge on SQL and UNIX environment.
We are looking for young and enthusiastic programmers who can be part of our Dynamic team.
Knowledge of SAS, R programming, and Python experience will be an added advantage
About Team:
Biometrics Team performs all the tasks which includes Statistical Analysis and Programming. we have 700+ Statistical Programmers with an average of 10 years of drug, device, or biologics development expertise. We have been providing quality statistical services to clients for more than 30 years. Our globally harmonized SAS environment and processes ensures 24/7 continuity and resourcing models to offer efficiencies across diverse portfolio.
Our Team delivers customized global solutions that enable you to manage your clinical operations and clinical trials with greater efficiency and flexibility. We deliver quality people, intelligent process, and deep technical expertise with an emphasis on performance measurement and accountability.
Apprenticeship Summary:
The Apprentice participates in and executes the entry level department functions (Designation of Apprentice) in accordance with Fortrea and/or sponsor Standard Operating Procedures (SOPs)
Analyzing and Programming of Clinical Trials data.
The project scope is to understand the drug development process; it's evolution into modern day methods of drug design. This gives the insight on the various components like the clinical trial protocol, informed consent form, case report form, and all regulatory submissions for IND application and NDA applications.
It also helps candidates in getting a good knowledge on the clinical data understanding, organizing, analyzing, and finalizing reports for efficacy and safety for the new development product.