In addition to providing customers with statistical advice and carrying out the project primary role within a defined project team, the Senior Biostatistician works autonomously in the development and quality control of analytical plans, reports, derived datasets, tables, lists, and figures.
Responsibilities:
1 Operational Execution
Oversee and guide a project team to successfully complete a project on schedule and within budget.
Engage in crucial communication with clients regarding contractual and statistical matters.
Carry out quality control on derived datasets, tables, figures, and data listings created by department colleagues.
Continuously review one's own work to guarantee first-rate quality Recognize and use cutting-edge statistical techniques
Oversee the creation and quality assurance of analytical plans, statistical reports, integrated clinical report statistical sections, and other process-supporting documentation.
As an impartial statistician who does not cast a vote and provides statistics and analysis for the DMC review, play a supporting role.
Travel to, participate in, and attend all client meetings as needed (e.g., talking about analysis principles, presenting, debating, and interpreting study results)
2 Business Development
Supporting business development can take many forms, such as actively participating in internal and client meetings to discuss study design issues, offering and discussing sample size scenarios, assisting with budget and proposal development, and attending and preparing for bid defense meetings for prospective studies, work programs, and FSPs.
3 General Activities
Additional responsibilities as defined by supervisor/manager.
Requirements :
PhD in Statistics or related discipline with some experience or MS in Statistics or related discipline with significant experience
The knowledge of pharmacokinetic data is an advantage
Competent in written and oral English in addition to local language
Note : if you find any difficulties, please share your resume and also ,would like to refer any of your friends,
you may contact at : subramanyam.katperi@parexel.com
One of the biggest clinical research organizations (CROs) in the world, Parexel offers the whole spectrum of Phase I to IV clinical development services to expedite the delivery of life-saving medications to patients. Our team of more than 21,000 global professionals uses the depth of our clinical, regulatory, and therapeutic expertise to design and conduct clinical trials with patients in mind. By increasing access and participation, we can make clinical research a care option for anyone, anywhere. We collaborate with leading biopharmaceutical companies, up-and-coming innovators, and sites.
Our extensive industry experience and solid performance over the previous 40 years have advanced clinical research in the most challenging areas of healthcare, and our innovation ecosystem provides high-caliber solutions to improve efficiency at every stage of the clinical trial process. Every trial matters because of our exceptional staff, astute observations, and unwavering commitment to operational excellence, which enable us to strive every day to treat patients with dignity and perpetually learn from their experiences.
With Parexel being named "Best Contract Research Organization" by an independent panel for Citeline in November 2023, "Top CRO to Work With" by investigative sites worldwide in the 2023 WCG CenterWatch Global Site Relationship Benchmark Survey, and the recipient of the 2023 Society for Clinical Research Sites (SCRS) Eagle Award for advancing the clinical research profession through strong site partnerships, we continue to receive industry recognition for our approach.