Senior Statistical Programmer – SR 412 views0 applications

Job Description

    Responsible for all programming aspects (analysis datasets, pooled datasets, listings and tables) of individual clinical trials as needed. Supervise CROs as required and ensure timely deliverables with highest quality. 1. Lead the programming activities for a trial or publication activities. 2. Maintain efficient interfaces with internal and external customers with support of CDS management, Program Programmer/ Statistician and CPOs as needed. 3. Develop resource plans as required with support of the Program Programmer. 4. Develop and comply with project / study standards and specifications following internal guidelines. 5. Make certain that documents and specifications are consistent and comply with company standards by providing input into CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities. 6. Program and deliver, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for clinical trials with high quality and within milestones. 7. In consultation with the statistician, develop specifications for analysis datasets, pooled datasets, and listings 8. As required, make certain that documents and specifications are consistent and comply with company standards for specifications of analysis datasets, pooled datasets, listings, summaries, figures and tables for clinical trials. 9. Support quality control and quality audit of deliverables. 10. Maintain records for all assigned projects and archiving of trial / project analysis and associated documentation 11. Participate in the selection of CROs and supervise the trial activities of the CROs as needed. 12. Provide input on process improvement initiatives and participate in non-clinical project activities with support from GH

Salary:Not Disclosed by Recruiter

Industry:Medical / Healthcare / Hospitals

Functional Area:Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology

Role Category:R&D

Role:Bio-Statistician

Desired Candidate Profile

Education-

UG:Any Graduate – Any Specialization

PG:Any Postgraduate – Any Specialization

Doctorate:Any Doctorate – Any Specialization, Doctorate Not Required

    University or college degree in life science, computer science, statistics or equivalent relevant degree. Fluent English (oral and written). 1. Intermediate knowledge of / experience with SAS software. 2. Working knowledge of database design/ structures. 3. Good understanding of global clinical trial practices, procedures, methodologies. 4. Good understanding of regulatory requirements relevant to SR (e.g. GCP, ICH). 5. Intermediate knowledge of office tools. 6. 3 – 5 years experience in a programming role preferably supporting clinical trials/ or in the pharmaceutical industry

 

Leave your thought

Share this job
We are a Staffing and Software Development company and a community of passionate, purpose-led individuals. We think disruptively to deliver technology to address our clients' toughest challenges, all while seeking to revolutionize the IT industry and create positive social change. A&J Global Solutions share the same cultural characteristics and imperatives. We come to work as ourselves. We enjoy each other’s company. We value honesty and transparency. Appearances and backgrounds aren’t important to us; ideas and doing the right thing are.We abhor and reject discrimination and inequality and promote diversity in all its forms. We proudly, passionately and actively strive to make both A&J Global Solutions and our industry more reflective and inclusive of the society that we serve.We are focused on helping our industry improve,& believe in sharing what we learn.We do this by writing books,talking at conferences,& championing open source.Our Agile development tools help our clients continuously improve & deliver quality software.
Connect with us

This is a demo store for testing purposes — no orders shall be fulfilled.