Indegene walk-in for Junior Analyst
Company :
Indegene
Website :
Job Role :
Junior Analyst - Biostatistics
Eligibility :
MS/MSc
Experience :
1 - 6 Years
Job Location :
Bangalore
Walk-In Date :
28 Dec 2019
Walk-In Time :
10:00 AM - 01:00 PM

Company Profile:

We offer scientific partnership to global life science companies by delivering a spectrum of medical, marketing, training, intelligence, and analytics services.
The depth of our scientific expertise, scale of operations, offshore delivery model, global footprint, and intellectual property (IP) help us deliver value across multiple dimensions. We offer cost-effective solutions and services. We have the ability to work with global teams and their local affiliates for marketing and educational programs.
Our IPs have helped global clients in developing innovative platforms and solutions for various research and development programs.

Job Description:

The Biostatistician will be responsible for delivering statistical analytic solutions for Medical Affairs studies (MA), Non-Interventional studies (NIS), Scientific Analytics studies and multiple Phase I-IV clinical trials at a trial level by executing statistical analyses plans, ensuring high quality and timely production of statistical reporting deliverables (analysis datasets, tables, listings and graphs).
Responsible and accountable for the statistical activities and support on statistical solutions for trials/publications and conferences.
Activities include providing input on statistical scientific and operational aspects of the planning, design and reporting of trials/experiments, and production and delivery of statistical deliverables and exploratory analyses.
Responsible for transcribing analysis plans into computational solutions for the statistical programmer to implement (specifications of derived variables, specification and development of statistical computing solutions for inferential statistical analyses, tables and listings templates for key reporting documents like the CSR) of Phase I-IV clinical trials.
Ensure that documents, specifications, programs/macros 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.
Assume responsibility for reporting and analysis execution for multiple studies.
Responsibilities include, leading statistical deliverable meetings with necessary clinical trial team members and third parties, and exploratory analyses for ad-hoc analyses.
Expected to provide support for publications for individual clinical trials, and scientific analytical solutions.
Lead study teams to ensure high quality for all assigned deliverables and processes and ensure audit-readiness.
Responsible for ensuring statistical deliverables are provided to agreed timelines.
Maintain and build effective relationships with internal and external customers, utilizing support of management as needed.
Take lead role to collaborate with other line functions including the clinical trial team.
Explain statistical concepts in a manner easily understood by non-statisticians, and provide adequate statistical justifications for actions/decisions/statements, when required.
Provide statistical analysis solutions when exploratory analyses are required. Implement novel methods and innovative trial designs with support from lead statistician and/or statistical methodology as required.
Develop and comply with project / study standards and specifications following internal guidelines.
Support quality control and quality audit of deliverables.
Provide input on process improvement initiatives and participate in non-clinical project activities with support from group head.
Participate in non-clinical project activities as needed.
Provide support, coaching and mentoring to more junior statisticians.
Effective participation and contributions in the Clinical Trial Team and CDS project team.
Effectiveness of communication and team behaviors as assessed by the other members of the Clinical Trial Team and CTS project team.
Contribution to the exploratory analyses as and when required.

Skills:

Working knowledge of/experience with R or any other business or research analytic software with an expertise in at least one type of software.
Statistical and numerical knowledge and expertise in analytic aspects.
Excellent interpersonal and communication skills.
Strong understanding of global clinical trial practices, procedures, methodologies.
Strong understanding of regulatory requirements for design, analysis and reporting of clinical trials.

Venue Details:

Indegene Pvt Ltd,
Aspen G-4 Block, Manyata Embassy BusinessPark,
Nagavara, Bengaluru - 560045.

Contact Details:

Sirisha
080-4674-4567