Senior Biostatistician I

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Job Description: Job Title: Senior Biostatistician I Job Location: India (Remote) Job Overview: Provides biostatistical services to meet the requirements of all Caidya’ s clients, including full-service, Global Clinical Analytics (GCA), and other type studies. This may include but it’s not limited to: development and approval of Statistical Analysis Plans and table shells, randomization schemes, review of data management documentation, lead development of Protocols and approve the statistical section in Clinical Study Reports, serve as Quality Control Biostatistician or IDMC statistician. Job Duties and Responsibilities: Meets all the job duties, responsibilities, and requirements of a Biostatistician in addition to those listed here. Coordinate and approve Statistical Analysis Plans (SAP), mock-up tables, programming and derived dataset specifications developed by Biostatistics and Statistical Programming staff. Lead protocol development work including experimental design, randomization, sample size calculation, statistical methods, defining study objectives and parameters. Coordinate and approve the statistical section of the Clinical Study Report (CSR) written by Biostatistics staff and collaborate with Medical Writer in preparing the integrated CSR as needed. Coordinate and approve TFL and derived datasets, programming of derived datasets and Tables, Figures and Listings (TFL), and data review and statistical analysis developed by Biostatistics and Statistical Programming staff. Provide management of other Biostatistics Department requirements and functions, such as SOP updates, as requested by line manager. Serve as Quality Control Biostatistician for sample size calculation reports. Serve as IDMC / DSMB statistician as needed. Other duties commensurate with the position as assigned by line manager. Provide staff training and study oversight as requested by line manager. Provide staff oversight as mutually agreed with line manager. Supervisory Responsibilities No supervisory responsibilities. Job Requirements: Education PhD or Master’s in statistics or related area, or equivalent degree globally Experience PhD + 3-5 years (or MS + 5-7 years) experience in pharmaceutical, CRO, or related environment. Skills/Competencies Interpersonal and communication skills: Excellent written and oral communication skills including technical writing of all statistical results. Ability to develop professional presentations for presenting statistical issues and solutions to clients internally. Ability to effectively learn and handle new or unfamiliar statistical methods. Ability to find needed written resources and interact with other Biostat staff with the needed familiarity. Willingness to share expertise with younger staff members. Capabilities Excellent broad ranging understanding of statistical methods and issues. Has a developed expertise in 1-2 therapeutic areas. Ensures statistical quality: Reviews and monitors quality of statistical tasks and project deliverables provided by statistical project team. Deep working knowledge of clinical drug development process: In-depth understanding of phases of clinical trials and relevant statistical considerations that apply to Phase I-IV studies and non-inferiority concepts. Has strong knowledge of GCP and ICH guidelines and other regulatory guidelines related to statistics. Develops capability for interacting with regulatory agencies on behalf of sponsor matters. Such capability would include ability to write statistical reports and/or present oral arguments to such agencies. Ability to serve as a Project Manager for GCA studies. Coordinate keeping tasks and project activities in line with agreed timelines and budget. Excellent training and presentation skills: Has the ability to clearly communicate statistical concepts and successfully train and develop staff through coaching and presentations. Strong understanding of departmental and company procedures which relate to tasks that are performe

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