Job Description

Job Title: Principal Biostatistician

Job Location: US – Remote

Job Overview:

Provides all biostatistical services to meet the requirements of all Caidya clients, including full-service, Global Clinical Analytics (GCA), and other type studies.

Job Duties and Responsibilities:

A Principal Biostatistician is expected to be a very successful Senior Biostatistician who establishes excellence in one or more areas providing some unique leadership to Caidya. Examples of areas of excellence include but are not limited to:

• Proven written and oral communications with regulatory agencies.
• Special expertise in more complex statistical analytical methods not well known to all biostatisticians.
• Established expertise in a medical therapeutic area.
• Established a long-term high-level relationship with a Caidya sponsor.
• Overall high-quality work and a strong reputation for statistical knowledge.
• Exhibited leadership and organizational skills to plan, supervise, implement, and monitor the statistical processes for multiple clinical trials.
• Demonstrated ability to adapt and adjust to changing priorities and deal with uncertainty and risks.
• May be given some supervisory responsibilities for junior staff or department areas.

Supervisory Responsibilities:

• No supervisory responsibilities.

Job Requirements:

Education

• PhD or Master’s in statistics or related area, or equivalent degree globally

Experience

• PhD + 7-10 years (or MS + 10 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 junior staff members.
• Capabilities
• Excellent broad ranging understanding of statistical methods and issues. Demonstrates leadership in several areas of statistics.
• 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 performed routinely: Strong understanding of all departmental SOPs and good understanding of all required company SOPs.
• Familiarity with Caidya Functional Areas that Biostatistics interacts with on a regular basis (Proposals, Finance, Clinical Operations, Data Management, Medical Writing), and updates appropriate personnel regarding project scope changes which may impact their areas.
• Support the Business Development process through RFP process, bid defenses, attendance at scientific meetings, etc.

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