Senior Biostatistician

Serves as lead biostatistician on clinical studies. Maintains the statistical integrity of clinical trials analyzed by SDC. Actively participates in writing statistical sections of protocols, preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, writing statistical sections of clinical study reports, and participating in meetings with drug regulatory agencies as required.

Primary Responsibilities

• Act as the lead statistician on clinical research projects
• Provide statistical expertise for study design of clinical trial protocols
• Write statistical methods section of the study protocol, as needed
• Write statistical analysis plans ensuring appropriate regulatory requirements and study objectives defined in the study protocol are followed
• Review CRFs to ensure consistency with protocol and adequacy in collecting data to meet objectives and statistical analyses defined in the protocol
• Program summary tables, data listings and graphical representations of clinical trials data
• Ensure proper execution of all analyses defined in the statistical analysis plan as well as any post-hoc analyses and relevant exploratory analyses of clinical trial data
• Prepare key sections of clinical study reports and various regulatory documents
• Perform statistical QC of final clinical study reports
• Provide statistical support to answer questions from external clients (such as FDA, Investigators)
• Contribute to the development of standard operating procedures for clinical trials
• Represent statistical operations department at regulatory meetings, sponsor meetings, and any other multifunctional meetings, as needed
• Manage biostatistics timelines, budgets, and client expectations
• Adhere to all aspects of the SDC’s quality system
• Comply with SDC’s data integrity & business ethics requirements
• Perform other related duties incidental to the work described herein
• Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements

Requirements

• Excellent analytical skills, with the ability to process scientific and medical data
• Able to work independently
• Excellent knowledge of statistical programming
• Expertise in manipulating and analyzing SAS data
• Ability to identify data issues, present problems, and implement solutions.
• Capability of communicating technical concepts clearly, concisely, and understandably to non-statistical colleagues
• Good leadership, organizational and time management skills, with the ability to multi-task
• Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP)
• Strong interpersonal communication and presentation skills
• Ability to effectively collaborate across cross-functional teams
• Focus on quality at all times and in all situations

Benefits

What you can expect from us:

• Competitive wages
• Flexible work schedules
• Fully remote roles
• Variety of therapeutic areas
• Career advancements
• Medical insurance
• HSA with company match
• Dental with 2 coverage options
• Vision
• 401K with company match
• Paid Time off
• Over 10 company holidays
• Life Insurance
• Inclusive and collaborative company culture
• Identity theft protection
• Voluntary accident and critical illness insurance