Worldwide Clinical Trials

Senior Statistician

DURHAM, NCPosted a month ago

Job summary

  • Job post source

    This job is directly from Worldwide Clinical Trials

  • Job overview

    The Senior Statistician role at Worldwide Clinical Trials involves independently managing statistical project support and providing expert consultancy to improve clinical trial outcomes and data analysis.

  • Responsibilities and impact

    The role includes managing statistical support for projects, reviewing study designs and analysis plans, assisting in clinical trial design, liaising with sponsors and internal teams, preparing reports and datasets, developing SAS programs, validating software, contributing to publications, supporting bidding processes, and improving data processing efficiency.

  • Compensation and benefits

    The salary ranges from $84,755 to $168,245 depending on skills, experience, and location; specific benefits are not detailed in the description.

  • Experience and skills

    Candidates must have a degree in mathematics, statistics, or a related field with strong statistical components, expert-level project statistician experience, design and analysis consultancy skills, and proficiency with statistical software like SAS and nQuery.

  • Career development

    Promotion depends on proven competency, responsibility level, and ability to work independently rather than just years of experience, indicating a merit-based growth environment.

  • Work environment and culture

    Worldwide Clinical Trials values diversity, inclusion, collaboration, creativity, and supports professionals to thrive by being themselves in a supportive and innovative environment.

  • Company information

    Worldwide Clinical Trials is a global midsize CRO with over 3,500 experts focused on innovative clinical research to find cures for persistent diseases, emphasizing quality and excellence.

  • Application process

    Applicants are encouraged to visit the company's careers page and LinkedIn for more information and other roles; specific application steps are not detailed.

  • Unique job features

    The job offers opportunities to lead system and process improvements, work with regulatory standards like ICH and FDA, and contribute to high-impact clinical research projects.

Company overview

Worldwide Clinical Trials is a global contract research organization (CRO) that provides phase I-IV clinical trial services to the pharmaceutical and biotechnology industries. They specialize in therapeutic areas such as neuroscience, cardiovascular, metabolic, and rare diseases. Founded in 1986, the company has grown to operate in more than 60 countries, leveraging their scientific expertise and innovative technologies to deliver high-quality data and support drug development. Their revenue is primarily generated through service contracts with pharmaceutical companies, offering comprehensive clinical trial management, data analysis, and regulatory support.

How to land this job

  • Position your resume to highlight your expertise in statistical project management, clinical trial design, and SAS programming, as these are core responsibilities for the Senior Statistician role at Worldwide Clinical Trials.

  • Emphasize your experience with statistical analysis plans, CDISC datasets (SDTM and ADaM), and regulatory knowledge including ICH and FDA guidelines to align with the job's technical and compliance requirements.

  • Apply through multiple platforms including Worldwide Clinical Trials’ corporate careers page and LinkedIn to maximize your application visibility and increase your chances of being noticed.

  • Connect with statisticians and biostatistics leaders at Worldwide Clinical Trials on LinkedIn, using ice breakers like commenting on recent clinical trial innovations or asking about their approach to statistical design and analysis improvements.

  • Optimize your resume for ATS by incorporating keywords such as 'statistical consultancy,' 'clinical trial design,' 'SAS programming,' 'CDISC,' 'ICH guidelines,' and 'FDA Quality System Regulation' to ensure it passes automated screenings.

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