Associate Director - Biostatistics Consultant, Remote - Inflammatory and Immune Diseases

February 4

Apply Now

Receive Emails with Similar Jobs

ClinChoice

WebsiteLinkedInAll Job Openings

ClinChoice is a global full-service contract research organization (CRO) established in 1995, specializing in clinical development, post-marketing, and functional service support for the pharmaceutical, biotechnology, and medical devices industries. They provide comprehensive solutions from early clinical development to post-approval lifecycle management, with expertise in a variety of therapeutic areas such as autoimmune and inflammation, dermatology, endocrinology, infectious diseases, neuroscience, and oncology. ClinChoice aims to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. The company supports its clients with clinical, regulatory, and operational expertise across all phases of product development.

Full-Service CRO • Clinical Development • Post-Marketing & Real-World Evidence • Quality and Compliance • Technology

1001 - 5000 employees

Founded 1998

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 Description

• Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? • ClinChoice is searching for a Associate Director/Director, Biostatistics to join one of our clients. • ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. • We are seeking an Associate Director/Director of Biostatistics. • Reporting to the VP of Biometrics. In this position you will be acting as the statistical lead for one or multiple studies, providing technical leadership and statistical support on the design, conduct and execution of the clinical studies. • You will partner closely with the cross-functional teams and provide expert biostatistic input on development plans, regulatory interactions, and study design. This may include but is not limited to authoring/review of statistics section in the protocol, sample size determination, authoring/review of statistical analysis plan and mock TFL, reviewing study randomization files, ADaM specs, CRF design, DMC charter, analyzing and interpreting the clinical study results, and ensuring statistical integrity. • Rich experience leading Integrated Summary of Safety, DSUR, IB would be preferred. • Key contributor on regulatory submissions and communication with global regulatory authorities. • Provide expert statistical advice, methodological research and analysis of trial and epidemiological data to inform the design, planning and execution of Client clinical studies. • Review and/or author statistical analysis sections of protocols, statistical analysis plans, clinical study reports, regulatory documents or scientific publications, generates or reviews study randomization, and sample size/power estimations. • Oversee and lead the vendor/CRO biostatistics teams, including activities during TFL development, Data Monitoring Safety Board meetings, interim analyses, and database locks. • Execute or oversee individual projects, which will include meeting with project/study team members, conducting exploratory analyses and graphic support, and providing analyses for publications of Client studies. • Evaluate alternative or innovative approaches to statistical methods and study design. • Build relationships with CROs and other external partners to achieve results for specific project needs. • Ensure the delivery of high quality and timely reports to project teams and clinical trial team.

🎯 Requirements

• PhD in statistics strongly preferred; Candidates with MS in statistics, biostatistics or mathematics and a depth of relevant experience in drug development statistical research will be considered. • A minimum of 10 years’ experience in progressive and relevant clinical trial experience. • Experience working in a matrix organization. • Ability to communicate and work directly with non-statisticians imparting and delivering complex statistical information to scientific development partners and researchers. • Excellent communication with an ability to present to a variety of stakeholders and tailor message accordingly. • Experience managing CROs and other data vendors. • Strong leader with a growth mindset, willing to learn from others, and dedicated to promoting a psychologically safe environment. • Ability to keep pace in a fast-moving organization and navigate ambiguity. • Advanced knowledge of statistical methods in clinical study designs (adaptive, Bayesian), statistical analysis methods including Bayesian method, missing data imputation, multiplicity adjustment. • Knowledge and proficiency in SAS or R and other industry computational tools. • Knowledge of CDISC standard including SDTM, ADaM. • Knowledge of ICH guidelines, FDA / EMA / other regulatory authority guidance. • Experience in planning, running and documenting simulations, including clinical trial simulations. • Experience working with in a remote virtual environment.