Senior Biostatistician

Everest Clinical Research Services Inc; Rickmansworth; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading clinical research organization, Everest Clinical Research, is looking for Senior Biostatisticians to join their growing team. This remote role requires expertise in statistical planning and analysis, ensuring timely project delivery while maintaining high-quality standards. Candidates should possess a Ph.D. or Master's in statistical science, along with relevant industry experience.

Qualifications

• Ph.D. with 2+ years relevant experience or Master's with 4+ years experience.
• Demonstrated ability and performance in statistical methodologies.

Responsibilities

• Lead resolution of daily issues and ensure project delivery.
• Design, analyze, and report on clinical trials and manage statistical programming.

Skills

Leadership

Statistical Analysis

Project Management

Data Management

Quality Control

Education

Ph.D. in statistical science

Master's degree in statistical science or related field

Job description

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Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to pharmaceutical, biotechnology, and medical device industries worldwide. We serve leading companies and work with advanced drugs, biologics, and medical devices.

Founded in 2004, Everest has a strong foundation as a statistical and data management center of excellence. Our headquarters are in Markham, Ontario, Canada, with additional sites in the USA, China, and Taiwan.

Known for quality, customer service, and flexibility, Everest is a dynamic, growing organization.

We are seeking dedicated, skilled, and customer-focused individuals to join our team as Senior Biostatisticians working remotely from the UK, in accordance with our Work from Home policy.

Key Responsibilities:

1. Leadership and Project Management: Lead resolution of daily issues, ensure quality, improve efficiency, and deliver projects on time to build client trust.
2. Statistical Planning and Methodologies: Design, analyze, and report on clinical trials; contribute to protocol writing; perform sample size calculations; develop randomization specifications; write SAPs; maintain QC and QA plans; assist with data management plans; develop statistical methodologies.

Statistical Programming:

1. Develop/review ADaM and SDTM dataset specifications; perform QC validation; lead statistical dry runs; review analysis documentation.

Analysis, Reporting, and Publication:

1. Perform analyses per SAP; validate results; contribute to reporting and dissemination; review CSR; write statistical reports; support publication efforts.

Data Collection and Cleaning Support:

1. Provide input on CRF design; review data management plans; program quality checks; assess data quality issues; assist with database lock preparations.

Additional Requirements:

• Complete required training; adhere to policies and SOPs; archive study files properly; pursue professional development activities.

Qualifications:

Ph.D. in statistical science or related field with 2+ years relevant experience, or Master’s with 4+ years relevant experience, demonstrating ability and performance.