Senior Biostatistician – Complex Longitudinal Registry, Real-World Data

Posted Sep 2

This is a fully remote position, open to applicants in North Carolina.

📋 Description

• Act as the statistical lead on prominent client-facing initiatives

• Work collaboratively with cross-functional teams

• Design research studies

• Create statistical analysis plans

• Supervise analytical processes

• Offer strategic statistical guidance for the generation of high-quality, scientifically sound real-world evidence

• Assist with consulting tasks, pharmacovigilance, and registry management within the Real-World Science department


⛳️ Requirements

• A Master’s degree and/or a Doctorate degree in Biostatistics, Statistics, Bioinformatics, Mathematics, or a related quantitative discipline is required

• An equivalent combination of relevant education, training, and/or directly related experience may be deemed adequate

• At least 5–8 years of post-Master’s or 3–5 years of post-doctorate experience in applied statistical programming within a research, pharmaceutical, biotechnology, CRO, or medical environment is required

• Proven experience in leading complex observational research studies, such as longitudinal, EMR, or registry data, is necessary

• Experience with intricate longitudinal registry or real-world data is required

• In-depth knowledge of retrospective and prospective observational study designs and associated methodologies is essential

• Advanced proficiency in R is mandatory

• A solid understanding of statistical methodologies for observational and longitudinal data analyses is required

• Ability to independently manage projects, prioritize competing deadlines, and handle multiple timelines

• Strong scientific, analytical, problem-solving, leadership, and communication skills

• Capability to collaborate with cross-functional teams and convey complex statistical ideas to both technical and non-technical audiences

• Exceptional attention to detail and dedication to producing high-quality, reproducible analyses and documentation

• Excellent written communication skills and commitment to best practices in statistical programming and code documentation

• Ability to make independent decisions with minimal supervision

• Strong interpersonal skills and a team-oriented approach

• Must possess legal authorization to work in the US without sponsorship

• Must successfully pass a comprehensive background check, including a drug screening


🏝️ Benefits

• Fully remote work arrangement

• Reasonable accommodations available for individuals with disabilities

• Additional benefits and employment privileges

People also viewed

Abbott13 hours ago

Clinical Research Associate I

US flagCalifornia, +1 more stateFull-timeClinical Research$61.3k – $122.7k/year
ApplyView job
Amgen13 hours ago

Global Feasibility Manager

US flagUnited States OnlyFull-timeClinical Research$103.2k – $139.6k/year
ApplyView job
Abbott14 hours ago

Clinical Research Associate I

US flagIllinois OnlyFull-timeClinical Research$61.3k – $122.7k/year
ApplyView job
Tempus AI16 hours ago

Clinical Data Manager

US flagIllinois OnlyFull-timeClinical Research
ApplyView job
Bicara Therapeutics16 hours ago

Senior Clinical Trial Manager

US flagUnited States OnlyFull-timeClinical Research$179k – $206k/year
ApplyView job
Eli Lilly and Company17 hours ago

Director – Clinical Pharmacologist, Clinical Research Physician

US flagUnited States OnlyFull-timeClinical Research$201k – $393.8k/year
ApplyView job

Never miss a great job!

Get handpicked remote jobs straight to your inbox weekly.

Trusted by 7,400+ designers