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Anna Tayebnejad

@annatayebnejad

Statistical Analyst III at Medpace, developing SAS programs and statistical analyses for clinical studies.

At Medpace, I contribute to clinical development plans and review study protocols to identify appropriate statistical methodologies. I program study analyses, interpret results, and prepare statistical methods sections for clinical and statistical reports.

I develop ADaM, SDTM, and TFL programs and create macros to simplify programming processes. I also apply statistical models to safety and efficacy endpoints and work within CDISC and FDA standards.

Before Medpace, I coordinated cancer research trials at University of Colorado Anschutz Medical Campus, including patient consent, study data, and regulatory documentation. My work has also included data analysis and evaluation at Arapahoe County Early Childhood Council, and I’m a co-author on biomedical publications.

Experience

Work history, roles, and key accomplishments

Current

Statistical Analyst III

Current

Medpace

May 2022 - Present (4 years 5 months)

Contributes to clinical development plans, reviews protocols, and develops statistical methodologies for studies. Leads statistical programming teams and ensures compliance with CDISC and FDA standards.

SAS Adams SDTM TFLs CDISC FDA Pinnacle 21 Statistical Modeling Clinical Trials Quality Control Mentorship

Data Analyst, Program Evaluator Intern

Arapahoe County Early Childhood Council

Jul 2021 - Dec 2021 (5 months)

Provided data analysis and evaluation support using Excel, created statistical summary reports, and implemented database and survey designs. Produced and revised logic models for programs.

Excel Data Analysis Survey Design Theories Of Change Reporting

Clinical Research Coordinator

University of Colorado Anschutz Medical Campus

Oct 2018 - Jun 2021 (2 years 8 months)

Coordinated cancer research clinical trials, secured patient consent, and managed data collection. Ensured compliance with GCP, ICH guidelines, and HIPAA while maintaining regulatory documents and IRB communication.

Clinical Trials GCP ICH Guidelines HIPAA Electronic Data Capture Regulatory Compliance IRB Patient Consent Processing Data Management

Molecular Laboratory Technician

DNA Connexions

Apr 2017 - Mar 2018 (11 months)

Conducted DNA testing and genetic analysis, managed patient samples, and performed quality control. Performed PCR testing and gel electrophoresis.

DNA Testing PCR Gel Electrophoresis Quality Control Genetic Analysis

Clinical Research Assistant

Thomas J Stephens and Associates

Oct 2015 - May 2017 (1 year 7 months)

Managed clinical testing for medical topicals and devices, recruited study participants, and ensured IRB compliance. Calibrated equipment and organized study reports for sponsors.

Clinical Research IRB Compliance Patient Recruitment Data Collection Equipment Calibration Report Writing