Clinical Research Associate II conducting onsite monitoring and regulatory support for PSI, a contract research organization. Managing sites, CRF review, queries, and study progress across clinical trials.
About the role
- Biostatistician developing statistical analysis plans, SAS analyses, and reports for Celerion’s clinical research programs. Supporting randomization, data interpretation, and client deliverables.
Responsibilities
- Develop statistical analysis plans for simple to complex studies, including table shells and, when appropriate, other programming plans
- Direct and oversee execution of planned statistical analysis and summarization for simple to complex studies, including tables, figures, and data listings
- Perform data analysis and interpretation
- Provide input on data collection methods and coordinate customized electronic database transmissions to sponsors
- Support randomization by generating randomization schedules and plans
- Write statistical methods and results sections of assigned project reports
- Review draft reports for consistency and completeness
- Communicate with colleagues and clients regarding timelines, deliverables, and commitments
- Provide programming assistance as applicable
- Interact with internal departments including data management and project management
- Lead and/or participate in functions required for department and/or market segment team success
Requirements
- Master's degree in Statistics-related field and 3+ years industry experience or the equivalent OR Bachelor's degree in Statistics-related field and 3+ years industry related experience and 4+ years SAS programming experience or the equivalent
- Proficiency with SAS programming
- Ability to organize multiple priorities
- Excellent communication and leadership skills
- Demonstrated problem solving and decision making skills
- Excellent interpersonal skills
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
Report this job
Found something wrong with the page? Please let us know by submitting a report below.
Senior Clinical Research Associate conducting onsite monitoring and regulatory activities for a global medical research company. Supporting Phase II/III studies and Canadian clinical - trial sites.
Clinical Research Associate monitoring investigative sites and clinical trials for AbbVie’s innovative medicines pipeline. Ensuring patient safety, data integrity, compliance, and recruitment performance.
Clinical Research Associate monitoring Novo Nordisk clinical trials across Greater Montreal. Ensuring site compliance, patient safety, data integrity and timely study delivery.
Senior Clinical Scientist leading oncology clinical trials for ICON’s sponsor - dedicated research programs. Providing medical monitoring, scientific oversight, and protocol execution across US and Canadian locations.
Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organization. Ensuring protocol, ICH - GCP, and regulatory compliance across investigative sites.
Clinical Scientist interpreting WES/WGS data and classifying variants for SeqOne, a clinical genomics company. Supporting rare - disease diagnostics through regulated, patient - centered genomic reporting.
Clinical Research Associate monitoring clinical trial sites for Parexel, a global clinical research organization. Ensuring patient safety, data quality, regulatory compliance, and site delivery.
Clinical Research Associate monitoring clinical trials for ICON’s global healthcare research organization. Ensuring protocol, ICH - GCP, SOP, and regulatory compliance across investigative sites and remote work.
Senior Clinical Data Manager leading oncology clinical trials at Fortrea, a global clinical research organization. Owning data management from study start - up through database lock.