Jobs at ClinChoice

The Senior RWE Analyst Consultant will lead statistical analyses, mentor junior analysts, design solutions for RWE studies, and drive innovations in data analysis with client engagement.

The Clinical Data Manager will oversee clinical trial data management activities, ensuring data accuracy, integrity, and compliance with regulatory standards while coordinating with cross-functional teams.

The Senior Statistical Programmer Consultant will manage programming tasks for clinical trials, oversee deliverables, and validate datasets while ensuring compliance with industry standards.

The Senior Statistical Programmer Consultant supports clinical programming tasks, ensuring high quality deliverables, compliance with standards, and collaboration with the study team. Requires expertise in oncology and statistical programming.

Lead statistical activities for oncology clinical trials, providing strategic input, developing analysis plans, and mentoring junior statisticians. Collaborate on regulatory submissions and ensure compliance with standards.

The Clinical Supply Specialist manages clinical supply execution including planning, shipment oversight, inventory tracking, and coordination with stakeholders and vendors across EU and US.

Lead cross-functional teams to manage complex clinical trials across various health sectors while ensuring compliance with GCP and regulatory standards.

Lead and manage clinical projects, ensuring compliance with regulations and overseeing trial operations, specifically in hematology and oncology.

The Principal Statistical Programmer Consultant leads programming efforts for clinical studies, ensuring quality deliverables and compliance with industry standards, while collaborating with study teams and managing concurrent project activities.

The Principal Data Scientist Consultant will develop and maintain clinical datasets using R, ensure CDISC compliance, generate reports, and contribute to internal tools while collaborating with clinical teams.

The Senior Biostatistician will lead statistical strategy for clinical trials, oversee deliverables, ensure regulatory compliance, and support cross-functional teams.

The Senior Biostatistician will lead statistical strategy for clinical trials, provide statistical analyses, collaborate across teams, and ensure compliance with regulatory standards.

The Business Development Director is responsible for driving growth by securing new clients and expanding services, managing the full sales lifecycle, and maintaining relationships with key stakeholders in the life-sciences industry.

The Business Development Director will drive growth in pharmacovigilance and regulatory services by securing new clients and expanding existing accounts through full sales lifecycle management.

Seeking a Statistical Programmer II/III to develop and maintain statistical programs primarily using R and SAS for clinical trial data analysis, collaborating with clinical teams to ensure compliance and support submissions.

The Senior Statistical Programmer will program and validate datasets for clinical trials, oversee deliverables, manage projects, and ensure compliance with industry standards. Requires strong skills in SAS and R for statistical programming.