
51 - 200 employees
💼 Consulting
🏥 Healthcare
🧬 Biotechnology
Consulting • Healthcare • Biotechnology
Clinical Outcomes Solutions is a global clinical outcomes consultancy that provides comprehensive support and services in all aspects of Clinical Outcome Assessment (COA) research. The company helps inform patient care by capturing the patient voice through innovative scientific methods. It guides organizations in navigating the complexities of clinical outcomes research by crafting strategies and solutions to capture accurate data. Trusted by pharmaceutical and biotechnology companies, the firm ensures regulatory compliance and optimized patient outcomes.
📡 We watch Clinical Outcomes Solutions's careers page
Several times a day
how often we check
13
roles posted in the last 30 days
About 34 days
usual time to fill a role
174
roles closed in the last year
Selected: 🆕 Date Added.
🕒 5 days ago
Senior Clinical Data Manager ensuring accurate, compliant clinical trial data for pharmaceutical studies. Managing data reviews, discrepancies, database locks, and clinical system access.
🕒 October 30
Vice President leading Cytel’s India-based FSP operations for pharmaceutical and biotechnology clients. Driving operational excellence, client delivery, workforce strategy, financial performance, and business growth.
🕒 October 28
Associate Director leading biostatistical strategy and analysis for Cytel’s sponsor-dedicated pharmaceutical clinical trials. Supporting Phase II–III drug development from protocol design through regulatory reporting.
🕒 October 28
Associate Director leading statistical strategy and trial delivery for Cytel’s sponsor-dedicated pharmaceutical programs. Supporting Phase II–III studies with SAS/R, regulatory submissions, and advanced analytics.
🕒 October 26
Senior Research Consultant leading systematic literature reviews and HTA-compliant evidence packages for Cytel’s biopharma analytics business. Managing clients, deliverables, junior researchers, and business development.
🕒 October 23
Remote Clinical Data Manager testing Medidata Rave EDC and clinical trial systems. Ensuring compliant, inspection-ready builds through scripts, regression testing, and defect resolution.
🕒 October 15
Senior Biostatistician supporting Cytel’s pharmaceutical clients with clinical trial design, analyses, and regulatory submissions. Developing SAPs, ADaM specifications, and clinical study reports.
🕒 October 15
Senior Biostatistician supporting Phase I-IV clinical trials for Cytel’s pharmaceutical clients. Delivering statistical analyses, regulatory submissions, SAPs, and clinical study reports.
🕒 October 14
Principal Statistical Programmer delivering SAS and CDISC programming for pharmaceutical clinical trials. Supporting regulatory submissions, CRO oversight, and high-quality clinical reporting.
🕒 October 8
Senior NONMEM Programmer generating PK/PD analysis datasets and e-submission packages for Cytel’s pharmaceutical clients. Supporting clinical modeling teams with R, SAS, QC, and data processes.
🕒 October 7
Senior NONMEM Programmer generating PK/PD datasets and e-submission packages for pharmaceutical clients. Using R and SAS to support clinical development and modeling activities.
🕒 October 2
Remote Senior/Principal Statistical Programmer supporting pharmaceutical clinical trials with SAS and R. Producing CDISC datasets, analyses, regulatory submissions, and overseeing CRO programming deliverables.
🕒 September 28
Senior Statistical Programmer using SAS and CDISC standards for a global pharmaceutical client. Supporting clinical-trial data analysis, validation, reporting, and submissions.
🕒 September 25
Senior Biostatistician supporting Phase I-IV clinical trials and regulatory submissions for Cytel’s pharmaceutical clients. Developing SAPs, analyzing data, and preparing integrated clinical study reports.
🕒 September 24
Senior Statistical Programmer using SAS and CDISC standards for Cytel’s pharmaceutical client. Supporting Phase I-IV clinical trials through data analysis, validation, and regulatory submissions.
🕒 September 24
Senior Clinical Data Manager overseeing clinical trial data management, CRO delivery, and regulatory readiness for a pharmaceutical client. Leading EDC, timelines, budgets, audits, and data quality.
🕒 September 24
Principal Statistical Programmer delivering SAS and CDISC clinical-trial reporting for Cytel’s pharmaceutical client. Overseeing CRO programming and supporting regulatory submissions.
🕒 September 17
Principal Data Scientist integrating biomedical signals, clinical data, and machine learning. Supporting Cytel’s pharmaceutical clients with scalable pipelines and reproducible health research insights.
🕒 September 16
Senior Statistical Programmer using SAS and CDISC standards for a pharmaceutical client. Supporting clinical-trial data analysis, submissions, validation, and global study teams.
🕒 August 21
Senior Statistical Programmer using SAS and CDISC standards for Cytel’s pharmaceutical client. Supporting Phase I-IV clinical trials through analysis, validation, and submissions.
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