Jobs at Syneos Health

Lead RWD analysis strategy and execution: develop technical specifications and statistical programs, perform complex observational analyses (propensity scoring, ML), validate cohorts/variables, ensure QC, collaborate cross-functionally, and communicate results to non-technical stakeholders.

The Clinical Scientist collaborates with Medical Directors to develop medical plans, reviews data for trends, manages project scopes, and ensures adherence to clinical protocols while participating in audits and meetings to improve study integrity.

The Clinical Scientist supports medical plan development, data analysis, and medical reviews while ensuring compliance with guidelines and project milestones.

The Clinical Scientist in Oncology collaborates with Medical Directors to develop medical plans, perform data reviews, author queries, and manage project scope and quality, ensuring adherence to guidelines and timely project delivery.

The Director of Epidemiology Pipeline collaborates on virology clinical trials, providing scientific expertise, leading project proposals, and overseeing study management and regulatory compliance.

Lead global Phase 2b clinical studies in inflammation, oversee project execution, manage timelines and budgets, and mentor project teams.

The Clinical Data Reviewer is responsible for clinical data assessment, checking data validity, generating queries, and supporting clinical trials for oncology drug development, ensuring data quality for submissions and analyses.

The Senior Clinical Project Manager will lead Phase III oncology and hematology trials, managing projects and cross-functional teams while ensuring timely and quality delivery.

Manage and deliver operational and financial aspects of clinical projects, ensuring compliance with GCP, project timelines, and budget management while overseeing project teams.

The Internal Account Director will lead patient recruitment and retention strategies for clinical trials, ensuring successful enrollment and collaboration with various stakeholders.

The Principal Biostatistician leads biomarker analysis for clinical studies, develops evaluation plans, conducts data analyses, mentors staff, and ensures accurate statistical deliverables while collaborating across teams.

The Sr CRA performs site qualifications, initiates and manages sites according to GCP, ensures compliance, supports recruitment, and mentors junior staff.

The role involves programming and data review for real-world data analysis, supporting epidemiologists, and managing complex data sets using statistical programming languages and tools.

Responsible for monitoring clinical trial sites, ensuring compliance with regulatory standards, managing site activities, and supporting patient recruitment throughout study lifecycle.