Jobs at Syneos Health

Assist in governance meetings, draft minutes, proofread labeling documents, ensure compliance in labeling processes, and manage templates.

The Project Manager II coordinates clinical study timelines, collaborates with teams, ensures compliance with regulations, oversees operational aspects of trials, and develops recruitment strategies for successful enrollment.

Manage clinical trials by planning timelines, coordinating with teams, adapting strategies, ensuring protocol adherence, and monitoring site/vendor performance.

Manage and coordinate clinical research studies, ensuring compliance with regulations, maintaining study documentation, and facilitating communication among stakeholders.

Manage interdisciplinary clinical research studies, ensuring compliance with GCP and regulations, overseeing project delivery, and acting as a liaison with customers.

The CRA II/Senior CRA will perform site management activities, ensure compliance with regulations, conduct monitoring visits, and support recruitment efforts throughout the clinical trial process.

The Principal Biostatistician oversees statistical tasks, mentors staff, prepares analyses, and ensures high-quality deliverables throughout project lifecycle.

The Executive Assistant provides high-level administrative support to the Business Unit Head, managing calendars, travel, communications, and preparing executive presentations. Skills needed include organization, discretion, and strong communication.

Ensure effective clinical research operations, monitor study progress, adhere to regulations, and coordinate communication with clinical trial participants.

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.

Conduct on-site and remote monitoring of clinical research studies, oversee junior staff, ensure compliance with protocols, and collaborate on trial activities.

Lead digital recruitment strategies for clinical trials. Provide strategic counsel to sponsors, oversee digital recruitment channels, and track performance using data insights.

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

The Associate Director of Epidemiology RWE provides operational and technical support for RWE studies, ensuring timely task execution and documentation accuracy.

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 role involves site management, including monitoring, qualification, and ensuring compliance with regulations while collaborating with clinical teams and site personnel. Responsibilities also include managing data integrity and documenting site activities.