Jobs at Syneos Health

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

The Single Sponsor Payment Specialist will assist in site management activities, maintain clinical tracking information, and coordinate supplies for assigned studies, ensuring compliance with protocols and guidelines.

Manage clinical trial sites, ensure compliance with regulations, assess site performance, conduct monitoring visits, and optimize site activities throughout the trial lifecycle.

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

The Principal Biostatistician leads biomarker-related statistical activities in clinical studies, develops evaluation plans, and performs complex data analysis, focusing on genomics and biomarkers.

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

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 CRA II conducts site qualification, monitoring, and management activities ensuring compliance with regulatory standards and protocols, while communicating with site staff and managing study progress.

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

The role involves managing clinical research projects, ensuring compliance with regulations, coordinating teams, overseeing budgets, and developing client relationships, while providing leadership and training to staff.

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

The role involves applying quality management expertise in a clinical setting, working collaboratively in a team to ensure effective drug development solutions.

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 managing project files, ensuring compliance with guidelines, providing administrative support, maintaining communication among team members, and assisting in quality assurance activities.

The role involves site management in clinical trials, including site qualification, monitoring, compliance verification, data accuracy, and communication with site staff to ensure regulatory standards are met.

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 site qualification, management activities, and ensuring compliance with regulations and protocols for clinical studies.

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.