Jobs at Syneos Health

Performs on-site and remote site qualification, initiation, monitoring and close-out visits to ensure ICH-GCP/GPP and protocol compliance. Verifies informed consent, source data vs CRF, manages IP and ISF/TMF reconciliation, documents monitoring activities, supports recruitment and audit readiness, and collaborates with sponsors and site staff. May perform chart abstraction and train junior staff in real-world late-phase studies.

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.

The Regulatory Consultant will support global regulatory CMC for marketed small molecule products, preparing documentation and collaborating with cross-functional teams on submissions.

Senior data analyst/programmer using SAS or R to analyze commercial claims and EHR real-world data. Create longitudinal cohorts, derive baseline/outcome variables, assess data quality, apply epidemiologic study designs and statistical methods (regression, survival), review protocols/SAPs, and program TFLs. Familiarity with OMOP CDM and OHDSI tools is a plus; prior pharmaceutical experience preferred.

Lead statistical programmer developing SAS code and ADaM-specified datasets, tables, listings, and graphs for clinical trials. Ensures quality, validation, documentation, inspection readiness, mentors programmers, manages timelines, participates in sponsor meetings, and follows regulatory and SOP requirements.

Lead and deliver statistical activities across clinical trial lifecycle: prepare SAPs, generate randomization schedules, review CRFs and database design, coordinate biostatistics and programming teams, perform QC/verification, support regulatory interactions, mentor staff, and contribute to business development. Minimal travel.

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

Lead and deliver high-complexity pre-award feasibility assessments for global clinical trials across therapeutic areas. Independently analyze site-level data, prepare presentations/reports, support bid defenses, liaise with internal stakeholders, mentor junior staff, and contribute to process and data asset development to support RFPs and feasibility strategy.

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

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.

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

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.

The Principal Statistician oversees biostatistics projects, mentors staff, prepares statistical plans, and ensures quality and regulatory compliance in clinical trials.

The Manager of Biostatistics oversees biostatisticians, ensuring project quality, adherence to regulations, and managing staff development while meeting financial targets.

The Central Risk Manager provides expertise in developing monitoring strategies, assesses project risks, collaborates with teams, and ensures compliance with protocols.

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.