Jobs at Syneos Health

Lead or support real-world evidence studies by contributing to study design, conducting literature reviews and qualitative interviews, analyzing real-world data, preparing protocols, technical reports, manuscripts, and client presentations, and using statistical software and Microsoft Office to deliver timely, high-quality outputs for life sciences clients.

Manage and coordinate clinical study deliverables, maintain TMF and inspection readiness, assist with interim analyses, vendor selection and management, financial reporting and budget reconciliation, facilitate team training, and support client communications and proposal activities to help meet study milestones.

The Global Clinical Trial Manager oversees the implementation of clinical studies, ensuring compliance, managing sites, and coordinating with vendors while providing oversight and support throughout the trial process.

Perform clinical review of oncology study participant-level data to ensure readiness for milestones (interim/final analyses, submissions). Conduct point-to-point and interpretive checks, generate and track queries, identify safety signals or protocol deviations, liaise with study teams, and follow SOPs to ensure data is clinically valid and submission-ready.

Lead development, negotiation, and management of US site budgets and clinical trial agreements. Negotiate with large academic institutions, draft templates, conduct due diligence (FMV, site justification), manage multiple contracting projects (oncology preferred), update trackers, ensure GCP and SOP compliance, train team members, and support process improvements to enable timely CTA execution.

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.

The Director of Organization Design leads a team to improve organizational effectiveness by partnering with executives, overseeing strategic initiatives, and ensuring scalable, evidence-based solutions that align with business priorities.

Provide clinical and scientific expertise for protocol design, eligibility and endpoint review, rating scale management, rater qualification, training/certification, CRF and eCOA review, and site/investigator support. Perform clinical and statistical analysis of scale/endpoint data, deliver training, contribute to publications and business development, mentor CST members, and support quality control and process improvements.

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.

Conduct site qualification, initiation, monitoring, management, and close-out visits to ensure protocol, regulatory and ICH/GCP compliance. Review source documents and CRFs, manage queries, investigational product handling, ISF/TMF reconciliation, documentation, and support audit readiness. Act as liaison with sites and sponsors, support recruitment/retention, and may train junior staff. Heavy travel (up to 75%).

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

The Director of Epidemiology Pipeline will oversee oncology clinical trials, lead project proposals, manage timelines and budgets, and develop training on epidemiological study designs.

Design and deliver rater training, perform eligibility reviews, analyze endpoint and clinical data, advise on protocol and endpoint strategy, and collaborate cross-functionally to identify risks and protect study integrity for global clinical trials.

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

The Study Manager oversees clinical research studies, ensuring compliance with regulations, managing project teams, and maintaining study deliverables.

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