Jobs at Syneos Health

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.

Perform clinical review of oncology study participant-level data to ensure readiness for milestones (interim/final analysis, submissions). Conduct point-to-point and interpretive checks, generate and resolve queries, identify trends and safety signals, liaise with study team, and follow SOPs to maintain data quality and integrity.

Design and analyze real-world evidence studies using EMR and claims data. Develop SAPs/protocols, apply causal inference and trial-emulation methods, construct external control arms, perform sample size and power calculations, write cohort definitions in SQL, and translate results for HEOR, regulatory, and clinical stakeholders.

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.

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.

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.

Lead sponsor-dedicated biomarker study operations across phases 1-4, coordinating cross-functional teams, vendors, and sample logistics. Manage project delivery (timelines, budget, scope), maintain TMF and study systems, ensure regulatory compliance and inspection readiness, prepare reports, and proactively mitigate operational risks. Support bioanalytical strategy, specimen collection/tracking/analysis, and stakeholder communication.

The Central Risk Manager is responsible for developing and implementing strategies for Risk-Based Quality Management and Monitoring across clinical trials, collaborating with stakeholders, and leveraging data analytics for risk identification and mitigation.

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