Jobs at Syneos Health

Leads clinical trial management activities, including site oversight, clinical and central monitoring, risk mitigation, compliance, team resourcing, training, documentation quality, and milestone delivery. Oversees CRAs and Central Monitors, manages clinical trial systems and tools, communicates risks and status to clients and leadership, supports inspection readiness, and coordinates cross-functional execution across international studies. May lead complex trials, mentor CTMs, and travel approximately 20%.

Leads end-to-end eCOA delivery across global clinical trials, including system design, configuration, validation, UAT, deployment, maintenance, vendor oversight, translations, licensing, risk management, and inspection-ready documentation. Serves as the primary liaison among sponsors, vendors, and cross-functional clinical teams while managing timelines, deliverables, quality, multiple studies, and stakeholder communications.

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.

Lead development, validation, and optimization of bioanalytical methods; analyze and interpret data; write/review SOPs and technical reports; drive lab process improvements; train, mentor, and potentially supervise scientific staff; coordinate resources, evaluate instruments, and ensure compliance with corporate and regulatory requirements.

Manages interdisciplinary oncology clinical research studies from launch through closeout, ensuring GCP, SOP, regulatory, quality, timeline, and budget compliance. Serves as the primary client liaison, coordinates study partners, oversees project plans, TMF completeness, databases, inspection readiness, risk mitigation, reporting, and financial performance. Builds client relationships, supports business development and bid defenses, and may line-manage project management or clinical monitoring staff.

Conducts site qualification, initiation, monitoring, management, and close-out activities for clinical studies. Ensures compliance with protocols, ICH-GCP, regulations, informed consent, data quality, investigational product procedures, and essential document requirements. Reviews source documents, resolves queries, supports recruitment and retention, maintains audit readiness, manages site communications and timelines, and collaborates with sponsors and study teams. Requires regular travel of up to 75% and may support real-world late-phase studies, chart abstraction, site identification, and junior staff training.

Lead operational execution of a complex Phase 2b inflammation trial from start-up through closeout. Independently manage day-to-day study operations, timelines, risks, vendor/CRO oversight, cross-functional leadership, study documentation, budget tracking, and training. Drive issue resolution, mentor junior staff, and implement process improvements in a sponsor-dedicated, fast-paced environment.

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.

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