Jobs at Syneos Health

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.

Supports global clinical trial feasibility, recruitment and retention planning, enrollment optimization, and in-life trial management. The role gathers and analyzes trial data, develops optimization reports and recruitment plans, coordinates timelines and stakeholder reviews, manages vendors and support materials, monitors enrollment performance, and recommends mitigation strategies. Collaboration spans clinical teams, country stakeholders, legal, analytics, vendors, sites, and community or advocacy partners. Oncology trial experience, particularly in lung or breast cancer studies, is preferred.

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.

Serve as an RBQM and Central Monitoring subject matter expert: assess protocols, lead study-level risk assessments, design RBM/RBQM strategies, leverage centralized monitoring analytics, advise sponsors and stakeholders, mentor colleagues, and drive risk mitigation and quality oversight across global clinical trials.

Support Business Unit Controller by recording monthly revenue, loading and maintaining project budgets in Oracle/Revenue Wizard, preparing monthly actual vs. budget variance and backlog forecasts, drafting financial reports, performing project close-out reconciliations, and monitoring project health (revenues, gross profit, receivables, unbilled). Attend project meetings to capture setup data and ensure forecast accuracy.

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.

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.