Jobs at Syneos Health

Lead preparation, negotiation, execution, and archival of site-specific clinical trial agreements and investigator budgets for multi-country studies. Manage contract processes, collaborate with legal/finance/operations, track SSU milestones, identify and mitigate contract risks, mentor junior staff, and support business development and SOP/template improvements.

Support design and execution of retrospective and prospective real-world evidence studies, conduct literature reviews and qualitative research, analyze and interpret real-world data, develop protocols, reports, manuscripts, and client presentations, and use Microsoft Office and statistical software to produce high-quality deliverables under senior guidance.

Lead development, negotiation, and management of US site budgets and clinical trial agreements for pharma and vaccine studies. Negotiate with large academic institutions, conduct due diligence (FMV, site justification), maintain trackers and CTMS, ensure compliance with GCP and SOPs, prioritize multiple contracting projects (oncology preferred), train team members, and drive process improvements.

Manage clinical study scope, schedule, cost and deliverables across internal teams, vendors and sites. Maintain TMF, support interim analyses and study closeout, assist vendor contracting and change orders, prepare financial and metric reports, support proposal/customer interactions, and facilitate team training to ensure regulatory compliance and project milestones are met.

Design and analyze real-world evidence studies using EMR and claims data to support clinical development, HEOR, regulatory and market access. Apply causal inference, trial emulation, external control strategies, survival analysis and ML methods; write SAPs and protocols; perform cohort definition, sample size/power calculations, data debugging, and translate results into study reports and presentations.

Lead development, negotiation, and management of US site budgets and clinical trial agreements for pharma and vaccine studies. Negotiate with large academic institutions, manage risk and escalations, develop templates, maintain trackers, train team members, and support process improvements. Requires Excel and CTMS proficiency and cross-functional project leadership; oncology experience preferred.

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.

Lead and deliver regulatory clinical documents (protocols, CSRs, narratives, IBs, eCTD/IND/NDA submissions, manuscripts). Ensure adherence to ICH E3 and SOPs, coordinate reviews, review SAPs/TFL specs, mentor junior writers, liaise with biostatistics/regulatory/data teams, perform literature searches, manage quality and budgets, and resolve client comments. Occasional travel (<25%).

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 roles include developing medical plans, reviewing medical data, collaborating with study teams, and ensuring compliance with protocols and guidelines.

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 interdisciplinary clinical research studies, ensuring compliance with regulations, managing project finances, coordinating activities, and leading project teams to achieve study goals.

The Study Manager oversees and manages interdisciplinary clinical research studies, ensuring compliance with regulations, financial performance, and project deliverables, while acting as a liaison between the company and customers.

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

Manage interdisciplinary clinical research studies ensuring compliance with GCP, overseeing project delivery, financial performance, and quality management while liaising with clients.

Manage and oversee interdisciplinary clinical research studies, ensuring compliance with regulatory requirements and project deliverables while maintaining financial performance and client relationships.

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.