Jobs at Syneos Health

Manages Clinical Data Science staff, client relationships, project delivery, budgets, quality, utilization, training, and regulatory readiness across clinical studies. Oversees clinical data science activities from project launch through closeout, supports audits and CAPAs, monitors data quality and risk, mentors team members, contributes to business development, and helps develop tools, SOPs, and processes for clinical data management.

Provides project and operational support for clinical teams, including study coordination, documentation, meeting coordination, follow-up activities, and issue resolution. Collaborates with cross-functional stakeholders and adapts to changing study requirements. Requires entry-level clinical research experience, familiarity with Veeva Vault and clinical trial management systems, strong organization and problem-solving skills, independence, and proficiency in Microsoft Excel.

Provides project support and administrative coordination across clinical research initiatives. Supports patient engagement, recruitment, and retention strategies for oncology and cardiology studies, collaborates with cross-functional teams, advances process improvements, and uses AI tools and automation to improve efficiency. Requires clinical research or project coordination experience in a pharmaceutical, CRO, or related environment.

Manages clinical research sites throughout study start-up, monitoring, data review, compliance, documentation, recruitment, and closeout activities. Ensures adherence to protocols, SOPs, local regulations, GPP, and ICH-GCP. Maintains study tracking systems and essential documents, supports audit readiness, resolves site issues and data queries, and communicates with investigators, sponsors, and project teams. The role requires substantial travel, strong organization, effective communication, and the ability to manage multiple studies and priorities.

Leads global clinical trial site contract and investigator budget negotiations, including contract execution, payment terms, financial attachments, escalation management, risk mitigation, and stakeholder coordination. Serves as a subject matter expert for sponsors and internal teams, develops negotiation strategies, oversees status reporting, trains staff, supports process improvements, and contributes to business development. Minimal travel of up to 25% may be required.

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.

Leads global inflammation clinical trials for a biopharmaceutical sponsor, overseeing study start-up, enrollment, conduct, timelines, budgets, vendors, CRO interactions, data reviews, risk mitigation, trial documents, and cross-functional teams. Provides guidance and training to investigators, vendors, and study personnel; organizes trial meetings; supports CRO selection, recruitment, and team development; and coaches project team members.

Provide medical and scientific oversight for immunology clinical studies, including medical plan development, medical data and safety review, query authoring, cross‑functional collaboration, and documentation to identify risks and ensure data integrity and patient safety.

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 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.

Leads early-phase and clinical pharmacology programs as a medical subject matter expert and governance lead. Oversees medical staff, clinical studies, protocol development, safety and pharmacovigilance input, therapeutic training, data review, and customer relationships. Supports business development through RFP/RFI responses and bid defenses, contributes to development plans and regulatory submissions, engages external experts, and represents the company at scientific and industry meetings.

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.

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.

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 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.

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.

Support proposal lifecycle for CRO/pharmaceutical RFPs: receive and analyze RFPs, draft and edit proposal text, budgets and cover letters, obtain third-party quotes, manage proposal stage gates, coordinate handovers, and work with contracts, finance and operations to initiate projects.

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.