Jobs at Syneos Health

Prepares financial reports, budgets, forecasts, utilization analyses, revenue backlog reports, profitability insights, and ad hoc analyses for management. Reviews clinical trial and subject data to build forecasts, identifies data inconsistencies, and supports accurate, timely financial reporting. Requires collaboration with Finance and business stakeholders, strong attention to detail, confidentiality, and the ability to manage multiple deadlines.

The role involves overseeing clinical trials, creating project plans, managing budgets, ensuring compliance with regulations, and developing recruitment strategies.

Analyzes RFPs, assigns subject matter experts, prepares proposal text, budgets, and cover letters, and manages proposals through delivery. Coordinates with contracts, finance, operations, and third parties; updates proposal systems; supports project hand-offs and initiation; and presents budgets in requested formats. The role requires strong organization, analytical ability, communication, attention to detail, Microsoft Office proficiency, and familiarity with clinical development or drug development processes.

The Project Manager II coordinates clinical study timelines, collaborates with teams, ensures compliance with regulations, oversees operational aspects of trials, and develops recruitment strategies for successful enrollment.

Conducts clinical trial site qualification, initiation, interim monitoring, management, and close-out activities in accordance with protocols, ICH-GCP, regulations, and SOPs. Verifies informed consent, source data, clinical records, investigational product handling, electronic data, and site documentation. Manages queries, supports recruitment and audit readiness, communicates with site teams, and tracks project deliverables. Requires UK on-site monitoring experience and travel of up to 75%.

Conducts clinical trial site qualification, initiation, monitoring, management, and close-out activities in compliance with protocols, ICH-GCP, regulations, and SOPs. Reviews source documents, clinical data, informed consent, investigational product handling, and essential trial files. Supports recruitment, query resolution, audit readiness, site training, and study timelines. Serves as a liaison with investigators, sponsors, and project teams, with regular UK travel and potential chart abstraction responsibilities for real-world studies.

Conducts clinical site qualification, initiation, monitoring, management, and close-out activities for UK studies. Ensures ICH-GCP, regulatory, protocol, data integrity, informed consent, investigational product, and documentation compliance. Performs source data review, query resolution, site file reconciliation, recruitment support, audit readiness, and site communications. Manages site-level timelines and action plans, collaborates with sponsors and study teams, attends meetings and training, and may support real-world late-phase chart abstraction and junior staff training.

Conducts clinical trial site qualification, initiation, monitoring, management, and close-out activities. Ensures compliance with protocols, ICH-GCP, regulations, and SOPs; verifies informed consent, source documents, clinical data, investigational product handling, and essential files. Supports recruitment, query resolution, audit readiness, investigator meetings, and site communications while documenting activities and managing site-level timelines. Requires regular travel of up to 75%.

Leads biostatistical activities across clinical studies and programs, serving as the sponsor’s primary statistical contact. Develops and reviews SAPs, TLF specifications, analysis datasets, regulatory submissions, integrated analyses, and clinical study reports. Provides statistical design consultation, regulatory support, quality control, programming oversight, mentoring, DSMB/DMC participation, and cross-functional collaboration. Manages project timelines, supports labeling and benefit-risk analyses, and contributes to proposals and sponsor meetings.

Conducts clinical trial site qualification, initiation, monitoring, management, and close-out activities. Ensures ICH-GCP, regulatory, protocol, informed consent, data quality, investigational product, and documentation compliance. Reviews source records, resolves data queries, maintains trial files, supports recruitment and audit readiness, trains site personnel, and communicates risks and action plans. Requires regular travel of up to 75%.

Leads biostatistical activities across clinical studies and biomarker programs, serving as the primary sponsor contact. Designs advanced genomics and biomarker analyses, develops evaluation plans and statistical analysis plans, oversees programming and reporting, ensures quality and regulatory compliance, mentors biostatisticians, and supports submissions, DSMB/DMC activities, proposals, and sponsor interactions.

Leads sponsor-dedicated oncology clinical research programs across EMEA, managing project delivery, timelines, budgets, quality, regulatory compliance, risks, resources, and client relationships. Coordinates cross-functional teams and conduct partners from study launch through closeout, supports inspection readiness and Trial Master File activities, prepares reports and presentations, mentors staff, and contributes to business development and bid defenses. Travel is approximately 25%.

The posting provides limited role-specific details. As a Senior Clinical Trial Supplies Associate, the position is expected to support clinical trial supply activities within a sponsor-dedicated, life sciences services environment. The role is remote and available to candidates in Poland, Ireland, or the UK, with collaboration across clinical development teams and compliance with applicable regulations.

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.

Provides subject matter expertise in clinical trial risk-based and centralized monitoring strategies. Develops risk assessments, supports RACT finalization, identifies and tracks study risks, advises on mitigation plans, evaluates remote data review tools, facilitates risk findings with cross-functional teams and sponsors, supports Quality Tolerance Limits, delivers training, ensures compliance and inspection readiness, and contributes to monitoring strategy budgets and proposals.

The Principal Biostatistician oversees statistical tasks, mentors staff, prepares analyses, and ensures high-quality deliverables throughout project lifecycle.

The Manager of Biostatistics oversees biostatisticians, ensuring project quality, adherence to regulations, and managing staff development while meeting financial targets.

Lead and execute statistical programming activities including migration to SAS Viya, development of tables/listings/figures and derived datasets, CDISC compliance (SDTM/ADaM/DEFINE.XML), process improvement, mentoring, quality control, regulatory submission readiness, client interfacing, and contributing to SOPs and business development. Ensures documentation, inspection readiness, and adherence to industry standards.

The Principal Statistician oversees biostatistics projects, mentors staff, prepares statistical plans, and ensures quality and regulatory compliance in clinical trials.