Jobs at Syneos Health

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.

Conducts site qualification, initiation, monitoring, management, and close-out visits for clinical studies. Ensures ICH-GCP, regulatory, protocol, informed consent, data integrity, investigational product, and site documentation compliance. Performs source document review, query resolution, and audit readiness activities; supports recruitment, retention, and investigator relationships. Manages site-level timelines and communications, may mentor junior CRAs, and supports real-world late-phase activities including chart abstraction, data collection, and country-level informed consent development.

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.

Conduct real-world data analyses using SAS or R and commercial claims and EHR databases. Build longitudinal study cohorts, define baseline and outcome variables, apply epidemiologic methods, perform statistical tests, regression and survival analyses, assess data quality, review protocols and statistical analysis plans, and program tables, figures, and listings. The role requires advanced biostatistics or epidemiology expertise and strong communication skills.

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.

Oversee biostatistical activities, mentor staff, prepare statistical plans, ensure quality control, and manage multiple clinical projects while interfacing with regulatory agencies.

The Executive Assistant provides high-level administrative support to the Business Unit Head, managing calendars, travel, communications, and preparing executive presentations. Skills needed include organization, discretion, and strong communication.

Ensure effective clinical research operations, monitor study progress, adhere to regulations, and coordinate communication with clinical trial participants.

Lead statistical planning and delivery for clinical studies using R and RShiny, mentor biostatistics staff, prepare SAPs and programming specifications, perform quality control, support submissions and regulatory interactions, and develop/maintain R-based visualization apps and infrastructure.