Jobs at Syneos Health

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

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.

Reviews clinical trial data for quality, consistency, and completeness; identifies and resolves discrepancies in EDC systems; cross-checks patient data across EDC, laboratory, and safety databases; supports data cleaning, interim analyses, and database lock activities; monitors site data entry and escalates risks; collaborates with clinical, data management, and operations teams; and ensures compliance with GCP, study protocols, and regulatory requirements.

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.

Leads biostatistical activities across clinical trial projects from protocol through clinical study report. Develops and reviews statistical analysis plans, programming specifications, datasets, and study outputs; mentors biostatisticians; oversees quality control, timelines, regulatory submissions, and sponsor interactions. May support DSMB/DMC activities, regulatory meetings, proposals, and statistical programming. Requires extensive clinical-trial experience, graduate-level biostatistics training, and R proficiency.

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.

Manage a multifunctional clinical operations/data review team in an FSP environment, ensuring quality deliverables, KPI compliance, customer issue escalation, resource planning, revenue impact, and people leadership including performance management, training, workload oversight, and staff development.

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.