Syneos Health

Clinical Scientist

• Work with the Medical Director to develop medical plans
• Engage outside experts, consultants, and advisors to obtain medical/scientific input
• Perform regular and ad-hoc medical review of data listings and visualizations
• Analyze data, identify risks and trends, and document medical reviews
• Author medical data queries, review responses, and approve query closure with the Medical Director
• Assist with patient profile reviews, study-level scientific data reviews, protocol deviation reviews, and Medical Review Summary reports
• Partner with Medical Directors on medical data review and safety review meetings, including slide preparation
• Manage project scope, objectives, deliverable quality, milestones, and timelines
• Serve as primary interface among internal teams, customers, and vendors for medical data and eligibility review
• Collaborate with Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management
• Identify and escalate data integrity, subject safety, deliverable, and scope concerns
• Attend and present at Trusted Process meetings and participate in internal and external audits
• Manage a limited number of direct reports and participate in or conduct interviews

Clinical/Medical Scientist – Oncology, Hematology

• Work with the Medical Director to develop Medical Management, Medical Data Review, and Eligibility Review Plans
• Engage outside experts, consultants, and advisors to coordinate medical/scientific input for medical plans
• Perform regular and ad-hoc medical review of data listings and data visualization
• Analyze data to identify risks and data patterns/trends and document medical reviews
• Identify and resolve medical data review issues
• Author medical data queries, review responses, and approve query closure with the Medical Director
• Assist with patient profile reviews, scientific review of study-level data, protocol deviation review, and Medical Review Summary reports
• Partner with Medical Directors on medical data review and safety review meetings, including slide preparation
• Manage project scope, objectives, deliverable quality, milestones, and timelines
• Serve as primary interface between internal teams, customers, and vendors for medical data review and eligibility review
• Collaborate with study team members to identify risks related to data integrity and subject safety
• Escalate study concerns, at-risk deliverables, and out-of-scope tasks to project leads
• Attend and present at Trusted Process meetings and participate in internal and external audits
• Adhere to data privacy guidelines, ICH, GCPs, enterprise policies, SOPs, work instructions, and project plans
• Manage a limited number of direct reports and participate in or conduct interviews

Clinical/Medical Scientist – Oncology – GI

Clinical Research

• Perform site qualification, site initiation, interim monitoring, site management and close-out visits on-site or remotely
• Ensure regulatory, ICH-GCP/GPP and protocol compliance
• Evaluate site and site staff performance, communicate serious issues, and develop action plans
• Verify informed consent, subject confidentiality, safety, clinical data integrity, protocol deviations and pharmacovigilance issues
• Assess site processes and conduct source document review and medical-record review
• Verify clinical data in case report forms and resolve queries remotely and on site
• Use hardware and software to support clinical study data review and capture
• Verify electronic data capture compliance
• Perform investigational product inventory, reconciliation, storage, dispensing and administration checks
• Review Investigator Site Files and reconcile them with the Trial Master File
• Document monitoring activities and enter observations and action items into tracking systems
• Support subject/patient recruitment, retention and awareness strategies
• Manage site-level activities and communication to meet project objectives, deliverables and timelines
• Act as liaison with project site personnel and ensure assigned sites and team members are trained and compliant
• Prepare for and attend investigator and sponsor meetings and clinical training sessions
• Provide guidance on audit readiness and support audit preparation and follow-up
• Mentor junior CRAs and perform training/sign-off visits as assigned
• Potentially perform clinical operations lead tasks under supervision

Clinical Research Associate

Associate

• Drive the planning and execution of elements of clinical trials in partnership with the Project Lead
• Ensure projects adhere to strict timelines and are delivered within budget
• Serve as subject matter expert for relevant project management tools and systems
• Coordinate internal resources and third parties/vendors for efficient project execution
• Maintain and distribute study-specific financial reports and contribute to study financial health using financial processes and systems
• Conduct ongoing analysis of project performance to drive successful completion of short- and long-term goals
• Document project scope and objectives with relevant stakeholders
• Lead communication between project team members regarding project status and changes
• Document and escalate project risks and issues and drive timely follow-through and resolution
• Maintain systems, project management tools, and methodologies
• Drive quality assurance activities, including audit and internal review preparation, documentation, and resolution of actionable issues
• Oversee tasks and activities by mentoring and coordinating junior team members while operating independently with minimal oversight

Senior Project Associate

Nurse

• Interpret and follow trial protocols, Case Report Forms, off-site manuals, supporting documents, procedures, timelines, and SOPs
• Communicate with the Illingworth research nurse project manager, research nurse manager, site staff, and Principal Investigator
• Maintain accurate trial documentation and electronic data transfers while protecting subject confidentiality and complying with GCP and data protection requirements
• Attend Site Initiation Visits and other multidisciplinary, project management, and client-facing meetings as required
• Coordinate and complete on-site and off-site subject trial visits and ensure procedures, assessments, and data collection comply with the protocol and SOPs
• Administer trial medication and facilitate its safe storage, transfer, and accountability
• Process, package, and dispatch samples while liaising with courier companies and organizations
• Identify potentially eligible patients and support recruitment into clinical trials
• Report adverse events, serious adverse events, and suspected unexpected serious adverse reactions, including required follow-up
• Report suspected misconduct or fraud to Illingworth and associated companies

Freelance Research Nurse

Scientist

• Lead scientific oversight of eCOA implementation, ensuring accurate translation of endpoint scales into digital platforms
• Drive development and review of eCOA specifications with vendors
• Own UAT strategy, including authoring and reviewing test scripts
• Lead end-to-end UAT execution and resolve issues for system delivery and study readiness
• Lead global scale licensing and copyright strategy
• Ensure scale selection, version control, and implementation align with protocol-defined endpoints
• Oversee translation strategy and vendor execution across regions
• Drive consistency across source scales, translations, and eCOA/eCRF implementations
• Design and deliver rater training programs
• Define rater qualification standards and support selection of study-ready site personnel
• Develop and deploy training and certification programs
• Monitor rater performance and lead targeted remediation

Assessment Scientist – Masters in Psychology, Psychometrists

Safety Specialist

• Support Syneos Health’s Clinical Solutions organization
• Collaborate with customers and cross-functional teams across the drug development and commercialization continuum
• Apply a drug development mindset to understand customer needs and shape solutions
• Take initiative and challenge the status quo in a competitive, changing environment
• Perform tasks, duties, and responsibilities assigned by the Company

Senior Safety Specialist

• Become fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual, supporting documents, procedures, timelines, and relevant SOPs
• Communicate with the Illingworth research nurse project manager, Research nurse manager, site staff, and Principal Investigator
• Maintain accurate documentation and electronic data transfers while ensuring subject confidentiality, GCP, and data protection compliance
• Attend Site Initiation Visits and other required meetings
• Coordinate and complete subject trial visits on- and off-site with the RN team
• Complete trial procedures and assessments according to protocol and SOPs and collect accurate data
• Administer trial medication and facilitate safe storage, transfer, and accountability
• Process, package, and dispatch samples while liaising with courier companies and organizations
• Assist with identifying eligible patients and patient recruitment, providing information and support for on- and off-site care
• Report adverse events, serious adverse events, and SUSARs and support follow-up
• Report suspected misconduct or fraud

Research Nurse – Per Diem

Analyst

• Configure studies based on final protocols and operational needs
• Assist IT with developing, testing, evaluating, and implementing new technologies
• Assist users with study and system configuration
• Conduct user training and coaching
• Improve existing configurations based on user feedback and harmonize configuration practices with team members
• Create reports, input screens, and documents to facilitate task execution
• Update configurations to satisfy specific data collection requests from internal and external clients
• Create and modify patient-file templates based on user consultation and feedback
• Ensure contingency-plan documents meet requirements
• Perform other clinical tasks as assigned

Study Configuration Analyst

• Remain fully conversant with the trial protocol, Case Report Forms, off-site manual, supporting documents, procedures, timelines, and relevant SOPs
• Communicate with the Illingworth research nurse project manager, research nurse manager, site staff, and Principal Investigator
• Maintain accurate documentation and electronic data transfer while ensuring subject confidentiality, GCP, and data protection compliance
• Attend Site Initiation Visits and other required meetings
• Coordinate and complete on-site and off-site subject trial visits with the RN team
• Complete trial procedures and assessments according to protocol and SOPs and collect accurate data
• Administer trial medication and facilitate its safe storage, transfer, and accountability
• Process, package, and dispatch samples while liaising with courier companies and organizations
• Identify potentially eligible patients and assist with clinical trial recruitment and patient support
• Report adverse events, serious adverse events, and suspected unexpected serious adverse reactions
• Report suspected misconduct or fraud to Illingworth and associated companies
• Join the talent pipeline for a possible upcoming opportunity rather than a live role

Research Nurse

QA Engineer

• Lead and mentor Quality Engineering teams across multiple projects and initiatives
• Drive automation-first testing practices using Provar for Salesforce platforms
• Define and implement QE strategies aligned with Agile and CI/CD delivery models
• Oversee test planning, automation coverage, regression strategy, and release readiness
• Collaborate with Product Owners and Engineering teams during backlog refinement and sprint planning
• Establish and improve QE governance, standards, and best practices
• Support modernization initiatives including shift-left testing and SDLC/PDLC process improvements
• Ensure proper requirements traceability and defect management practices
• Participate in hiring, mentoring, and performance management of QE team members
• Partner with DevOps teams to integrate automated testing into CI/CD pipelines
• Provide delivery metrics, defect analytics, and executive-level reporting
• Support regulated/GxP validation processes where applicable

Quality Engineering Manager – Playwright Test Automation Experience

Medical writer

• Partner closely with Clinical Scientists on protocols and protocol amendments
• Lead clear and accurate completion of medical writing deliverables
• Manage medical writing activities for individual studies with minimal supervision
• Coordinate medical writing activities across departments
• Lead resolution of client comments
• Write clinical study protocols and amendments, clinical study reports, patient narratives, annual reports, investigator brochures, informed consents, plain language summaries, periodic safety update reports, clinical development plans, IND submissions, integrated summary reports, NDA and eCTD submissions, journal manuscripts, abstracts, posters, and presentations
• Follow ICH E3 guidelines, company SOPs, client standards, approved templates, authorship requirements, and style guides
• Coordinate quality and editorial reviews and manage source documentation
• Lead team document reviews and act as an internal peer reviewer
• Review statistical analysis plans and table/figure/listing specifications
• Collaborate with clients and data management, biostatistics, regulatory affairs, and medical affairs teams
• Perform online clinical literature searches and comply with copyright requirements
• Identify and resolve issues, escalating as appropriate
• Provide technical support, training, and consultation
• Mentor and lead less experienced medical writers
• Develop expertise in industry topics and regulatory requirements
• Monitor budgeted hours and communicate status and changes to medical writing leadership
• Complete required administrative tasks and other assigned duties

Sponsor Dedicated Protocol Medical Writer II/Sr

Software Engineer

• Design, write, validate, and maintain clinical programming software using Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, and supporting tools
• Generate and maintain documentation for annotated CRFs, database creation, coding configuration, edit checks, imports, exports, listings, and custom reports
• Coordinate and lead development activities for clinical programming projects
• Participate in project meetings, solve problems analytically, focus on deliverables, provide feedback, and escalate issues affecting dates, scope, or budget
• Provide technology support to clinical programming staff, Project Analysts, Data Managers, and related teams
• Provide application administration and technical support as a subject matter expert on core business packages
• Conduct senior reviews of study-level, program-level, and multi-study core deliverables
• Attend sponsor audits and assist with in-progress audits
• Review study budgets, monitor scope against actual work, and manage change orders
• Monitor applications for workflow alerts, system errors, and performance issues; provide second-tier help desk support
• Perform system integration, application updates, and user acceptance testing
• Provide leadership, training, guidance, and support to department members
• Collaborate with clients, peers, lead programmers, project teams, and requestors to finalize specifications
• Lead assigned-study activities at Quick Start Camps
• Lead clinical programming activities across three to ten concurrent studies
• Manage project resources and alert management to delivery and resourcing needs
• Maintain broad knowledge of clinical programming and clinical data management through literature, training, and professional meetings

Senior Clinical Programmer – Rave

General

• Provide project and operational support to the clinical team
• Assist with clinical project coordination and administrative activities
• Support study-related processes and documentation
• Collaborate with cross-functional stakeholders
• Adapt as departmental needs and study priorities evolve
• Help identify and resolve operational issues proactively

Project Specialist – Sponsor Dedicated

Data Analyst

• Deliver data-driven insights that inform talent strategies, workforce planning, and organizational decision-making
• Support the design, development, and delivery of workforce analytics, dashboards, reports, forecasting models, and predictive insights
• Serve as a Subject Matter Expert for Syneos HR data, workforce metrics, systems, and reporting structures
• Partner with HRBPs, COEs, business leaders, and cross-functional teams to translate business challenges into analytical solutions
• Conduct advanced workforce analysis across the employee lifecycle, including talent acquisition, workforce planning, performance, engagement, retention, turnover, diversity, and organizational effectiveness
• Develop workforce forecasts and scenario-based analyses for hiring strategies, capacity planning, and business decision-making
• Support predictive analytics models related to attrition, hiring demand, workforce trends, and talent outcomes
• Analyze and integrate data from Workday, Power BI, Databricks, survey platforms, Excel, and other enterprise systems
• Build, enhance, automate, and maintain dashboards, scorecards, and recurring reports
• Present actionable insights and recommendations through data storytelling and visualization
• Support Business Development and Proposal activities with workforce analytics, market intelligence, staffing assumptions, and data-driven insights
• Support talent reviews, succession planning, performance management, engagement surveys, compensation analysis, and strategic workforce planning
• Partner with HRIS, IT, and data teams to improve data governance, data quality, metric definitions, and reporting consistency
• Automate manual reporting processes and streamline workflows
• Develop and maintain reporting documentation, metric definitions, data dictionaries, process maps, and user guides
• Promote data literacy and self-service analytics
• Share knowledge, mentor junior analysts, solve complex business problems, and deliver workforce analytics solutions