Syneos Health

Project Manager

• provide reliable operational support
• maintain accurate documentation
• coordinate with cross-functional teams
• ensure smooth execution of enablement activities
• participate in monthly finance activities such as revenue review, pass-through cost analysis, and invoice validation

Junior Project Specialist, Clinical Experience

Software Engineer

• Develop custom programming code to generate summary tables, data listings, graphs, and derived datasets
• Ensure outputs meet quality standards and project requirements
• Perform validation programming and work with project team members to resolve discrepancies
• Keep project team members informed of programming progress and issues
• Maintain well-organized project documentation
• Manage scheduling and time constraints across multiple projects
• Develop specifications for datasets and outputs of any complexity
• Conduct effective internal meetings
• Direct programming activities of other personnel and monitor progress
• Review project documentation and provide feedback
• Participate in sponsor meetings as a statistical programming representative

Principal Stat Programmer, SDTM, ADAM, TLF

Clinical Research

• Perform medical and scientific data review on haematology clinical trials (indication anticipated myeloma or lymphoma)
• Standard data listing review (data listings, AEs, con meds, etc.)
• May complete patient profile review, standard listing data review, efficacy review and safety narrative review, PD analysis and PD review
• Will support Lead Scientist with scientific data review of clinical trial
• May support with additional CS tasks beyond scope of data review at the discretion of the Lead CS team however the primary role will be scientific data review
• Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan)
• Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans
• Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews
• Authors medical data queries and reviews query responses, approves query closure in association with Medical Director
• May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed
• Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed
• Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met
• Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review
• Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety
• Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner
• Attends at Trusted Process meetings and may participate in internal and external audits
• Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology
• Adheres to all data privacy guidelines, ICH, and GCPs, all enterprise policies, standard operating procedures, work instructions, and project plans
• Adheres to customer policies and standard operating procedures, as required in project plans

Clinical Scientist

Analyst

• Lead system analysis to evaluate existing processes, identify gaps, and recommend improvements for data-driven and application-based solutions.
• Gather and analyze project requirements and specifications from clients and internal stakeholders (technical and non-technical) throughout the project lifecycle.
• Translate business rules and stakeholder needs into actionable analytic and application design specifications leveraging internal and external data sources.
• Provide product support by troubleshooting issues, analyzing root causes, and ensuring timely resolution to maintain product performance and client satisfaction.
• Contribute to application design for client-facing healthcare analytics products (dashboards, apps, widgets, automated reporting) ensuring usability and scalability.
• Manage development activities by coordinating with engineering teams, defining development guidelines, and ensuring adherence to timelines and quality standards.
• Develop production schedules, test plans, documentation, and presentation materials that define project guidelines and milestones.
• Communicate project updates directly to clients through in-person demonstrations, virtual calls, and emails; manage change requests effectively.
• Coordinate internal teams (data engineers, software developers, data scientists, product managers, dashboard developers, business stakeholders) and external resources (e.g., data vendors) to ensure timely delivery.
• Independently prototype analytic tools and resources for proof-of-concept scenarios, troubleshooting, and solution development.
• Manage multiple, complex analytic and application development workstreams and timelines, ensuring outcomes meet or exceed client expectations.
• Mentor and coach junior analysts and team members across the organization.

Principal Analyst

• responsible for governance, configuration, and lifecycle management of RAVE environments
• ensure secure, compliant, and efficient environment provisioning
• act as the primary SME and escalation point for URL-related issues
• partner with Medidata Vendor management, Clinical Programming, and Study Operations
• perform environment readiness checks and coordinate build activities
• author and enforce SOPs/Work Instructions for environment provisioning

Senior Clinical Programmer – Rave, Veeva CDB Admin URL

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiological Practices (GPP) and protocol compliance.
• Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and with guidance develops action plans.
• Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes.
• Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate.
• Demonstrates diligence in protecting the confidentiality of each subject/patient.
• Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
• For the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes.
• Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete.
• Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines.
• Utilizes available hardware and software to support the effective conduct of the clinical project data review and capture.
• Verifies site compliance with electronic data capture requirements.
• May perform investigational product (IP) inventory, reconciliation and reviews storage and security.
• Verifies the IP has been dispensed and administered to subjects/patients according to the protocol.
• Verifies issues or risks associated with blinded or randomized information related to IP.
• Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned.
• Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness.
• Reconciles contents of the ISF with the Trial Master File (TMF).
• Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations.
• Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.
• Supports subject/patient recruitment, retention and awareness strategies.
• Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution.
• For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met.

Clinical Trial Manager – Quality Visits Experience

• Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, with monitoring activities
• Oversees site interactions post activation through site closeout
• May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT)
• Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/Central Monitors) is aware of the contractual obligations and parameters
• Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables
• Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope
• Employs strategic thinking and problem-solving skills to propose and implement risk mitigations
• Participates and presents in key meetings such as Kick Off Meeting
• Serves as an escalation point for communications with investigator site staff and may be required to interact on the phone or in person with principal investigators or other site staff members
• Collaborates with other functional leaders such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery handoffs and meet expected study milestones such as site activation targets, enrollment targets and database lock timelines
• Ensures CTMS, dashboards and other systems are set up and available for use by the clinical team, including overseeing user acceptance testing (UAT) as needed
• Ensures access and audit trail reviews are conducted as required
• Coordinates initial and ongoing training to the study team regarding protocol specificities, Case Report Form (CRF) completion, dashboards, Sponsor Standard Operating Procedures (SOPs), clinical plans and guidelines, data plans and timelines for the study
• Oversees resourcing allocations for CRAs and Central Monitors, site assignments and study team members' conduct, and identifies risks to delivery or quality
• Ensures quality of the clinical monitoring, central monitoring and site management deliverables within a project and maintain proper visibility of its progress by the use of approved systems and / or tracking tools
• Reviews the project oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs),Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to oversee site and patient activities, study team conduct and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits/calls, duration, and frequency) according to plan
• Understands the monitoring strategy required for the study and, where required, participates in the development of the study risk assessment plan
• Is accountable for their assigned clinical team members' understanding, ongoing compliance and delivery according to the stated monitoring strategy, CMP/SMP, and risk plans
• Reviews the content and quality of site and central monitoring documentation (site monitoring calls, site visit reports, site letters, central monitoring reports and pertinent correspondence), to ensure they represent site management activities and conduct and that they appropriately convey any risks to protocol/GCP compliance, trial conduct, patient safety or data integrity
• Document requested revisions and approvals in CTMS
• Ensures these deliverables are provided according to company and/or sponsor specifications, including delivery deadlines
• Interacts with the client and other functional departments related to clinical monitoring, central monitoring and site management activities and deliverables
• Provides status updates on the clinical deliverables and risks to clients, project management and leadership as per departmental or study agreements
• Provides solutions for obstacles in protocol execution and site management.
• Demonstrates understanding of other functions' roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP and country regulations
• Supports Inspection Readiness for clinical trial management scope
• Oversees CRAs and Central Monitors assigned to the study and routinely assesses study-specific process and training compliance, CMP compliance, and identifies emerging risks
• May develop and support execution of corrective action plans at site and study level
• Supports and completes activities to achieve data cut and lock deadlines

Clinical Trial Manager II – Sponsor Dedicated, Monitoring Activities

Research Analyst

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits
• Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions
• Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes
• Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient
• Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site

Clinical Research Associate I

• Serves as a statistical department resource
• Conducts training sessions for new hires
• Directs activities of biostatistics personnel on projects
• Monitors study activities against milestones
• Provides statistical programming support

Senior Principal Biostatistician – Oncology

• Manage project overseeing interdisciplinary clinical research programs
• Act as primary liaison between Company and Customer
• Lead clinical team to ensure quality, timelines, and budget management
• Prepare and present project material at internal and external meetings
• Develop contingency planning and risk mitigation strategies

Senior Project Manager

• Manage interdisciplinary clinical research programs ensuring compliance with regulations
• Act as primary liaison between Company and Customer for project conduct
• Ensure project quality, timelines, and budget management
• Maintain project information on databases and systems
• Prepare project management reports for clients and management
• Develop contingency planning and risk mitigation strategies
• Train and support new Project Managers

Director

• Develop and execute a regional growth strategy to expand Syneos Health’s footprint across emerging biotech and pharmaceutical companies
• Cultivate trusted relationships with C-suite executives, scientific leaders, and investors within the local ecosystem, representing Syneos Health’s integrated capabilities and scientific depth
• Serve as a visible regional ambassador, maintaining a strong presence at industry events, forums, and thought-leadership venues to build brand awareness and credibility
• Proactively identify and shape new opportunities through early engagement, leveraging insights to craft differentiated value propositions tailored to client needs
• Coordinate with BD and Delivery leaders to ensure the seamless translation of opportunities into successful project execution
• Maintain strong situational awareness of regional biotech trends, funding landscapes, and regulatory influences, using this knowledge to anticipate customer needs and market shifts
• Champion operational excellence and delivery readiness across the region, ensuring Syneos Health’s commitments align with client expectations and strategic intent
• Apply the Market Developer playbook principles to balance farming and hunting behaviors—simultaneously nurturing existing relationships and creating new ones that fuel sustainable growth

Managing Director – Regional, US Midsize Accounts

Program Manager

• Develop and execute the enterprise AI strategy and ethical guidelines, aligned with business, operational, and strategic enterprise priorities.
• Parter with Product and Portfolio leads to identify and prioritize high-impact use cases.
• Lead cross-functional teams through the full lifecycle of AI initiatives—from concept to deployment and scaling.
• Partner to establish AI governance, Center of Excellence, KPIs, and delivery frameworks to ensure transparency and measurable impact.
• Manage AI vendor and consulting relationships, including contract negotiations and performance oversight.
• Collaborate with Strategy and Operations teams to refine and adopt effective processes and ways of working.
• Prepare and present reports on Technology Operations performance including key metrics, project status and operational issues.
• Serve as a strategic advisor to executive leadership, translating AI capabilities into business value.
• Drive organizational readiness through education, communication, and change management initiatives.
• Monitor and manage technology budgets including forecasting, expense tracking, and cost control.
• Ensure technology expenditures are aligned with budgetary constraints and financial goals.
• Communicate effectively with stakeholders at all levels including Senior Management to provide updates and resolve issues.
• Identify and manage risks associated with technology operations including security, compliance, and operational risks.
• Analyze operational data to identify trends, issues and opportunities for improvement.

Director, Program Management – Some AI Experience

Executive Assistant

• Provide comprehensive executive administrative support to the BUH and their direct reports, as needed.
• Proactively manage a complex and dynamic calendar, prioritizing meetings and ensuring optimal use of executive time.
• Coordinate domestic and international travel, including itineraries, logistics, and contingency planning.
• Serve as a primary point of contact for internal and external stakeholders, managing communications and meeting logistics as required.
• Manage delegation of approvals for timesheets, expenses, and other administrative workflows.
• Handle highly sensitive and confidential information with discretion and professionalism.
• Arrange, coordinate, and host large-scale global virtual meetings.
• Translate the BUH’s high-level direction, notes, and concepts into clear, concise, and executive-ready PowerPoint presentations.
• Act as point of contact for external meeting attendance and coordination, representing leadership with professionalism and credibility.

Procurement

• Completes tasks required to support end users with the selection, onboarding, oversight and offboarding of Vendors/Vendor services
• Develops knowledge and builds proficiency to support the continual evaluation of Vendor usage, spend and strategic fit
• Provides regular and timely status updates to customers
• Tracks the progress of each new Vendor/Vendor service going through the onboarding process
• Contributes to Vendor contract negotiations and the development of Vendor contracts

Junior Project Specialist, Clinical Experience

Principal Stat Programmer, SDTM, ADAM, TLF

Clinical Scientist

Principal Analyst

Senior Clinical Programmer – Rave, Veeva CDB Admin URL

Clinical Trial Manager – Quality Visits Experience

Clinical Trial Manager II – Sponsor Dedicated, Monitoring Activities

Clinical Research Associate I

Senior Principal Biostatistician – Oncology

Senior Project Manager

Senior Project Manager

Managing Director – Regional, US Midsize Accounts

Director, Program Management – Some AI Experience

Executive Assistant

Sourcing Manager I