Worldwide Clinical Trials

Clinical Research

• Review and assess clinical data
• Translate complex data into clear insights
• Communicate clinical findings to teams and clients
• Support development of clinical study reports

Clinical Scientist – Oncology

Medical Director

• Serves as Global Lead Medical Monitor (GLMM) for pan-regional and/or global trial(s)
• Provides therapeutic and protocol-specific training to project teams
• Contributes medical input into the design of clinical development programs
• Maintains a high level of competence with assigned projects
• Assists in the annual attainment of departmental revenue targets

Medical Director, Medical Affairs – Neurology

Vice President

• Provide executive oversight across multiple clinical research programs, complex submissions (e.g., NDAs), and global client relationships.
• Set strategy and lead the global Biostatistics and Programming department, ensuring high-quality, compliant, and timely delivery.
• Oversee operational execution within contractual scope, serving as an escalation point for project and client issues as needed.
• Recruit, develop, mentor, and retain biostatistics and programming leaders and staff, with full accountability for performance management and workforce planning.
• Establish, maintain, and optimize department SOPs, processes, metrics, best practices, and utilization.
• Provide advanced technical leadership to support statistical analysis, programming, and reporting solutions across studies and programs.
• Drive financial oversight for the department, including budgeting and non-billable travel approvals.
• Partner with commercial and business development teams to support proposals, bids, and client presentations.
• Provide strategic input into technology and future-state capabilities.
• Represent the department and company in cross-functional forums, client meetings, bid defenses, and industry events.
• Act as a biostatistics and programming champion, promoting innovation, quality, and operational excellence across the organization.

Vice President, Biostatistics and Programming

• Provide leadership and direction to clinical site management team members from study start through to closure
• Serve as Site Management’s primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to Primary Sponsor Contact
• Manage monitoring deliverables to achieve the study budget and identify out-of-scope activities

Clinical Trial Manager – CNS

• Partner with cross-functional Study Teams (Medical, Biostatistics, Data Management) to develop and execute data review plans, ensuring accurate collection and reporting of protocol-defined endpoints.
• Perform ongoing review and interpretation of clinical data (efficacy and safety) across listings and visual analytics, identifying trends and generating actionable insights.
• Monitor and analyze safety events across studies and programs, supporting risk identification, escalation, and informed decision-making.
• Communicate and present clinical findings, trends, and recommendations to Study Teams, Medical leadership , and clients; contribute to strategic discussions and study modifications.
• Support development of key deliverables, including clinical study reports (CSRs), regulatory documents (e.g., INDs, NDAs/BLAs, IBs), and data summaries for SRCs, DSMBs, and internal review meetings.
• Collaborate on CRF design, data quality processes, and EDC query management; identify protocol deviations and ensure data integrity in partnership with internal teams and vendors.
• Contribute to study execution and continuous improvement efforts, including dashboard/UAT support, study documentation, scientific writing (e.g., narratives, abstracts), and mentoring of junior staff.

Clinical Scientist

Project Manager

• Senior Project Manager (SPM) is responsible for the overall coordination and management of clinical trials from start-up through closeout activities.
• Directs the technical, financial and operational aspects of the projects -- thus securing the successful completion of clinical trials.
• Works with major functional area leads to identify and evaluate fundamental issues on the project, interpret data on complex issues, make good business decisions and ensure solutions are implemented.
• Works to ensure that all project deliverables meet the customer’s time/quality/cost expectations

Senior Project Manager

Proposal Manager

• Develop robust proposals, leading the writing, coordination, and presentation of responses in Word, PowerPoint, and other systems or formats
• Work with Account Directors and SMEs to effectively manage the proposal development process
• Actively participate in project strategy discussions, ensuring product and service offerings are clearly articulated in proposals
• Proofread, edit, rewrite, and revise documents to ensure readability, consistency, accuracy, and relevance
• Meet proposal deadlines by establishing priorities and target dates for information gathering, writing, reviews, approvals, and signatures
• Collaborate with SMEs to gather information and customize content
• Provide a high level of mentorship to junior proposal writers, including onboarding, training, and ongoing learning and development

Senior Proposal Manager – Writing

Research Analyst

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
• Conduct study initiation visits (SIVs)
• Ensure compliance with obtaining informed consent and reporting potential safety-related events
• Adhere to all applicable regulatory requirements

Senior Clinical Research Associate – Oncology

Operations

• Fulfil the TMF Approver and/or TMF QC Reviewer roles as defined by relevant SOPs
• Process, review, and resolve rejected TMF documents for complex studies
• Prepare periodic TMF Quality Control checklists for Project Team review
• Perform TMF Quality Control to ensure adherence to regulatory and industry best practices
• Work with Electronic Document Management and eTMF Systems to review Essential Documents

Associate II, TMF Operations

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
• Conduct study initiation visits (SIVs)
• Ensure compliance with obtaining informed consent and reporting potential safety-related events

Senior Clinical Research Associate

Data Scientist

• Manage each of the data management projects to which assigned; provide leadership to the corresponding data management teams.
• Represent WCT in all dealings with Sponsors with respect to the Data Management aspects of the projects to which assigned.
• Liaise with the Director, Data Management at regular intervals to discuss progress and any issues outstanding.
• Take responsibility for staff training for all projects to which assigned; both direct involvement in training and supervision of staff assigned to training.
• Ensure that all data management operations are conducted to WCT SOPs; contribute to the ongoing revision/improvement of these SOPs.
• Create and review project specific documentation for assigned trials, i.e. the Data Management Plan and the Data Management File.
• To ensure that adequate QC checks (including spot checks) and Database Quality Assessments on the clinical databases of assigned projects.

Senior Clinical Data Manager

• Perform RMC Lead Activities for 1-3 Studies
• Support TMF set-up, coordinate ‘Requests for Sites to be added in eTMF’ between Project Teams (PT) and eTMF administrators
• Review eTMF access and coordinate updates, as necessary
• Provide Subject Matter Expert (SME) support for Project Teams and Sponsor related to TMF
• Oversee the QC process and make sure the RMC is on track (compliant with timelines and documentation) and follow up on non-compliance accordingly
• Prepare, maintain, and share TMF metrics and spreadsheets for assigned studies with Project Teams and Sponsors
• Review TMF Key Performance Indicators (KPIs) and ensure that TMF KPIs are in compliance
• Support Regulatory and Sponsor audits and audits finding resolution, where necessary

Senior Associate I, TMF Operations

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
• Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort
• Conduct study initiation visits (SIVs)
• Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements

• Provide strategic leadership and executive oversight for the company’s global Data Management function.
• Set the vision, operational framework, and standards that enable efficient, compliant, and high-quality data delivery across the organization.
• Oversee department strategy, execution, and continuous improvement, ensuring real-time, efficient data flow that results in clean, analyzable databases.
• Lead and develop high-performing teams, establishes and maintains robust processes and SOPs, and ensure readiness for client and regulatory audits.
• Partner closely with cross-functional and executive stakeholders, evaluates key performance indicators, supports business development efforts, and maintains financial oversight of the department.
• Hold full accountability for the recruitment, retention, and development of Data Management talent.
• Act as the executive escalation point for project and client issues, fostering strong partnerships and positive client relationships.
• Provide strategic input into business development, including RFP responses, bid defenses, and client presentations.
• Represent the Data Management function internally and externally, including cross-functional forums, client meetings, and industry events.

Vice President, Data Management

• Provide leadership and direction to clinical site management team members from study start through to closure
• Serve as Site Management primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to: 1. Primary Sponsor contact 2. Investigator and Bid Defense Meetings 3. Internal and External study team calls 4. Project-specific Audits / Inspections
• Manage monitoring deliverables to achieve study budget and identify Out of Scope Activities
• Oversee compliance to the Clinical Monitoring Plan, including site visits, outstanding trip reports and visit follow up letters