Fortrea

Medical Director

• Provide medical leadership and strategic support while partnering with clients and cross-functional teams
• Strengthen relationships and drive successful clinical development programs
• Provide oversight, mentorship, and guidance to team members
• Contribute to Global Clinical Operations initiatives
• Contribute to Company policies involving medical, safety, and therapeutics
• Participate in Company-wide process improvement activities
• Lead staff within the therapeutic area
• Lead initiatives involving physicians within and across the therapeutic area
• Contribute to the vision and strategic direction of the therapeutic area
• Develop training modules and materials and provide disease-state and protocol-specific training
• Participate in training on drug development and Good Clinical Practice guidelines
• Provide drug development expertise to medical strategy and execution of client programs
• Develop, review, and revise protocols, case report forms, training materials, project-specific tools, analysis plan designs, clinical trial reports, and new drug applications
• Provide medical and scientific expertise to project teams
• Act as Medical Monitor/study support for early clinical trials
• Perform medical and safety monitoring on assigned projects
• Interact with interdepartmental teams and external consultants
• Participate in feasibility discussions for project proposals
• Participate in project risk assessment activities
• Assist with Data Safety Monitoring Board activities when needed
• Provide clinical and medical expertise to other Fortrea departments
• Contribute to scientific and strategic leadership of a therapeutic area
• Perform other assigned duties and responsibilities

Senior Medical Director, MD

Clinical Research

• Provide a high standard of care for participants in Phase I clinical trials
• Respond to emergency situations according to clinical research standards
• Monitor clinical study sites, including routine monitoring and close-out visits
• Maintain study files and conduct pre-study and initiation visits
• Liaise with vendors
• Manage study sites according to project plans
• Ensure study staff receive proper materials and instructions
• Verify informed consent procedures and protocol requirements comply with regulatory requirements
• Verify integrity of Case Report Form and other data submitted through source-document monitoring
• Monitor data for missing or implausible information
• Manage registries and conduct feasibility work when requested
• Complete Serious Adverse Event reporting, narratives, reports, and follow-up
• Perform CRF review, generate and resolve queries using Fortrea or client data management systems
• Assist with training new employees through co-monitoring
• Coordinate designated clinical projects as a Local Project Coordinator
• Act as a local client contact when assigned
• Perform other duties assigned by management

Clinical Research Associate II, Phase I

Business Development Rep

• Develop and execute account plans and strategic partnerships within assigned accounts of greater size and complexity
• Provide competitive intelligence and identify cross-business-unit opportunities
• Partner with Client Services to support pricing, margin, and deal-structure decisions
• Collaborate across business units to identify, position, and win multi-unit opportunities
• Participate in corporate account teams to strengthen key client relationships
• Achieve or exceed annual sales targets for assigned accounts
• Establish, grow, and manage client relationships at appropriate decision-making levels
• Execute client call plans, follow up on leads, and support an established client base
• Position the business unit's capabilities and differentiation
• Manage opportunity pipeline, forecasting, and required territory documentation
• Set and manage customer expectations to drive satisfaction and retention
• Lead client presentations, support proposal development, and host client visits
• Provide regular sales activity updates to management
• Perform all other duties as needed or assigned

Business Development Director II – Early Phase

• Develop and execute business development strategies across a broader portfolio of high-priority accounts
• Create and manage strategic account plans and partnerships with key, high-value accounts
• Analyze market trends, customer needs, and competitive intelligence to identify new opportunities
• Achieve or exceed annual sales targets through senior-level client engagement and strategic networking
• Build, maintain, and expand client relationships to drive long-term account value
• Position the business unit's capabilities and differentiation
• Evaluate quotations and collaborate with Client Services to determine pricing and margins
• Own opportunity management, pipeline accuracy, and forecasting
• Drive internal communication and maintain territory and client documentation
• Contribute to proposal development and lead client presentations
• Leverage industry insights and existing relationships to generate new business opportunities
• Scale and diversify the client base through enterprise-level business development strategies
• Drive sustainable revenue growth, enhance competitive positioning, and deliver measurable business outcomes across the portfolio
• Perform all other duties as needed or assigned

Senior Business Development Director – Early Phase

Vice President

• Define and lead execution of the global Therapeutic Area strategy aligned with enterprise objectives and client needs
• Translate Therapeutic Area science, regulatory trends, and market dynamics into scalable medical service offerings and execution roadmaps
• Provide insights, analysis, and recommendations for enterprise investment priorities, operating model evolution, and growth strategy
• Serve as senior scientific partner to clients in senior interactions and governance forums
• Engage executive stakeholders across medical, safety, data management, regulatory, operations, project management, and commercial functions
• Lead or participate in scientific governance forums and provide medical oversight for complex or high-risk activities
• Serve as final escalation point for complex medical, scientific, ethical, and regulatory decisions
• Ensure scientific quality, compliance, integrity, patient safety, and data integrity
• Lead and mentor senior Therapeutic Area medical leaders, including leadership development and succession planning
• Coach and advise Regional Heads to align regional execution with global strategy and drive consistent quality and performance
• Support enterprise-wide talent, culture, and organizational effectiveness initiatives
• Partner cross-functionally with Clinical Operations, Regulatory, Commercial, Strategy, and Data teams
• Drive innovation in medical services, evidence generation, and engagement models, including precision medicine, immuno-oncology, real-world evidence, digital health, and Advanced Therapeutics
• Represent Fortrea externally through industry engagement, publications, presentations, and panel participation
• Oversee assigned programs, ensuring quality and compliance and escalating risks
• Support service development, technical positioning, proposals, bid defenses, and client solution development
• Provide clinical and scientific input to due diligence activities
• Own delivery excellence and scientific quality across assigned programs and clients
• Travel up to 2–3 trips per month, including domestic and/or international travel
• Perform other duties as needed or assigned

Vice President, Global Therapeutic Area Leader, Oncology

• Serve as the technical leader on all data management aspects for projects, including start-up, maintenance, and completion activities
• Develop global Data Management Plans and Quality Management Plans
• Identify and implement solutions to project data management issues and concerns, including proactive prevention strategies based on metrics and forecasts
• Serve as project and client liaison, managing and providing project-specific data management status, cycle time, and productivity metrics
• Coordinate and participate in development of the clinical data model and/or database design and annotate CRFs/eCRFs
• Review data acquisition conventions, data review guidelines, and diagnostic specifications
• Coordinate development and testing of data management system edit/data validation checks, diagnostics, and special listings/procedures
• Collaborate with clinical, programming, statistics, CDM technical support, drug safety, and other project and specialty teams
• Lead advanced planning and risk management, including issue escalation and resource management
• Oversee technical performance of data review project staff and delivery of quality data on time and on budget
• Assist with goal creation and performance review assessments for data review project staff
• Maintain technical data management competencies through internal and external training seminars
• Ensure project staff are trained and adhere to project-specific and global standardized data management processes
• Identify process and efficiency improvements and implement solutions
• Support achievement of project revenue and operating margin targets for data management activities
• Support business development through data management time and cost estimates and presentations to potential clients

Senior Clinical Data Manager – FSO

• Lead/support Phase 1–3 clinical studies
• Be accountable for clinical/scientific execution of protocols
• Serve as clinical point of contact for scientific issues and questions for internal and external stakeholders, including IRBs and sites
• Act as scientific lead on Clinical Trial Teams
• Design trials and develop endpoints in collaboration with Clinical Development
• Collaborate with medical writing on trial-results communications for investigators
• Lead Medical Monitoring activities, including development of the Medical Monitoring Plan, SAE report review, monitoring data issues, and central lab reports
• Set up/support SAC, DMC, and adjudication committees
• Provide scientific input to study management for EDC, DRP, and CRF activities
• Collaborate on protocols and amendments, participate in governance committee review, author protocol clarification letters, and reconcile/review protocol deviations for the CSR
• Mentor other Clinical Scientists

Senior Clinical Scientist – Immunology

• Provide a high standard of care for participants in clinical trials
• Respond to emergency situations according to clinical research standards
• Conduct routine monitoring and close-out of clinical sites
• Maintain study files
• Conduct pre-study and initiation visits
• Liaise with vendors
• Manage study sites according to project plans
• Ensure study staff receive proper materials and instructions to safely enter patients into the study
• Verify informed consent procedures and protocol requirements comply with applicable regulatory requirements
• Ensure data integrity in Case Report Forms and other data collection tools
• Monitor data for missing or implausible data
• Manage study registries and undertake feasibility work when requested
• Complete Serious Adverse Event reporting, narratives, reports, and follow-up
• Perform CRF review and query generation and resolution using Fortrea or client data management systems
• Assist with training new employees through co-monitoring
• Coordinate designated clinical projects as a Local Project Coordinator, with supervision where applicable
• Act as a local client contact when assigned
• Perform other duties as assigned by management
• Travel frequently to client and site locations, including occasional domestic and international travel

• Provide ongoing in-depth analysis and scientific input into development and execution of protocols and clinical development plans
• Work with the medical/scientific/regulatory team to solve medical, scientific, clinical, and regulatory problems
• Serve as a resource for the Medical Monitor by tracking and reviewing study-specific safety data to identify safety trends
• Act as liaison among the Medical Monitor, study sites, Fortrea project staff, and Sponsors regarding protocol and study-related questions
• Document, track, and follow up on study-related issues
• Review and evaluate CPS proposals and provide clinical and scientific support
• Draft study outlines and designs and provide guidance on early clinical development strategies
• Establish and maintain affiliations with the Fortrea and larger scientific community
• Provide rationale and input for including biomarkers or other lab markers in Proof-of-Concept studies
• Attend Kick-off Meetings, SIVs/Investigator Meetings, and Team Meetings
• Support training in key medical/scientific areas
• Ensure medical and safety issues discussed in team meetings are resolved by the Medical Monitor
• Support CPS Medical Monitors in tracking and documenting Inclusion/Exclusion criteria and protocol-related questions and answers
• Perform other related duties as assigned

FSP Clinical Scientist III / Medical Science Liaison

• Provide a high standard of care for participants in clinical trials and respond to emergency situations based on clinical research standards
• Perform all aspects of study site monitoring, including routine monitoring and close-out of clinical sites
• Maintain study files and conduct pre-study and initiation visits
• Liaise with vendors and perform other assigned duties
• Manage study sites according to project plans
• Ensure study staff receive proper materials and instructions to safely enter patients into studies
• Verify informed consent procedures and protocol requirements comply with applicable regulations
• Ensure data integrity in Case Report Forms and other data collection tools by carefully monitoring source documents
• Monitor data for missing or implausible information
• Manage clinical trial registries and conduct feasibility work when requested
• Complete Serious Adverse Event reporting, including reports, narratives, and follow-up
• Independently review CRFs and generate and resolve queries using Fortrea or client data management systems
• Assist with training new employees through activities such as co-monitoring
• Coordinate designated clinical projects as a Local Project Coordinator, with supervision where applicable
• Act as a local client contact when assigned

Clinical Research Associate 2

Project Manager

• Acts as the primary client lead for complex clinical studies or programs
• Drives operational delivery across multiple vendors and teams
• Develops and executes risk-management strategies
• Resolves escalated project issues
• Provides line management and talent development for project management staff
• Serves as primary client contact for assigned clinical studies or programs
• Develops strategies to manage risk and improve operational execution
• Oversees line management and talent development of Individual Contributors and/or Managers of Project Managers
• Builds stakeholder relationships and expands client portfolios
• Leads project teams through design, implementation, tracking, and maintenance of project plans
• Ensures adherence to professional standards, SOPs, contracted timelines, and budgets
• Manages TMF Index & Plan, audit readiness, and TMF delivery when contracted by the client
• Leads quality control and risk assurance activities
• Fosters positive client experiences through communication and collaboration
• Manages strategic client relationship documents, including charters, MSA negotiation, rate card input, operations and quality plans
• Initiates process improvement to address variance
• Designs delivery strategy for large-scale bid defense and performs business development activities
• Attracts, selects, onboards, develops, and retains high-performing talent
• Strengthens talent bench and succession
• Performs other duties as assigned

Director, Project Management – Rare Disease & Pediatrics

Call Center Representative

• Support participant recruitment through planning and execution of recruitment strategies using media and community outreach
• Train new employees
• Liaise with the Recruitment Supervisor, Screening Supervisor, Physicians, and Study/Project Managers
• Provide backup for Clinical Pharmacology Recruitment SharePoint and liaise with the call center
• Set up studies in Recruitment SharePoint based on protocols for all Clinical Pharmacology sites, including screening appointments
• Produce study recruitment reports and warm calling lists
• Distribute and update the recruiting manual
• Notify the Recruitment Supervisor or designee of concerns or problems
• Coordinate necessary screening information with the screening department
• Monitor and assess advertising response and scheduled screening appointments
• Monitor recruitment progress and report to management
• Assist with maintaining subject status updates in the database
• Assist with compiling monthly management reports
• Advise call center staff and review their work for quality
• Monitor call center staff to ensure exemplary customer service and high panel fill rates
• Assist with recruitment activities for enrolling studies at each Clinical Pharmacology site, including advertisement creation
• Perform other duties as assigned

Call Center Coordinator II

Clinical Operations

• Execute and oversee local operational clinical trial activities at the country level
• Own and oversee local regulatory and financial compliance
• Deliver country-specific trial commitments and objectives, especially during study start-up
• Influence investigators, vendors, external partners, and country managers to deliver commitments
• Adhere to budget targets and payment timelines
• Address and resolve issues and develop country risk management and mitigation plans
• Manage country and site budgets and clinical research-related payments
• Reconcile payments at study close-out
• Execute and oversee country submissions and approvals for assigned protocols
• Develop local-language materials, including informed consents and translations
• Work with IRB/IEC and Regulatory Authorities on submission and approval interactions
• Manage country deliverables, timelines, and results for assigned protocols
• Contribute to local SOP development
• Collaborate with clinical operations, quality, finance, medical, regulatory, pharmacovigilance, compliance, legal, regional operations, vendors, sites, IRBs/IECs, and Regulatory Authorities
• Align country timelines with Regional Operations and oversee local vendors
• Oversee clinical and ancillary supplies, importing/exporting, supplies destruction, filing, archiving, retention, and insurance processes
• Enter and update country information in clinical, regulatory, safety, and finance systems
• Perform other duties as assigned

Clinical Operations Manager

• Respond to medical information queries, product quality complaints, and general queries received by telephone, email, fax, and other channels
• Receive, record, and report Adverse Drug Reactions within required timelines according to regulations and internal WI/SOPs
• Execute drug safety data management processes, including call intake, call dialogue documentation, peer review, and case follow-up
• Perform and support assigned activities, including tracking information and metrics, ongoing quality control of defined process steps, training, and reconciliation of data from multiple sources
• Assume responsibility for the quality of processed data
• Perform other duties as needed or assigned

Medical Contact Center Associate I

Financial Planning and Analysis

• Prepare country site budgets and study financial appendices
• Assist with negotiation of site agreement budgets and financial exhibits
• Develop Clinical Trial Agreements (CTAs) using standard templates and Contract Information Sheets
• Ensure CTAs are executed in a timely manner to meet study start-up timelines
• Liaise with legal departments regarding CTA content changes and approved agreement language
• Participate in study kick-off meetings
• Review proposed CTA language modifications and resolve compliance issues with legal departments, sites, contractors, or vendors
• Generate site budgets from approved country budgets and follow up with investigators
• Research medical procedure costs using local or global databases
• Manage CTAs, agreement changes, and related components according to legal standards and Global SOPs
• Coordinate annual template reviews with Legal and monitoring/site management leadership
• Manage the contract tracking database and reconcile discrepancies
• Post fully executed contracts in eFiliA and the Clinical Operations secure drive
• Process internal approval forms and documents for signatory compliance and annual audits
• Serve as point person among site personnel, clients, Clinical Operations, Legal Counsel, and Insurance/Management throughout negotiations
• Maintain complete and accurate documentation for internal audits
• Negotiate and review Master Services Agreements with institutions before renewal
• Support country study site budget template, parameter, and payment term building
• Execute site budget maintenance throughout the study lifecycle
• Negotiate master clinical trial agreement rate cards with globally assigned sites
• Partner with site payment departments to ensure budget and payment-term compatibility with payment systems and EDC requirements
• Partner with Study Startup, Clinical Operations, and TAU teams to improve SB&C metrics and processes
• Apply standards across projects and portfolios and support continuous improvement
• Develop TA-aligned strategies and provide budget/payment-term feedback using industry tools, data sources, and fair market value guidance
• Identify potential delays and escalate non-performance

Senior Medical Director, MD

Clinical Research Associate II, Phase I

Business Development Director II – Early Phase

Senior Business Development Director – Early Phase

Vice President, Global Therapeutic Area Leader, Oncology

Senior Clinical Data Manager – FSO

Senior Clinical Scientist – Immunology

Clinical Research Associate II, Phase I

FSP Clinical Scientist III / Medical Science Liaison

Clinical Research Associate 2

Director, Project Management – Rare Disease & Pediatrics

Call Center Coordinator II

Clinical Operations Manager

Medical Contact Center Associate I

Site Budgeting and Contracting Specialist