IQVIA

Team Lead

• Independently manage end-to-end delivery of data management services for single- and multi-service projects, ensuring quality, timelines, budget, and customer satisfaction
• Provide data management expertise and leadership to Clinical Data Management teams
• Lead project planning, execution, close-out, financial management, communications, and milestone deliverables
• Serve as Data Team Lead, Program Lead, Customer Site Manager, and/or Subject Matter Expert as needed
• Serve as primary customer contact for data management deliverables
• Manage multiple large global studies or programs and support Data Team Leads
• Manage customer negotiations, timelines, finances, processes, resources, issue escalation, and continuous process improvements
• Coordinate with Data Operations teams to ensure milestones and quality deliverables
• Train, develop, and mentor junior team members
• Independently manage data management service delivery and resolve escalated data issues
• Assign resources and create, review, and approve data management plan documents
• Implement quality management plans, identify root causes, and implement remedial actions
• Lead organizational change and service improvement initiatives
• Serve as a subject matter expert in CDM tasks or technology and as customer site lead
• Maintain internal tracking databases and systems
• Manage statements of work and budgets, review financial reports, track change orders, and support pricing discussions
• Serve as Project Manager for single-service data management projects, including financial tracking, revenue recognition, and invoicing
• Support RFP processes, including document review, pricing, and bid defense
• Lead best-practice teams, communicate lessons learned, and present at workshops
• Manage development and implementation of new technology or tools
• Present at professional conferences and/or publish articles
• Review and provide expert input on operating procedures and work instructions
• Perform other duties as directed by the functional manager

Senior Data Team Lead

Clinical Research

• Adhere to Sponsor SOPs, WIs, policies, Good Clinical Practice (GCP), and local regulatory requirements
• Serve as a subject matter expert and resource for quality and compliance standards across assigned studies
• Lead and contribute to site selection, site feasibility, site qualification visits, and site performance optimization
• Coordinate local team activities, recruitment planning, contingency and risk management, budget forecasting, and mitigation strategies
• Act as primary Sponsor contact and local operational lead for assigned complex studies
• Maintain and update trial management systems and analyze trial progress, risks, trends, and issues
• Initiate corrective and preventive actions (CAPA) when studies deviate from plans
• Develop and execute country-level recruitment strategies and contingency planning
• Manage country-level vendors, vendor performance, issue resolution, budgets, invoices, and local study supplies
• Lead local trial team meetings and facilitate Site Manager training
• Prepare and manage country- and site-specific informed consent documents
• Ensure adverse events and patient safety concerns are reported and escalated appropriately
• Maintain inspection readiness, complete trial data, and essential documents in CTMS and eTMF/IF systems
• Oversee site data quality, query resolution, operational performance, and CAPA implementation
• Manage country/local trial budgets, financial reporting, forecasting, and mitigation plans
• Coordinate IEC/HA approvals and provide guidance on regulatory requirements
• Train, mentor, and coach less experienced team members
• Lead process improvement, operational excellence, inspection readiness, and new system implementation initiatives
• Lead country-level operational planning and execution for complex, high-priority, or high-risk studies

Senior Clinical Trial Manager, Oncology

Account Manager

• Support the successful implementation of the National Immunisation Programme across NHS systems
• Work closely with stakeholders across Integrated Care Systems and Primary Care Networks
• Drive vaccine uptake
• Optimise patient identification and recall processes
• Support a COPD-focused Quality Improvement Programme
• Help healthcare professionals identify, review and optimise appropriate patient cohorts
• Influence stakeholders and deliver measurable outcomes through customer engagement and partnership working

Pharmacy Account Manager

Pharmacist

• Support practices with clinical tools and resources to manage patients with long-term conditions
• Ensure clinical services are delivered within protocols, service operating instructions, and systems
• Identify opportunities for clinical reviews at practice, PCN, or ICB level where there is clinical need
• Enhance awareness of Interface Clinical Services within primary care
• Develop long-lasting relationships with practices and local NHS organisations
• Support patients with chronic conditions in primary care settings

Clinical Pharmacist

Project Manager

• Lead and manage eCOA implementation projects from initiation through startup
• Create, track, and report on project timelines and deliverables
• Manage project budgets, scope changes, and invoice approvals
• Prepare and present project updates to internal teams and external sponsors
• Coordinate with global teams and vendors to ensure timely translations and configurations
• Run client meetings, take meeting minutes, and maintain clear communication
• Identify risks, troubleshoot issues, and negotiate out-of-scope work
• Maintain compliance with SOPs, policies, and quality standards
• Drive process improvement initiatives and contribute to proposal development
• Serve as a backup contact for internal Project Managers when needed
• Ensure accurate financial reporting, including tracking deliverables and invoicing
• Partner with other Project Managers to implement process improvements
• Communicate effectively with sponsors and clinical teams, including presenting timelines and status updates
• Support onboarding by collaborating with team members and mentoring new hires
• Occasionally travel for sponsor meetings (domestic or international, as needed)

eCOA Implementation Project Manager

Manager

• Manage licensing and electronic implementation processes of Clinical Outcome Assessments (COAs) for clinical trials.
• Serve as primary contact with external vendors and internal departments.
• Track performance of assigned COA businesses, including sales/revenue and staff allocation.
• Oversee COA licensing activities and programs from study initiation through closeout.
• Partner with study project managers and set up vendors within IQVIA systems.
• Facilitate legal reviews and approvals and ensure quality deliverables are delivered on time and within budget.
• Create, track, and report COA licensing project support timelines.
• Perform financial reporting, track deliverables, and manage invoicing.
• Monitor, manage, and communicate COA licensing expectations and activities to cross-functional project teams.
• Coordinate with project resources within and outside the organization.
• Negotiate COA licensing costs and contracts.
• Develop and maintain internal databases of COA licensing requests and project plans.
• Participate in proposal development and sales/proposal presentations.
• Meet regularly with team members regarding project tasks to ensure milestones are met.
• Ensure work complies with standard processes, policies, and procedures and meets project timeline metrics.

Manager, Licensing & Distribution

Consultant

• Support the design and delivery of patient-focused and outcomes research projects for pharmaceutical, biotechnology, and healthcare clients
• Support the design and build of technology solutions for patient-centered research, outcomes research and HEOR studies
• Conduct qualitative and quantitative research involving patients, caregivers, clinicians and other healthcare stakeholders
• Manage internal and external cross-functional stakeholders to support product development
• Create reports, presentations and workshops for client employees, management teams and other stakeholders
• Develop knowledge of consulting methodologies and the pharmaceutical market through consulting engagements and learning opportunities
• Assist with developing and writing proposals with senior support
• Attend, support and present at client meetings

Associate Consultant, Outcomes Research – HEOR / PROs

• Support practices with clinical tools and resources to manage patients with long-term conditions
• Ensure clinical services are delivered within protocols, service operating instructions and systems
• Identify opportunities for clinical reviews at individual practice, PCN or ICB level where there is clinical need
• Increase awareness of Interface Clinical Services within primary care
• Help develop long-lasting relationships with practices and local NHS organisations
• Manage own diary to enable flexible working and work in practice
• Support patients with chronic conditions in primary care settings

• Perform site monitoring visits, including selection, initiation, monitoring, and close-out visits, in accordance with contracted scope and regulatory requirements
• Work with sites to adapt, drive, and track subject recruitment plans
• Administer protocol and related study training to assigned sites
• Establish regular communication with sites to manage project expectations and issues
• Evaluate study-site quality and integrity regarding protocol conduct and regulatory adherence; escalate quality issues
• Track regulatory submissions and approvals, recruitment and enrollment, CRF completion and submission, and data-query generation and resolution
• Support the study start-up phase as needed
• Ensure site documents are available for Trial Master File filing and verify Investigator's Site File maintenance
• Create and maintain site-management and monitoring documentation, including visit reports and follow-up letters
• Collaborate with study team members to support project execution

Clinical Research Associate

• Perform site monitoring visits, including selection, initiation, monitoring and close-out visits
• Work with sites to adapt, drive and track subject recruitment plans
• Administer protocol and study training to assigned sites
• Establish regular communication with sites to manage project expectations and issues
• Evaluate study site practices for protocol quality, integrity and regulatory adherence
• Escalate quality issues as appropriate
• Track regulatory submissions and approvals, recruitment and enrollment, CRF completion and submission, and data query generation and resolution
• Support the study start-up phase where applicable
• Ensure site documents are available for Trial Master File filing
• Verify Investigator's Site File maintenance according to GCP, ICH and local regulatory requirements
• Create and maintain site management documentation, monitoring visit findings and action plans
• Submit visit reports and generate follow-up letters and required study documentation
• Collaborate with study team members to support project execution
• Support development of project subject recruitment plans on a per-site basis where applicable
• Support site financial management and retrieve invoices according to local requirements where applicable

Clinical Research Associate – Sponsor Dedicated

Supply Chain

• Interpret clinical trial protocols to create and execute an effective clinical trial supply chain solution
• Create master English label text in accordance with relevant regulatory frameworks, such as Annex 13
• Create and maintain demand forecasts and packaging plans
• Initiate packaging campaigns with assigned vendors and oversee on-time delivery
• Set up, monitor, and update study-assigned Interactive Response Technology (IRT) systems
• Create distribution plans and oversee assigned vendors executing them
• Ensure trial materials are delivered to the right place at the right time
• Track budgets to ensure efficient project execution within client-approved quotations
• Maintain 100% compliance with assigned training and apply learnings in daily practice
• Remain current on applicable GxP and regulatory requirements
• Lead client and vendor meetings concerning clinical supply chain topics or status updates
• Create a Temperature Excursion management plan
• Manage review and assessment of Temperature Excursions reported to the IQVIA Clinical Trial Supplies team
• Conduct regular risk management assessments and execute appropriate mitigations

Clinical Supply Chain Manager

• Support practices with clinical tools and resources to help manage patients with long-term conditions
• Ensure clinical services are delivered within protocols, service operating instructions, and systems
• Identify opportunities for clinical reviews at individual practice, PCN, or ICB level where there is clinical need
• Increase awareness of Interface Clinical Services within primary care
• Assist in developing long-lasting relationships with practices and local NHS organisations
• Manage own diary to enable flexible working and in-practice work
• Support patients with chronic conditions in primary care settings

Analyst

• Develop materials and services for UK HTA and HEOR project delivery, including dossier writing, early HTA scientific advice, HTA landscape reviews, literature reviews, health economic model development and adaptations, submission support, and pricing negotiation support
• Contribute to multi-country HTA and HEOR projects across different markets and product types
• Develop strategic HTA knowledge and skills, particularly in UK HTA processes and requirements
• Collaborate with internal project teams, client teams, technical consultants, Market Access, Patient-Centered Solutions, HTA Accelerator Solutions, database studies, and local teams across IQVIA’s global network
• Support HTA thought leadership through conference abstracts, posters, white papers, and guidance of interns on HTA-focused thesis topics
• Develop knowledge of global HTA and HEOR offerings to support business development opportunities
• Work flexibly across multiple projects and complete assigned tasks within core company working hours and deadlines

Analyst, Health Technology Assessment Strategy and Implementation

Clinical Data Coordinator

• Serve as Senior Data Coordinator for allocated complex studies and serve in a leadership role to a specific DM Task
• Serve as a lead DM and the main point of contact for various projects managed by the team
• Ensure all deliverables meet expected quality standards and customer expectations
• Attend study kick-off meetings and internal/sponsor audits for assigned studies
• Report on data collection quality and site issues to Data Management Team Leaders and apprise them of project status
• Interact with Clinical Data Management personnel regarding project timelines, quality data delivery and project update teleconferences
• Resolve all Data Clarification forms, clean data, send data transfers to the sponsor according to agreed specifications, and complete and appropriately archive data and study files at study close
• Mentor team members and ensure completion of required training
• Assist in developing and implementing new technology/database revisions

Senior Clinical Data Coordinator

Strategy

• Shape and lead the team and HTA offerings with senior leadership and global centres of excellence
• Manage business development and client relationships, understand strategic goals and milestones, and manage project scope
• Manage HTA project strategy and direction, particularly UK HTA processes and requirements
• Identify potential challenges to product value and develop risk mitigation strategies
• Manage project delivery teams across dossier development, UK HTA submission support, early scientific advice, HTA strategy, and strategic HTA offerings
• Contribute to multi-country and global HTA projects
• Mediate, negotiate, and solve problems within and outside project teams
• Train and identify development opportunities for junior HTA team members
• Collaborate across IQVIA technical consulting, Market Access, Patient-Centered Solutions, HTA Accelerator Solutions, database studies, and local global-network teams
• Liaise with pharmaceutical, biotechnology, and medical device clients and their affiliate teams
• Support or lead HTA thought leadership, including conference abstracts, posters, white papers, and peer-reviewed publications
• Guide interns working on HTA-focused thesis topics
• Provide line management depending on interests

Senior Data Team Lead

Senior Clinical Trial Manager, Oncology

Pharmacy Account Manager

Clinical Pharmacist

eCOA Implementation Project Manager

Manager, Licensing & Distribution

Associate Consultant, Outcomes Research – HEOR / PROs

Clinical Pharmacist

Clinical Research Associate

Clinical Research Associate – Sponsor Dedicated

Clinical Supply Chain Manager

Clinical Pharmacist

Analyst, Health Technology Assessment Strategy and Implementation

Senior Clinical Data Coordinator

Senior Global HTA Strategy Consultant