IQVIA

QA Engineer

• Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures.
• Prepare and distribute reports of findings to supervisor, operations staff, management, and customers.
• Provide consultation in interpretation of regulations, guidelines, policies, and procedures.
• Support management in promotion and assessment of compliance to regulations, guidelines and corporate policies.
• Plan, schedule, conduct, report and close audit activities in any of the countries involved with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer requirements, IQVIA SOPs and project specific guidelines/instructions.
• Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers.
• Provide interpretation and consultation to project teams on regulations, guidelines, compliance status, and policies and procedures.
• Provide consultation to customers and monitors in interpretation of audit observations and formulation of corrective action plans.
• Review, approve investigations, Root Cause Analysis (RCA), Corrective Action Prevention (CAPA) and Effectiveness Check (EC) plans and track till closure for quality events arising from Audits; and from Quality Issues, Inspections or during similar QA activities as assigned.
• Evaluate policies and procedures for compliance with applicable regulations/guidelines and provide recommendations to management for continuous process improvements.
• Maintains the electronic quality management system (eQMS) and provides support in relation to the audit lifecycle.
• Lead/collaborate/support in QA initiatives/projects for quality, process improvements.
• Assist in training of new Quality Assurance staff.
• May be required to manage Quality Issues.
• May present educational programs and provide guidance to operational staff on compliance procedures.
• May perform pre-inspection visits at sites, host audits/inspections; ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections, as assigned.

Senior QA Auditor – GCP Audits

Research Analyst

• Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
• Work with sites to adapt, drive, and track subject recruitment plan
• Administer protocol and related study training to assigned sites
• Evaluate the quality and integrity of study site practices
• Manage the progress of assigned studies by tracking regulatory submissions and approvals
• Ensure copies/originals site documents are available for filing in the Trial Master File (TMF)
• Create and maintain appropriate documentation regarding site management
• Collaborate and liaise with study team members for project execution support

Clinical Research Associate 2

Recruitment

• Coordinate the operational execution of patient recruitment and retention deliverables for assigned studies, ensuring alignment with the approved recruitment strategy and study timelines.
• Manage the coordination of translations, printing, and shipping of patient‑facing and study materials across multiple countries, working with internal teams and external vendors to ensure accuracy, quality, and timely delivery.
• Prepare and compile country‑specific submission packages and ensure required materials are delivered to Regulatory teams in accordance with submission requirements and timelines.
• Maintain and track study timelines, milestones, and deliverables using Smartsheet or other designated project management tools to support on‑time delivery.
• Support project‑specific, interdepartmental, and role‑specific training activities as required to enable consistent execution of recruitment processes.
• Maintain and manage large volumes of study‑related data, ensuring accurate and timely data entry into designated tracking systems and tools in accordance with project requirements.
• Support finance‑related activities, including contributing to periodic project and financial report generation and review.
• Ensure timely uploading, maintenance, and quality control of study documentation within eTMF/Wingspan or other designated systems, in compliance with company policies and regulatory standards.
• Ensure patient recruitment deliverables are completed accurately, compliantly, and within agreed timelines to support overall study execution.
• Identify operational risks, data discrepancies, or delivery challenges and proactively communicate issues and potential mitigation actions to relevant stakeholders.
• Perform additional duties as assigned by management to support overall project and departmental objectives.

Patient Recruitment Specialist

Administration

• Provide comprehensive administrative support to management, including calendar coordination, meeting organization, and follow-up actions
• Prepare, format, maintain, and distribute documents, reports, presentations, and routine correspondence
• Organise, record, sort, and maintain files and information in line with internal standards
• Manage email and information flow, respond to inquiries, and route requests appropriately
• Coordinate travel arrangements, meetings, and appointments as required
• Operate standard office systems and tools to support daily administrative activities
• Support managers with administrative tasks across finance, planning, HR, IT, and other corporate services as needed
• Assist with data tracking, reports, and preparation of materials for leadership discussions
• Act as a coordination point between managers and internal teams, supporting clear communication and execution
• Proactively track action items, deadlines, and deliverables to ensure follow-through
• Bring structure to complex workflows by organizing information, priorities, and timelines
• Support process consistency and identify opportunities to improve administrative efficiency
• Work confidently with systems, data, and reports to ensure accuracy and transparency
• Handle sensitive and confidential information with a high level of discretion and professionalism

Administrator

Affiliate Manager

• Develop and deliver insightful, value-added commercialization strategies
• Conduct strategy sessions with clients to outline an integrated commercial launch plan
• Leverage prioritization frameworks to focus pre-commercial team effort
• Prepare analytical proof points and recommendations for launch critical success factors
• Lead senior level meetings with clients to support launch planning
• Act as principal owner of client engagements and ensure client satisfaction
• Create and elevate new business opportunities through identified value-added follow-on work
• Mentor, coach, and share subject matter expertise with others

Asset Commercialization Partner – Emerging Biopharma

Health Information Specialist

• Identify potential gaps/barriers within EHR systems at priority IDN’s & Health Systems
• Problem solve and provide solutions and resolution of EHR gaps
• Identify workflow barriers and recommend scalable solutions
• Works collaboratively with customers including end users, licensed clinicians, IT informatics team, quality EHR Manager and analyst to provide meaningful insights to enhance patient care
• Align resources to develop comprehensive plans by priority institution
• Complete workflow assessments with institutional customers to identify potential gaps in care across the patient journey
• Develop and implement comprehensive customer specific plans
• Act as matrix team Health IT Specialist subject matter expert to both internal and external stakeholders with matrix partners across account management, medical, and other cross functional partners.
• Share insights around optimizing EHR systems to address gaps in patient care including Inpatient, Outpatient, and Emergency Department

Health Information Technology Specialist

• Identify potential gaps/barriers within EHR systems at priority IDN’s & Health Systems
• Problem solve and provide solutions and resolution of EHR gaps
• Identify workflow barriers and recommend scalable solutions
• Works collaboratively with customers including end users, licensed clinicians, IT informatics team, quality EHR Manager and analyst to provide meaningful insights to enhance patient care
• Align resources to develop comprehensive plans by priority institution
• Complete workflow assessments with institutional customers to identify potential gaps in care across the patient journey
• Develop and implement comprehensive customer specific plans
• Will act as matrix team Health IT Specialist subject matter expert to both internal and external stakeholders

Compliance

• Direct, oversee and manage large, complex, regulatory projects, ensuring quality deliverables on time and within budget.
• May act as a Project Manager for a large and complex stand-alone project or programme, involving several regulatory or technical deliverables and/or region, and/or operations
• Undertakes risk analysis, management and contingency plans
• Must ensure that regulatory colleagues on the project have the tools and training needed to undertake the various tasks
• Provides strategic regulatory and/or technical consultancy on a variety of projects, internally and externally, using innovative solutions where appropriate to produce consistent results
• Ensures compliance of regulatory processes and prepares for full Regulatory Affairs Systems Audits, accountable for any subsequent action plans
• Competently manages meetings/expectations with Regulatory Agencies and/or groups within IQVIA
• May take leadership role in bid defense strategy and planning
• May act as global regulatory or technical representative in major cross-functional global initiatives and/or may lead a global regulatory/technical initiative
• May lead/chair a session on Regulatory Affairs or related topics at a conference; deliver effective presentations to a broad audience
• Responsible for making major improvements to processes and systems across functions or large departments
• Problems faced are highly complex and require solutions drawn from best practices and expertise, as well as from extensive analysis into the root cause.

Regulatory Affairs Director

• Support integration of brand into EHR systems
• Identify and address barriers affecting patient care
• Share Electronic Health Record insights to enhance patient care
• Collaborate with Account Management and medical teams
• Develop and implement customer specific plans

Product Manager

• Own day-to-day product management for Provider Solutions offerings by translating product strategy into clear execution.
• Define and drive an actionable roadmap aligned with customer value, business priorities, and measurable outcomes.
• Partner cross-functionally with engineering, data/analytics, design, and commercial leadership to deliver capabilities that enable healthcare organizations to improve decision-making and performance.
• Ensure alignment between product delivery, customer needs, and business objectives by developing clear product requirements, managing prioritization, and delivering measurable value.
• Define initiative scope and success criteria, including problem statements, target users, KPIs, and release metrics.
• Develop clear, actionable product requirements (PRDs, epics, user stories, and acceptance criteria) to enable efficient delivery.
• Collaborate with commercial, business development, and strategy teams to ensure solutions are differentiated and aligned to market needs.

Senior Product Manager, Provider

• Perform monitoring and site management work to ensure proper conduct of study protocols.
• Conduct site monitoring visits in accordance with contracted scope of work and Good Clinical Practice.
• Collaborate with sites to drive subject recruitment plans.
• Administer protocol training and establish lines of communication with sites.
• Evaluate the quality and integrity of study site practices.
• Track regulatory submissions and approvals, enrollment, and data query resolutions.
• Ensure site documents compliance with GCP and regulatory requirements.
• Create and maintain documentation regarding site management and monitoring visit findings.
• Liaise with study team members for project support.

Senior Clinical Research Associate, Sponsor Dedicated

Principal

• Serve as the primary owner of client engagements
• Deliver engagements that create significant and lasting impact for clients
• Collaborate with leaders to identify emerging industry needs and help translate them into scalable commercial offerings
• Mentor and coach colleagues

Principal – Custom Market Research Consulting Services

Inside Sales

• Identify, research, and qualify new sales opportunities within assigned Emerging Biopharma and Pre-Commercial target accounts.
• Conduct proactive outbound outreach through phone, email, digital sales tools, and CRM-supported campaigns.
• Engage prospects in discovery conversations to understand business priorities, buying needs, timelines, and fit for IQVIA solutions.
• Monitor account, pipeline, funding, clinical, and market signals to inform targeted outreach and sales prioritization.
• Partner with Business Development, Account Management, Marketing, and Go-To-Market teams to support account planning and lead conversion.
• Maintain accurate CRM documentation of activities, contacts, account intelligence, opportunity status, and follow-up actions.

Account Manager – Inside Sales

Solutions Engineer

• Design analytics and execute them
• Provide business consulting and project management
• Synthesize complex data into actionable results
• Assist in developing detailed documentation and specifications

Senior Consultant, Commercial Solutions – Analytic Services

Data Analyst

• Ensuring data integrity and high‑quality outputs across data sources
• Support quality control processes and contribute to quality assurance for data offerings
• Perform standard data quality checks and identify trends or patterns using statistical techniques
• Evaluate business data to understand characteristics and ensure alignment with local market rules
• Analyse existing processes and suggest opportunities for improvement
• Document procedures and share knowledge to support team consistency
• Assist in resolving data exceptions and collaborate with internal teams to address client‑related queries
• Provide support to clients and business initiatives when required
• Maintain and track KPIs to monitor performance and ensure operational accuracy

Senior QA Auditor – GCP Audits

Clinical Research Associate 2

Patient Recruitment Specialist

Administrator

Asset Commercialization Partner – Emerging Biopharma

Health Information Technology Specialist

Health Information Technology Specialist

Regulatory Affairs Director

Health Information Technology Specialist

Senior Product Manager, Provider

Senior Clinical Research Associate, Sponsor Dedicated

Principal – Custom Market Research Consulting Services

Account Manager – Inside Sales

Senior Consultant, Commercial Solutions – Analytic Services

Data Analytics Analyst – SAS