IQVIA

About the Company

IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA's portfolio of solutions are powered by IQVIA Connected Intelligence(tm) to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI(tm), advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA's insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.

Listed Jobs

Company Name

IQVIA

Job Title

Candidature spontanée délégué médical (GP/SP/PHARMA) expérimenté (m/f/x)

Job Description

**Job Title** Pharmaceutical Medical Representative – Experienced **Role Summary** Engage with general practitioners, specialists, and pharmacists to promote a portfolio of pharmaceutical products. Build and maintain trusted relationships, strategically plan visits, gather customer feedback, and identify key opinion leaders to achieve sales and market‑share targets. **Expectations** - Reach or exceed assigned sales and KPI targets. - Develop long‑term, trust‑based relationships with healthcare professionals. - Deliver consistent, compliant, and evidence‑based product presentations. - Proactively identify and engage key opinion leaders and decision‑makers in the region. **Key Responsibilities** - Conduct scheduled visits to physicians and pharmacists in assigned territory. - Present and demonstrate product features, clinical data, and positioning to healthcare professionals. - Develop and execute an individualized visit plan to maximize coverage and impact. - Identify and engage key opinion leaders (KOLs) within the region. - Collect, analyze, and report product feedback and market intelligence. - Participate in team and product‑specific training, seminars, and cycle meetings. - Maintain up‑to‑date knowledge of disease states, competitive landscape, and regulatory requirements. - Ensure compliance with company policies, ethical sales practices, and relevant regulatory standards. **Required Skills** - Excellent oral and written communication in French. - Strong interpersonal and relationship‑building abilities. - Persuasive presentation and negotiation skills. - Strategic planning and analytical thinking. - Proficiency in CRM and Microsoft Office applications. - Valid driver’s license (Category B). **Required Education & Certifications** - Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or related field. - Minimum of 2–3 years’ experience as a Medical/Pharmaceutical Representative or in a comparable health‑care sales role. - Ongoing professional development in product knowledge and sales techniques.

Zaventem, Belgium

Remote

27-11-2025

Company Name

IQVIA

Job Title

Consultant Healthcare Institutions

Job Description

**Job Title** Healthcare Institution Consultant **Role Summary** Provide consulting services to hospitals and health‑care institutions, analysing current operations, identifying improvement opportunities, and designing and implementing tailored, data‑driven solutions. Manage project lifecycles, collaborate closely with clients, and motivate teams to achieve measurable operational enhancements. **Expectations** - Deliver projects on schedule and within scope. - Work independently and as part of cross‑functional teams. - Communicate findings and recommendations clearly to stakeholders. - Foster a culture of continuous improvement and evidence‑based decision making. **Key Responsibilities** - Conduct comprehensive operational analyses of hospitals. - Identify improvement opportunities and develop realistic, quantitative recommendations. - Design, pilot, and roll‑out improvement processes. - Manage project life‑cycle from initiation through delivery of results. - Build and maintain strong client relationships; serve as point of contact on‑site and from office. - Facilitate change management, including training and knowledge transfer. - Produce regular status reports, dashboards, and final deliverables. - Stay current on healthcare sector trends, regulations, and best practices. **Required Skills** - Strong analytical and problem‑solving abilities. - Data‑driven decision making and use of quantitative evidence. - Project management methodology and ability to manage budgets, timelines, and deliverables. - Motivational and change‑management skills. - Excellent verbal and written communication in English and at least one other official language of Belgium (French or Dutch). - Independent work ethic, team collaboration, and stress resilience. - Proficiency in MS Office (Excel, PowerPoint, Word). **Required Education & Certifications** - Bachelor’s or Master’s degree in Healthcare Management, Public Health, Business Administration, Health Informatics, or related field. - Professional certifications preferred (e.g., PMP, Lean Six Sigma, CPHq). - Prior consulting or project‑management experience in the healthcare sector. - Bilingual fluency (English + French or Dutch) and willingness to travel within Belgium.

Berchem, Belgium

Hybrid

30-11-2025

Company Name

IQVIA

Job Title

International Projects Director, Commercial Pharma

Job Description

**Job Title** International Projects Director, Commercial Pharma **Role Summary** Lead and manage complex, multi‑country projects and programs in the commercial sector of Pharma/MedTech. Ensure high‑quality deliverables, on‑time delivery, and adherence to budget, policy, and regulatory requirements while supervising field‑based teams and acting as the primary liaison with stakeholders. **Expectations** - 12+ years total experience, including 7+ years in project management within pharma/medtech. - Proven track record of successful execution of cross‑functional, geographically dispersed programs. - Strong leadership, communication, and decision‑making skills. **Key Responsibilities** - Plan, execute, and deliver projects/programs in alignment with scope, objectives, and quality standards. - Serve as the primary point of contact for internal and external stakeholders; maintain effective communication and reporting. - Develop comprehensive project plans, manage deliverables across all phases, and oversee project tracking systems. - Collaborate with Business Development to finalize budgets and scopes of work; manage financial performance to meet realization targets. - Identify risks and implement mitigation strategies via quality and risk management plans. - Allocate resources and ensure availability to meet project needs. - Act as key relationship manager for clients; address issues and implement solutions with senior leadership. - Participate in RFPs, feasibility assessments, and proposal presentations. - Represent project management in cross‑functional and client‑facing committees. - Manage staff in accordance with company policies, including performance management, development, and HR actions. **Required Skills** - Strategic project and program management - Leadership and team development - Stakeholder and client relationship management - Budget planning and financial performance oversight - Risk identification and mitigation - Effective communication, reporting, and presentation - Influencing, negotiation, and decision‑making - Ability to manage multiple priorities and stakeholders **Required Education & Certifications** - High school diploma or equivalent (required); higher education preferred. - Relevant certifications preferred: PMP, PRINCE2, or equivalent project management credential.

Reading, United kingdom

Hybrid

Senior

03-12-2025

Company Name

IQVIA

Job Title

Clinical Research Associate, Real World Evidence

Job Description

**Job Title:** Clinical Research Associate, Real World Evidence **Role Summary:** Support Phase 3b and Phase 4 real‑world evidence studies by conducting site monitoring visits, ensuring adherence to GCP/ICH and regulatory requirements, and managing study progress, recruitment, data quality, and documentation throughout the clinical trial lifecycle. **Expactations:** - Execute independent on‑site monitoring (minimum 6 months) across multiple protocols and sites. - Maintain high standards of protocol compliance, data integrity, and regulatory filings. - Travel to sites throughout the UK and Ireland as needed. **Key Responsibilities:** - Plan and perform initiation, monitoring, and close‑out visits per contractual scope. - Collaborate with sites to develop, drive, and track subject recruitment plans. - Deliver protocol and study training to sites; maintain regular communication streams. - Assess site practices for protocol fidelity and regulatory compliance; flag and escalated quality issues. - Track and report on submissions, approvals, recruitment, enrollment, CRF completion, and data query resolution. - Ensure proper filing of TMF/ISF documents as per GCP and local regulations. - Produce monitoring reports, follow‑up letters, and other documentation for study team and regulatory bodies. - Coordinate with study teams for operational support and issue resolution. **Required Skills:** - Independent on‑site monitoring experience (≥6 months). - Proven track record managing multiple clinical protocols across diverse sites. - Deep knowledge of GCP and ICH guidelines. - Strong communication and interpersonal skills for site interaction. - Detail‑oriented documentation and data management abilities. - Proactive problem‑solving and quality‑issue escalation capacity. - Willingness to travel to sites throughout the UK and Ireland. **Required Education & Certifications:** - Life sciences degree (pharmacy, biology, medicine, or related field) OR equivalent industry experience. ---

Reading, United kingdom

On site

03-12-2025