Clinical Research Associate I - Sponsor dedicated - Netherlands - Home based (m/w/d)

IQVIA Inc; Amsterdam; Híbrido; EUR 45.000 - 65.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Company car or mobility allowance

Laptop and iPhone provided

Wellness reimbursement

Descripción de la vacante

IQVIA Netherlands is seeking a motivated Clinical Research Associate I to join our sponsor-dedicated CFSP model. You will work across innovative studies, build relationships with leading pharma partners, and grow through structured training and global career pathways.

The role emphasizes on-site monitoring in the Netherlands, with travel up to 40-60%. You will participate in start-up, maintenance, and site close-out activities, and support data integrity and patient safety across therapeutic

Formación

• University degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or related discipline.

Responsabilidades

• Conduct site qualification, initiation, monitoring, and close-out visits per study protocol and GCP/ICH.
• Ensure patient safety, data integrity, protocol compliance, and study quality at sites.
• Maintain relationships with investigators and site personnel, providing guidance and support.
• Monitor study progress including regulatory docs, patient recruitment, data queries, and site performance metrics.
• Collaborate with sites to optimize recruitment and retention strategies.
• Maintain inspection-ready documentation (ISF, TMF, monitoring reports).
• Identify and elevate risks, issues, and quality concerns; drive timely resolution.
• Partner with cross-functional teams to support project objectives.
• Mentor junior team members through coaching and co-monitoring.
• Contribute to start-up, maintenance, close-out, and site financial activities.

Conocimientos

GCP knowledge

ICH guidelines

Regulatory compliance

Communication skills

Stakeholder management

Independent working

Travel readiness

Educación

Life Sciences / Health Sciences degree

Nursing / Pharmacy background

Descripción del empleo

Why Join Clinical Functional Service Partnerships (CFSP)? At IQVIA, our Clinical Functional Service Partnership (CFSP) model gives you the best of both worlds: the variety and sponsor-level exposure of working as an embedded member of a leading pharmaceutical or biotechnology team, backed by the stability, global infrastructure, and career support of IQVIA. You'll develop deep, specialist expertise on a dedicated program, with the flexibility to expand across sponsors and therapeutic areas as your career progresses - and the security of a long-term IQVIA career even as individual programs evolve. Through our long-standing partnerships with the world's leading pharmaceutical and biotechnology companies, you'll contribute to clinical research programs that bring innovative treatments to patients worldwide, working across all phases of development and a broad range of therapeutic areas, within a culture that supports flexibility, continuous learning, and wellbeing.

IQVIA Netherlands are currently seeking a motivated Clinical Research Associate I practitioner to join our unique and dynamic Sponsor dedicated model. This is a role based in the Netherlands Build Your Future with IQVIA At IQVIA, you'll apply your clinical research expertise to drive meaningful outcomes for patients and sponsors around the world. As a Clinical Research Associate, you'll work across innovative studies and therapeutic areas, build your reputation with leading pharmaceutical and biotechnology partners, and grow your skills through structured training, mentorship, and genuine global career pathways.

Key responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols, GCP, ICH guidelines, and applicable regulatory requirements.
• Ensure investigational sites maintain high standards of patient safety, data integrity, protocol compliance, and study quality.
• Build and maintain effective relationships with investigators and site personnel, providing ongoing guidance, training, and support throughout the study lifecycle.
• Monitor study progress, including regulatory documentation, patient recruitment and enrollment, data query resolution, and site performance metrics.
• Collaborate with sites to implement and optimize patient recruitment and retention strategies to support study timelines.
• Maintain accurate, complete, and inspection-ready study documentation, including Investigator Site Files (ISF), Trial Master Files (TMF), monitoring reports, and follow-up communications.
• Identify, assess, and appropriately elevate study risks, site issues, and quality concerns while driving timely resolution.
• Partner closely with cross-functional study teams to support successful study execution and delivery of project objectives.
• Mentor and support junior clinical team members through coaching, training, and co-monitoring activities, as applicable.
• Contribute to continuous improvement initiatives and support study start-up, maintenance, close-out, and site financial activities as required.

Your Profile

• University degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or a related discipline, or equivalent combination of education and experience.
• Minimum 6 months on-site monitoring experience of clinical trials within a CRO, pharmaceutical, biotechnology, or healthcare environment.
• Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements.
• Preferrable experience in a sponsor-dedicated or cFSP environment.
• Knowledge of patient recruitment and study start-up activities is preferred.
• Excellent communication, organizational, and stakeholder management skills.
• Fluent written and verbal communication skills in local language (minimum C1 level), along with a strong command of English.
• Ability to work independently, manage multiple priorities, and collaborate effectively within cross-functional teams.
• Willingness to travel within the assigned region (up to 40-60% of working time).
• A valid Class B driver's license.

What we offer

• Choice of a company car (eligible for private use) or a flexible mobility allowance, fully covering fuel, insurance, and maintenance.
• Premium technology bundle to support your daily operations, including a laptop and an iPhone.
• Strong focus on career advancement, featuring dedicated training programs, learning resources, and pathways to build clinical or leadership expertise.
• Home office setup support, alongside an annual wellness reimbursement to fund your sports and wellbeing activities.
• Comprehensive time-off policy, including competitive annual vacation days and flexible year-end leave options.
• Premium benefits package featuring a robust pension plan, multiple corporate insurance coverages, and social activities.
• Optional partial reimbursement for supplementary health insurance policies to support your healthcare needs.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.