# Clinical Research Associate **Company**: IQVIA **Work arrangement**: hybrid **Experience**: mid **Job type**: full-time **Category**: Healthcare **Industry**: Healthcare **Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Amsterdam-Netherlands/CRA-2--Single-Sponsor-Dedicated_R1552288?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply **Canonical**: https://yubhub.co/jobs/job_f8faa66d-2af ## Description We are seeking a Clinical Research Associate to join our Clinical Functional Service Partnerships (CFSP) team in the Netherlands. As a Clinical Research Associate, you will 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. 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 escalate 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. Requirements: - Bachelor's degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or a related discipline, or equivalent combination of education and experience. - 1.5 years 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. - Preferable 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 Dutch (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 (typically 40%, depending on study needs and sponsor requirements). - A valid Class B driver's license. Benefits: - IQVIA provides a car (with private use) or a mobility allowance, fuel, insurance, maintenance, plus essential work equipment (laptop, and iPhone) - Strong focus on professional growth, with access to learning and development resources, training programs, and opportunities to continuously build clinical and leadership expertise - Home office setup support and an annual wellness reimbursement for sport and wellbeing activities - Leave policy, including annual vacation days and additional year-end leave options - Comprehensive benefits package including pension plan, multiple insurance coverages, and optional partial reimbursement of supplementary health insurance, plus social and wellbeing activities. ## Skills ### Required - GCP - ICH guidelines - clinical trials - patient safety - data integrity - protocol compliance - study quality - Dutch - English ### Nice to have - sponsor-dedicated or cFSP environment - patient recruitment - study start-up activities --- Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Amsterdam-Netherlands/CRA-2--Single-Sponsor-Dedicated_R1552288?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)