PSI CRO AG
1001 - 5000 employees
Founded 1996
⚕️ Healthcare Insurance
💊 Pharmaceuticals
🔬 Science
Healthcare Insurance • Pharmaceuticals • Science
PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.
Senior Clinical Research Associate
🕒 May 29
🗣️🇳🇱 Dutch Required
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PSI CRO AG
1001 - 5000 employees
Founded 1996
⚕️ Healthcare Insurance
💊 Pharmaceuticals
🔬 Science
Healthcare Insurance • Pharmaceuticals • Science
PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.
📋 Description
• As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. • You will build and maintain relationships with clinical sites and investigators. • Your focus will be on subjects’ rights, safety and well-being and quality of data compliance. • Responsibilities will include conducting and reporting all types of onsite monitoring visits, driving the study startup phase, performing CRF reviews, source document verification and query resolution.
🎯 Requirements
• BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience • Independent on-site monitoring experience in the Netherlands • Demonstrable experience in all types of monitoring visits in Phase II and/or III • Strong written and verbal communication skills • Fluency in Dutch and English • Experience supporting Oncology studies is beneficial, but not essential • Advanced knowledge of MS Office • Full and clean driver's license, and the ability to travel • Communication, collaboration, and problem-solving skills are essential • Ability to multitask and work in a dynamic team environment
🏖️ Benefits
• Make the right call and take your career to a whole new level. • Join the company that focuses on its people and invests in their professional development and success. • Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. • We will guide and support you with information, making your experience as smooth as possible.
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