Clinical Research Associate II

September 15

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Parexel

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Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions

10,000+

💰 Venture Round on 1990-01

Description

• Parexel FSP is looking for CRA in Poland to strengthen our clinical operations team. • Work from home and with the flexibility you want. • Our CRAs have less travel and less workload to maintain work-life balance. • We offer long-term projects, world-class technology and training tailored to your individual experience. • As a CRA, you will work independently and will be responsible for all activities required to set up and oversee a study, complete study status reports, and maintain study documentation. • You will participate in the submission of protocols, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. • You will have the opportunity to be a unique sponsor dedicated to one of the top 10 pharmaceutical companies in the world, working on oncology studies that deliver real impact.

Requirements

• Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline. • Minimum of 2 years of active independent field monitoring experience - all types of visits. • Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. • Ability to perform all clinical monitoring activities independently. • Strong interpersonal, written, and verbal communication skills within a matrixed team. • Experience working in a self-driven capacity, with a sense of urgency and limited oversight. • A client-focused approach to work and flexible attitude with respect to assignments/new learning. • The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s). • An honest and ethical work approach to promote the development of life changing treatments for patients. • Understanding of ICH GCP Compliance. • Excellent time management and social skills. • Highly motivated with a phenomenal eye for detail. • Ability to travel domestically and internationally approximately 65%-75% of working time.

Benefits

• Premium salary. • Car. • Paid holidays. • Medical care plan: Health, Dental & Vision. • Life Assurance. • Company cell phone and equipment. • Market leading PTO. • Culture of teamwork and collaboration. • People who motivate and face challenges together. • Innovative technology. • Excellent training.