Clinical Research Associate (Fsp) - Poland

Do you know why we are one of only three CROs to have received the Leadership Award for 11 consecutive years? Because we appreciate our team, whose dedication and commitment to excellence is reflected in this award, and we work with heart, keeping the patient at the center of everything we do.

Join our team and develop your career with us by contributing your personal and professional talents and skills. Together we will continue to do things that matter to people.

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.

We’ll Expect You To Have

• Ability to travel domestically and internationally approximately 65%-75% of working time. Expected travelling ~2-3 days/week
• Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline.
• An honest and ethical work approach to promote the development of life changing treatments for patients.
• Minimum of 2 years of active independent field monitoring experience - all types of visits.
• Strong interpersonal, written, and verbal communication skills within a matrixed team.
• Highly motivated with a phenomenal eye for detail.
• 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).
• Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
• A client-focused approach to work and flexible attitude with respect to assignments/new learning.
• Excellent time management and social skills
• Current driver’s license required
• Understanding of ICH GCP Compliance.
• Ability to perform all clinical monitoring activities independently.
• Experience working in a self-driven capacity, with a sense of urgency and limited oversight.

Benefits Of Working With Parexel FSP

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

Send me your updated resume to [email protected] for an immediate interview.