Additionalinformation

Additional Information

What we offer:

• We value your time so the recruitment process is as quick as 2 meetings!
• We'll prepare you to do your job at highest quality level with our extensive onboarding and mentorship program
• You'll have excellent working conditions - spacious and modern office in convenient location, and friendly, supportive team who love to hang out together
• You'll have permanent work agreement at a stable, privately owned company
• We care about our employees - aside from competitive salary, you'll have good work-life balance with flexible working hours and additional days off, life and medical insurance, sports card, lunch card
• We're constantly growing which means opportunities for personal and professional growth

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. Please provide your CV in English.

If you have any questions, don't hesitate to reach out to the recruiter at [email protected] or on Karolina Karaszewska | LinkedIn

Companydescription

Company Description

Why PSI?

Because we are not a huge corporation and people still matter here. Our managers and employees have autonomy in making decisions and creating an engaging work environment. We provide the operational freedom to make nuanced country and department-specific adjustments, adhering to our common goals and culture that unites us across six continents.

Learn more why you should join PSI here!

Jobdescription

Job Description

As a CRA at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

Hybrid work with office in Warsaw.

You will:

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions
• Prepare and participate on audits and inspections

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Experience in independent on-site monitoring in all types of visits is required
• Experience in gastroenterology TA is required
• Experience in neurology and oncology is a plus
• Full working proficiency in Polish, English and in MS Office applications
• Ability to travel and a valid driver's license

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