Site Management Associate

PSI CRO; Warszawa; On-site; PLN 120,000 - 180,000; Full time

Job summary

A leading clinical research organization in Warsaw is seeking a support professional to assist with clinical research projects. Responsibilities include maintaining databases, serving as a communication point, and coordinating project training. Ideal candidates will have a degree in Life Sciences, proficiency in Polish and English, and strong organizational skills. The position offers competitive salary, flexible hours, and professional development opportunities.

Benefits

Competitive salary

Flexible working hours

Life and medical insurance

Sports card

Lunch card

Professional development opportunities

Qualifications

• Prior administrative experience in Clinical Research / CRO environment preferred.
• Full working proficiency in Polish and English required.
• Excellent organisational, planning, and problem-solving skills are essential.

Responsibilities

• Maintain databases, tracking systems, and manage large volumes of documents.
• Serve as the primary communication point for investigative sites and internal departments.
• Coordinate site-specific query resolution, project training, and system access for site teams.

Skills

Organisational skills

Problem-solving skills

Multi-tasking

Communication in Polish

Communication in English

Education

College/University Degree (Life Sciences)

Tools

MS Office

Job description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

Join our international team as a key support for clinical research projects. Your responsibilities will include:

• Maintain databases, tracking systems, and manage large volumes of documents
• Serve as the primary communication point for investigative sites and internal departments
• Coordinate site-specific query resolution, project training, and system access for site teams
• Assist with meeting arrangements, including preparation of draft agendas and minutes
• Handle incoming correspondence and calls efficiently

You will streamline communication, maintain systems, and manage documents & information to support the success of our clinical research projects.

Qualifications

• College/University Degree (Life Sciences)
• Prior administrative experience in Clinical Research / CRO environment is preferred
• Full working proficiency in Polish and English
• Proficiency in standard MS Office applications
• Excellent organisational, planning, and problem-solving skills
• Ability to multi-task and work effectively in a fast-paced, team-oriented environment

Additional Information

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 havepermanent 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 meansopportunities 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.