Site Management Associate

Psi CRO; Województwo mazowieckie; On-site; PLN 42,000 - 56,000; Full time

Benefits offered by this job

Flexible hours

Lunch card

Life and medical insurance

Sports card

Onboarding program

Permanent contract

Job summary

Psi CRO is seeking an administrative support specialist to back clinical research projects. You will maintain databases and documents, serve as a primary contact for investigative sites and internal teams, and coordinate site queries and trainings.

You will also assist with meeting logistics and handle communications efficiently. Required is a Life Sciences degree, proficiency in Polish and English, and strong MS Office skills.

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 MS Office applications (Word, Excel, PowerPoint).
• Excellent organisational, planning, and problem-solving skills.
• Ability to multi-task in a fast-paced, team-oriented environment.

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.
• Assist with meeting arrangements, including preparation of draft agendas and minutes.
• Handle incoming correspondence and calls efficiently.

Skills

Polish language

English language

Organisational skills

Planning skills

Problem-solving

Multi-tasking

Education

Life Sciences degree

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.

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.

• 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

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.