Site Management Associate

Psi CRO

Warszawa

On-site

PLN 52,000 - 80,000

Full time

2 days ago
Be an early applicant
Application generator

A complete application in a minute — tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Flexible working hours
On-site office in Warsaw
Life and medical insurance
Sports card
Lunch card

Job summary

Psi CRO is seeking an organised administrative professional to support clinical research projects in Warsaw. You will manage databases and documents, and act as the communication hub between investigative sites and internal teams.

Responsibilities include coordinating queries, training, and system access, as well as arranging meetings and handling correspondence. A life sciences degree and strong Polish/English skills are required.

Qualifications

  • College/University Degree in Life Sciences is required.
  • Proficiency in Polish and English.
  • Excellent organizational, 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 proficiency
English proficiency
Organizational skills
Planning
Problem solving
Team player

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 than 3000 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 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.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Clinical Trial Site Relationship Coordinator
Clinical Trial Site Relationship Coordinator

Medpace • Warszawa

On-site
PLN 120,000 - 180,000
Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
+3
Clinical Research Associate II
Clinical Research Associate II

SmartRecruiters, Inc. • Warszawa

Hybrid
PLN 60,000 - 90,000
Life insurance
Medical insurance
Sports card
+1
Senior Clinical Data Manager (all genders)
Senior Clinical Data Manager (all genders)

Merck Healthcare • Warszawa

On-site
PLN 240,000 - 420,000
Private medical care
Life insurance
Sports card
+6
Clinical Trials Assistant, Single Sponsor dedicated, office-based in Warsaw, Poland
Clinical Trials Assistant, Single Sponsor dedicated, office-based in Warsaw, Poland

IQVIA • Warszawa

On-site
PLN 68,000 - 191,000
Occasional home-office possible
Associate Director Clinical Data Manager (all genders)
Associate Director Clinical Data Manager (all genders)

Merck Healthcare • Warszawa

On-site
PLN 320,000 - 520,000
Health and well-being programs
Career development opportunities
Flexible work options
CRA II
CRA II

Fortrea • Warszawa

On-site
PLN 90,000 - 120,000
Clinical Trial Liaison - Poland
Clinical Trial Liaison - Poland

Syneos Health Commercial Solutions • Warszawa

On-site
PLN 120,000 - 160,000
CRA II
CRA II

Warman O'Brien • Polska

Hybrid
PLN 67,000 - 100,000
Company car or car allowance
Structured onboarding programme
Ongoing support and development
Clinical Site Operations Associate: Growth & Training
Clinical Site Operations Associate: Growth & Training

Psi CRO • Warszawa

On-site
PLN 52,000 - 80,000
Flexible working hours
On-site office in Warsaw
Life and medical insurance
+2
Freelance - Medical Customer Service Representative - Poland (Polish)
Freelance - Medical Customer Service Representative - Poland (Polish)

Clariness • Poland

On-site
PLN 45,000 - 89,000