Site Management Associate at PSI CRO

Warsaw, Masovian Voivodeship, Poland -

Full Time

Start Date

Immediate

Expiry Date

20 Apr, 26

Salary

0.0

Posted On

20 Jan, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Database Management, Document Management, Communication, Query Resolution, Project Coordination, Meeting Arrangement, Organizational Skills, Planning Skills, Problem-Solving Skills, Multi-Tasking, Teamwork, MS Office Proficiency, Life Sciences Knowledge, Administrative Experience, Bilingual Proficiency

Industry

Pharmaceutical Manufacturing

Description

Company 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.

Responsibilities

The Site Management Associate will maintain databases and manage documents to support clinical research projects. They will also serve as the primary communication point for investigative sites and coordinate project training.