We love what we do and our business is growing continuously.

Due to the continuous growth we always need good people in different operational working areas of our company. However, our aim is to be the best CRO providing the best services to our clients. For this reason we only need the best people.

Clinical Trial Assistant (CTA) in Slovakia

GCP-Service International s.r.o. offers clinical research services throughout Europe using the latest modern technologies. We provide clients with highly professional services based on long-term cooperation, trust and personalized services for either pharmaceutical companies or manufacturers of medical devices.

We are recruiting for CTAs (Clinical Trial Assistant) based in Slovakia to work outsourced to our client, a leading pharmaceutical company, currently offering 0.5 FTE that can be increased in the future. The candidate will be responsible for completion of all administrative tasks associated with assigned clinical trials according to ICH GCP, applicable regulatory requirements and Standard Operating Procedures (SOPs).

Clinical Trial Assistant makes backup of Office Manger in case of his/her absence and vice versa.

Core responsibilities:

  • Performs administrative activities in relation with clinical trials according to Clinical Research Management, Project Managers (PMs), Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) instructions.
  • Prepares documentation for Ethics Committees and Regulatory submissions as per SOPs.
  • Distributes materials/documents to the sites as per SOPs.
  • Communicates with the site staff.
  • Acts with other agencies, organizations and groups.
  • Records received SAE reports and ensures their timely delivery to the Sponsor.
  • Participates in the organization of Investigator’s meetings.
  • Controls and proceeds clinical trial correspondence as per SOPs.
  • Maintains in-house study documentation as per SOPs.
  • Prepares study documentation for archiving.
  • Is responsible for archive facility as per SOPs.
  • Ensures proper record retention.

Qualifications needed:

  • Basic knowledge of ICH GCP guidelines and regulatory requirements.
  • Good verbal and written communication skills
  • Knowledge of office administration.
  • Very good organizational and interpersonal skills.
  • Very good in record retention, time management, decision making and customer service.
  • Flexibility.
  • Teamwork ability.
  • Fluent in English, written and verbal.
  • Good computer skills.

In case of your interest, please send us your electronic application and your CV to:

Ing Vladimira Hanusová
(Clinical Project Manager)
GCP-Service International s.r.o.
Pekarska 695/10b
155 00 Praha 5
Phone: Tel +420 918 114 498

We will be happy to give you more information during a personal meeting in our office Pekařská 10b, Praha 5.

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