Clinical Trial Assistant (CTA)

SanaClis s.r.o.

Place of work
Contract type
Start date
to be agreed
Wage (gross)
1 100 - 1 200 EUR/monththe salary will be agreed based on qualification, experience and skills of an applicant

Information about the position

Job description, responsibilities and duties

You will support the Clinical Operations team with ongoing conduct of clinical studies. Including:
Provide general administrative support to the Clinical Operations Department and assistance to Project Director(s)/Manager(s) and CRAs.
Assist CRA/PM in study-related tasks (organization of travel, filing, copying, translation from/into English, supplies planning and local purchasing, archiving, etc.) as requested by CRA/PM.
Assist CRAs in preparation of clinical trial application (CTA) and its submission to ethics committees (EC) and national regulatory authorities (RA).
Help in preparation of ISFs and other study related files.
Update tracking forms and other relevant documents as requested by CRA/PM.
Assist in quality control checks of clinical trial documentation (e.g. TMF, ISF, CTA, etc.) including preparation for internal/external audits, final reconciliation and archival.
Communicate with investigators, authorities, sponsor (phone, e-mail, face to face) on behalf of CRA/PM in respect to all study related issues delegated to CTA by CRA/PM. Inform CRA/PM about the results correspondingly.

Employee perks, benefits

We are an equal opportunities employer, in terms of gender and age. We create family friendly environment offering flexible working time, babysitting, home based work. We care about work-life balance of our employees.
Other employee benefits will be specified during job interview

Information about the selection process

A successful candidate must have:
Knowledge of clinical research processes and medical terminology.
Good knowledge of ICH GCP, national Regulatory requirements.
Previous experience in CTA position or familiarity with clinical trials is a benefit.

Requirements for the employee

Candidates with education suit the position

University education (Bachelor's degree)
University education (Master's degree)
Postgraduate (Doctorate)

Educational Specialization

preferred qualification in nursing, life sciences or medical sciences

Language skills

English - Upper intermediate (B2) and Slovak - Proficiency (C2) and Hungarian - Advanced (C1) and Czech - Advanced (C1)

Other knowledge

Microsoft Outlook - advanced
Microsoft Excel - advanced
Microsoft PowerPoint - advanced
Microsoft Word - advanced

Driving licence


Personality requirements and skills

Able to overview the whole picture as well as focus on details.
Strong written and verbal communication skills to express complex ideas to study personnel. Able to work remotely in international teams. Confident in communication.
Good social and cooperation skills, able to support others.
Good time management and organization skills, able to plan and meet timelines, able to prioritize.


Brief description of the company

SanaClis is a full-service European CRO offering a comprehensive range of services for clinical trials. In additional to being a full-service CRO, SanaClis is one from very few CROs in the world who has in-house logistics capabilities. This includes QP services, customs brokerage, warehousing and distribution, and sourcing of clinical trial materials, comparators and rescue medication.

Number of employees

10-19 employees

Company address

SanaClis, s.r.o.
Staré grunty 130
841 04 Bratislava - mestská časť Karlova Ves
ID: 3740490  Dátum zverejnenia: 12.2.2020  Základná zložka mzdy (brutto): 1 100 EUR/month