Clinical Data Coordinator

SanaClis s.r.o.

Place of work
Prague, Czechia
Contract type
plný úvazek
Start date
Wage (gross)
36 000 Kč/monththe final salary will be based on mutual agreement and will reflect experience and qualification of a job candidate

Information about the position

Job description, responsibilities and duties

We are looking for a new colleague on the position of Clinical Data Coordinator in our ongoing and future Clinical Trials.
The Clinical Data Coordinator performs the data management of complex research protocols using electronic systems and data capture software.

Job responsibilities include:

- Manage all aspects of the clinical trial data management process from study start-up to database lock for SanaClis clinical trials
- Review clinical trial data in accordance with standardized data management processes (SOPs) to identify erroneous and missing data.
- Generate, resolve and track queries to address problematic data identified during data review activities.
- Assist with the development of Data Management Plan; assist in the creation of eCRF completion guideline.
- With assistance, prepare, maintain and /or review draft and final eCRF specifications and edit check specifications for assigned projects to ensure quality and consistency.
- Assist in the development and testing of data management system edit checks and special listings/procedures used as tools for the data review and discrepancy management activities.
- Perform UAT for database and test according to UAT Plan
- Ensure that all medical coding is performed on an ongoing basis throughout the life cycle of the program and at the end prior to database lock.
- Create and maintain electronic and manual edit check specifications for studies.
- Review literature and research technologies/procedures for improving DM practices.

Employee perks, benefits

will be specified during the job interview

Information about the selection process

The communication language in our company is English, so we expect you would be fluent speaker. Knowledge of other languages is considered an advantage.

We expect you would have at least basic knowledge of Clinical trial industry and ICH GCP.

Requirements for the employee

Candidates with education suit the position

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

Vzdělání v oboru

life science, computer science, bioinformatics, or similar...

Language skills

English - Advanced (C1)

Other knowledge

Microsoft Office - advanced

Number of years of experience

clinical trials, data management, or other relevant

Personality requirements and skills

You should demonstrate the ability to build and maintain effective relationships with others and establish collaborative partnerships with internal and external stakeholders.
We expect you to be results-oriented; able to set and meet short-term and long-term goals and manage multiple tasks with high attention to details and logical thinking.


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.

Company address

SanaClis s.r.o.
Stare Grunty 130
84104 Bratislava
ID: 3978046  Datum zveřejnění: 28.9.2020  Spodní hranice mzdy (brutto): 36 000 Kč/month