Browse Careers

Do you have quality/compliance background?

Are you interested in the dynamic clinical research industry?

We are currently looking to attract a QA Coordinator, based from home, in Czech Republic.

In this role you will specialise in working with MasterControl QMS and will be responsible for providing overall support to, and coordination of activities for, assigned Global Quality and Compliance (GQC) functional areas. You will prepare and maintain various records, trackers and files related to GQC activities. As a QA Coordinator you will observe and assist with relevant GQC functional area tasks, which may include internal audits, client audits, risk assessments and other activities.


Key roles and responsibilities of the QA Coordinator are as follows –

  • Oversees the creation, edit and/or retirement of user account in applicable Quality Management System
  • Partners with the QA team on other quality tasks, including but not limited to, resolution of non-conformances or CAPA support
  • Provides coordination and administrative support to management and professional staff within the applicable GQC functional area
  • Maintains files, runs reports and tracks activities for the group
  • May observe and assist with core GQC activities – internal audit conduct; client audit hosting; vendor risk assessments; etc.
  • Performs GQC functional area support for administrative functions such as procedural document deviations, CV management, intranet gatekeeping and other similar functions.

To be considered for this exciting opportunity you will need the following skills and experience -

  • Familiarity with GxP and appropriate regional clinical research regulations and guidelines
  • Experience with quality management system administration, ideally in MasterControl and in GCP environment
  • Ability to effectively work in dynamic environment
  • Strong attention to detail and accuracy
  • Ability to prioritize, multi-task responsibilities and monitor quality of own work
  • Ability to recognize when issues require escalation within the team
  • Ability to work to high standards of ethics
  • Ability to deal effectively with pressure
  • Ability to be proactive and committed to developing personal skills, knowledge and behaviours
  • Good communication skills, organizational skills and ability to work well with others
  • Computer Skills: Microsoft Word, Excel and Power Point and Internet applications
  • Good English language skills


Interested? Great, please apply ASAP as we may close the advert earlier than the expiry date.

AES is an Affirmative Action and Equal Opportunity Employer.

Competitive salary and benefits; Interesting and stable job in a multinational company; open and friendly organizational culture; opportunities for professional development in the field of clinical trials.

Accelerated Enrollment Solutions (AES) is a business unit of PPD that offers both sponsors and contract research organizations best-in-class clinical trial research site and patient enrollment solutions, with tiered offerings combining the expertise, as needed, of industry leaders PPD, Synexus, Acurian and Optimal Research.

Our success is based on a simple, but crucial, principle. We place the patient at the heart of everything we do. Synexus is a world class Site Network Organisation with global expertise spanning patient recruitment, trial planning, management and patient retention.

We recruit and retain more engaged patients, at fewer sites, and in less time than traditional centres, enhancing the quality and efficiency of our customers’ drug development programmes.