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Do you have quality/compliance background?

Are you interested in the dynamic clinical research industry?

We are currently looking to attract an Associate Compliance Specialist, based from home, in Czech Republic.

In this role you will be responsible for supporting and executing quality and compliance processes across the dedicated research sites in EMEA region.

You will also facilitate the tracking and reporting of compliance activities and tasks as well as maintain tools and materials, offering expertise to advance the vision of the department.

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Key roles and responsibilities of the Associate Compliance Specialist are as follows –

  • Assists staff in researching issues, tracking metrics, and maintaining reports and documentation related to quality and compliance activities and tasks
  • Facilitates quality and compliance processes and ensures appropriate execution and completion
  • Provides input into various initiatives and supports process/quality improvement projects on behalf of the department
  • Communicates with representatives within the department to ensure quality and timelines are maintained with respect to compliance activities (e.g., client audits, CAPA, Vendor selection and/or procedural documents)

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

  • Ideally educated to degree level, in a relevant qualification e.g. Science, with a background of working in a compliance/quality orientated position
  • Research experience and strong Site Operations experience would be preferable but experience of working in a highly regulated, quality focussed environment will still be considered
  • Strong oral and written communication skills
  • Solid organizational and time management skills
  • Effective problem-solving skills
  • Strong attention to detail
  • Ability to work independently as required
  • Ability to multitask and prioritize competing demands/workload
  • Fluent English
  • Proven adaptability

     

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 job in a multinational company; open and friendly organizational culture; opportunity for training and professional development in the area 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.