Quality Specialist

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability.

Due to a growing portfolio, we are currently looking for a Quality Specialist to be based in Czech Republic with flexible working hours.

Your time here

At Parexel, the Quality Specialist assumes the lead (with support of LM or Mentor) of Quality oversight responsibility and partners with operational delivery teams focusing on first-time quality, robust risk and issue management and maintaining an inspection-ready state.  Provides quality expertise to support operations, leadership and clients enabling the safeguarding and maintenance of patient safety, data integrity and regulatory compliance.

The Quality Specialist focuses on PV activities, is assigned to projects and collaborates closely with the broader PQRM groups and other quality teams.

Skills:Good interpersonal, verbal and written communication skills including effective listening, facilitating group discussions, influencing without authority and providing appropriate feedbackDeveloping analytical skills focusing on identifying potential and real issues, investigating root causes, brainstorming and imagining alternatives and assessing the effectiveness of actionsAbility to develop professional, collaborative relationships both internally and with the clientDeveloping skill in interpreting, synthesizing, inferring, evaluating and extracting pertinent data to identify areas of risk, trends and aggregated issues Adaptable to changing environments, able to think quickly, able to deal with ambiguity and learn new tasks applying routine knowledgeAbility to plan, organize, prioritize and manage workload with LM guidance, keeping the patient and client at the focus Quality oriented with an attention to detail, taking initiative, ownership and accountability for deliverablesDeveloping the ability to manage the complexity of a matrix environment while valuing the importance of teamworkAbility to travel 10% -15%

Knowledge and Experience: 2+ years’ experience in clinical researchQuality and Risk Management experience is desiredKnowledge of ICH-GxP principles and clinical trial or non-clinical trial regulations as applicableEnglish proficiency (written and oral)

Education:Bachelor’s Degree or other relevant experience required. Life-science or other health-related discipline preferred

A little about us:

Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe. As a member of our team, you’ll get to know your coworkers on a personal level. Have a question? A clinical research leader, project team member, technology “super user” or collaborator are a phone call away.

Our clinical research teams meet regularly to have discussions in an open environment, allowing our team members to share their expertise and promote learning within the team. Management supports and encourages career growth through consistent performance discussions and evaluations. Whether your interest is to progress into a more senior level role, into line management, Quality, Project Leadership or a variety of other positions, Parexel prides itself on career opportunities for our employees

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