Clinical Research Associate in Denmark or Sweden

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.

Parexel is currently seeking Clinical Research Associates with knowledge of Scandinavian languages to join our team in Denmark or Sweden.

Your time here

At Parexel the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRAs are accountable for using their expertise to build and maintain the site relationship and ensure theyre set up for success. As the clinical sites sole point of contact this includes addressing and resolving site issues and questions. Youll also manage site quality and delivery from site identification through to close-out.

As a CRA Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact flexibility and career development appeal to you Parexel could be your next home.

What youll do

• Leverage your expertise. Conduct qualification visits (QV) site initiation visits (SIV) monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
• Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
• Protect patients. Review the performance of the trial at designated sites ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
• Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines while also ensuring compliance with the approved standard operating procedures (SOPs) protocol/amendment(s) GCP and the applicable regulatory requirement(s).
• Ensure quality. Evaluate the quality and integrity of the reported data site efficacy and drug accountability.
• Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.

Knowledge and Experience:

• Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology
• Excellent interpersonal verbal and written communication skills in Swedish Danish or Dutch.

Education:

• Educated to degree level (biological science pharmacy or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience

Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe. As a member of our team youll 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 CRA role into line management Quality Project Leadership or a variety of other positions Parexel prides itself on career opportunities for our employees.