Pharmaceutical Industry Professional Career Opportunity

3 days ago

Stockholm, Stockholm, Sweden TN Sweden Full time

Parexel is seeking a Clinical Research Associate to join their team in Denmark or Sweden.

The CRA role offers the opportunity to develop and demonstrate clinical research expertise.

As a CRA, you will be accountable for using your expertise to build and maintain site relationships and ensure they're set up for success.

You'll manage site quality and delivery from site identification through to close-out.

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.

  • 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 the 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.
Key Responsibilities:

Conduct site visits and generate visit/contact reports.

Build and maintain site relationships.

Manage site quality and delivery from site identification through to close-out.

Requirements:

Experience in site management or clinical research.

Excellent communication skills in Swedish, Danish or Dutch.

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