Senior Clinical Trial Associate (Site Intelligence Specialist) - French Speaking - UK - FSP

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's 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 we're committed to making a difference.

Parexel FSP has an exciting opportunity for a Senior Clinical Trial Associate - (Site Intelligence Specialist - SIS) to join our team in the UK. Other European locations such as France would also be suitable.

The successful candidate must have both fluent English language/written skills and advanced/fluency in French. German, Hungarian or Bulgarian language skills would also be advantageous.

Job Summary:

The successful candidate will act as a supportive team member for Site Intelligence and Site Selection. Performing tasks for multiple Site Intelligence and Feasibility projects, they will contribute to executing Site Feasibility plans and presenting the data to colleagues.

Key Accountabilities:

• Supports the Site Intelligence Lead to ensure knowledge of the goals, scope and requirements of the Site Feasibility project and ensure that high quality results are delivered.
• Participates in the Site Intelligence by reviewing internal and external intelligence on performance and quality metrics and performing literature research to identify investigators to build the database. Collects information supporting the definition of the ideal site for a study.
• Upon request from Site Intelligence Lead, provides country specific data (site contact, site recommendations) generated through collecting and interpreting feasibility data.
• Interacts with internal and external personnel to coordinate the collection of site feasibility data and contributes to the development and maintenance of the Investigator/Site Networks database to build a comprehensive list of investigational sites across all therapeutic areas per country.
• Maintains, verifies, processes, and makes updates to Client systems (including Registry), spreadsheets/documents as needed.
• Promotes a continuous improvement culture to streamline appropriate processes for maximum efficiency and productivity.
• Maintains effective relationships with other platform lines, Business Units/Research Units, and enabling lines that facilitates effective portfolio delivery.

Skills and Experience:

• Fluency/advanced working proficiency in both English and French is essential. Fluent/advanced German, Hungarian or Bulgarian language skills are also preferable.
• Demonstrated effectiveness working with multiple functions in a professional manner required.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, database applications).
• Strong presentation skills, interpersonal skills, as well as a team-oriented approach.
• Excellent verbal, written, communication and time management skills.
• Ability to multitask under tight deadlines on several projects with specific and unique requirements, while providing attention to detail and high-quality work.
• Ability to be flexible, adapt to change, work independently, as well as work as part of a team in a matrix environment.
• Demonstrated success/results in prior roles including matrix organization.

Education:

• Bachelor of Science/equivalent and 2 years' experience.

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