My client are a global biopharmaceutical company based in West London.

They are seeking Clinical Project Associate to join their Oncology team

This is a hybrid role - 12-18 month contract

Primary responsibilities

• Tracking and preparing study-specific information utilizing databases, spreadsheets, and other tools.
• Coordinating and filing to the Trial Master File, both paper and electronic systems to ensure documents are filed and tracked in a complete and timely manner
• Working with the different members of the study management team as necessary to resolve study related administrative issues
• Serves as Clinical Trial Management Associate back up providing verbal and written communication with study personnel if appropriate.
• Under close supervision reviews and participates in the quality assurance of data or documents.
• Arranges meeting logistics.
• Drafts meeting agendas and prepares meeting minutes
• Interacts with other departments, as directed, to complete assigned tasks

Knowledge, Experience & Skills

BSc in a relevant scientific discipline preferred but not required.
* Excellent verbal and written communication skills and interpersonal skills are required.
* Must be familiar with Word, PowerPoint, and Excel.
* Knowledge of FDA and or EU Regulations, ICH Guidelines, GCP, and/or familiarity with standard clinical operating procedures is a plus.
* Must be able to work both independently and as part of a team.
* Prior experience at CPA level could be useful but not a must

Parkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.