Details :

• Full-time contract position
• ASAP start for minimum 12 month contract
• Flexible working 3 days from home
• Competitive daily rate of pay
• Global pharma company

Specific Responsibilities:

• The position entails work under general supervision for routine tasks and with detailed instructions on new assignments.
• Primary responsibilities include: 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.

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.