Clinical Trial Specialist / Associate Clinical Trial Manager - FSP - Remote

Parexel is recruiting for an experienced Global Clinical Trial Coordinator to support clinical study activities in oncology as a Clinical Trial Specialist. The role involves supporting multiple phases of clinical studies, ensuring compliance with GCP, managing study documentation, and overseeing site activities, all in a fully remote setting.

Location: Remote (Europe)

Responsibilities

• Support Phase 1, 2, 3 and 4 clinical studies with guidance.
• Support activities related to study/site feasibility, start-up, maintenance, and close-out.
• Manage study and site essential document review, collection, tracking, etc. from study start-up through maintenance and close-out.
• Support the Study Lead to prepare and maintain study documents and manuals.
• Study Trial Master File (TMF) oversight.
• Organize study related meetings including preparation of agenda, minute taking, and maintenance of logs.
• Lead and present at study related meetings.
• Perform site monitoring / co-monitoring visits.

Requirements

• M.S/M.A/Ph.D or B.A/B.S/nursing degree.
• At least 3 years of experience in clinical studies, 4 preferred.
• Previous site monitoring or study coordinator experience preferred.
• Working knowledge of GCP regulations and SOPs.
• Understanding of study phases and clinical development.
• Ability to work independently and in a team.
• Advanced knowledge of Word, Excel, PowerPoint.
• Knowledge of electronic systems like Veeva Vault, Smartsheet, SharePoint.
• Knowledge of database management principles.
• Strong verbal and written communication skills.
• Willingness to travel 10-20%.