Clinical Project Coordinator (Temporary Contract)

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Requirements:

• Bachelor's Degree or equivalent experience
• Experience in a clinical research setting, ICH and GCP
• Excellent interpersonal, verbal and, written communication skills
• Ability to manage multiple projects and tight deadlines
• Working knowledge of the key elements of clinical trial operations
• Experience in Pharma/Biotech, CRO and/or academic research is essential

Responsibilities:

• Supports members of the Clinical Operations and Therapist Training team in the planning and conduct of cross-functional clinical research projects
• Provides day-to-day operational support for all Compass Pathways clinical trials
• Liaises with clinical trial sites to develop and implement creative solutions to address recruitment barriers/challenges
• Works closely with external collaborators, including CROs and clinical vendors, to provide robust support to clinical trial sites
• Monitors project deliverables and updates relevant stakeholders or team members on project progress, where appropriate