Clinical Trial Specialist
Révisions:
2
Chronologie:
14
Prix:
350
The Core Plan is designed for clients who need quick, reliable, and professional support with essential clinical trial tasks. Whether you're preparing documents, reviewing trial materials, or seeking guidance on basic research processes, this plan provides focused assistance to help you stay compliant and organised. It is ideal for individuals, new research teams, or small organisations looking for clear direction without requiring in-depth project involvement.
Plan Details:
Review of existing clinical trial documents (protocols, CRFs, site logs, screening logs, consent forms, visit schedules, etc.)
Identification of errors, inconsistencies, and areas needing improvement
High-level recommendations for GCP-compliant practices
Clarification of trial processes (recruitment workflow, visit schedules, data entry, binders, etc.)
Assistance with simple administrative or documentation-related tasks
Basic guidance on regulatory expectations and ethics requirements
Support in organising essential study documents (site file/TMF basics)
Email-based communication for feedback and deliverables
1 revision included
Deliverables:
Corrected/improved versions of submitted documents
Summary of findings and recommended improvements
Practical step-by-step suggestions you can apply immediately
Delivery within the agreed timeline
Wassy
Localisation:
United Kingdom
Langue:
English, French
Niveau:
10 years+
⭐
Note moyenne
Révisions:
2
Chronologie (Jours):
14
Prix: à partir de $
350
The Core Plan is designed for clients who need quick, reliable, and professional support with essential clinical trial tasks. Whether you're preparing documents, reviewing trial materials, or seeking guidance on basic research processes, this plan provides focused assistance to help you stay compliant and organised. It is ideal for individuals, new research teams, or small organisations looking for clear direction without requiring in-depth project involvement.
Plan Details:
Review of existing clinical trial documents (protocols, CRFs, site logs, screening logs, consent forms, visit schedules, etc.)
Identification of errors, inconsistencies, and areas needing improvement
High-level recommendations for GCP-compliant practices
Clarification of trial processes (recruitment workflow, visit schedules, data entry, binders, etc.)
Assistance with simple administrative or documentation-related tasks
Basic guidance on regulatory expectations and ethics requirements
Support in organising essential study documents (site file/TMF basics)
Email-based communication for feedback and deliverables
1 revision included
Deliverables:
Corrected/improved versions of submitted documents
Summary of findings and recommended improvements
Practical step-by-step suggestions you can apply immediately
Delivery within the agreed timeline
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