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Clinical Trial Specialist
Wassy
Location:
United Kingdom
Language:
English, Français
Level:
10 years+
⭐
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With over 15 years of experience in clinical research in the UK, I have built a strong and diverse career progressing from Clinical Trials Coordinator to Senior Clinical Trials Manager. My journey has allowed me to gain deep expertise in trial operations, team leadership, and the delivery of high-quality, compliant research.
I began my career coordinating clinical trials, where I developed solid skills in logistics, regulatory compliance, and communication across multidisciplinary teams. Moving into data management strengthened my analytical abilities and attention to detail, ensuring the accuracy and integrity of trial data. As a clinical researcher, I contributed to study design and implementation, deepening my scientific and clinical understanding. In my most recent role as Senior Clinical Trials Manager, I have led cross-functional teams, managed complex portfolios, and ensured timely, ethical, and high-quality trial delivery. Throughout my career, I have remained committed to patient safety, regulatory excellence, and advancing medical research.
Revisions: #
2
Timeline (days):
14
Price: from USD $
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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