Development of detailed, patient-centred trial protocols.

Feasibility assessments to identify risks and optimise resources.

Endpoints and outcomes planning tailored to your objectives.

Innovative trial methodology design for efficiency and accuracy

Regulatory submissions, including REC and MHRA applications.

Vendor and site selection, including contract negotiations.

Training for investigators and site staff on trial protocols and compliance.

TMF and eTMF creation and management.

End-to-end project management of timelines, budgets, and deliverables.

Ongoing risk management and mitigation strategies.

Stakeholder coordination, including sponsors, investigators, and vendors.

Regular monitoring of trial progress to ensure adherence to protocols.

Comprehensive Good Clinical Practice (GCP) Training for all staff, ensuring compliance and understanding of industry standards.

Trial-specific training tailored to investigators, coordinators, and site staff.

Customised Company Workshops: Interactive sessions designed to enhance organisational understanding of clinical trial processes, compliance, and best practices.

Mentorship for clinical trial professionals, including trial coordinators, assistants, and managers.

Open consultations for any questions related to clinical trial operations.

Applications / Interview tips and prep