Panoptic Clinical Trial Solutions: Targeted Solutions for CROs - Freelance Contractor PMs and CRAs
We offer freelance (contractor) clinical research support for Contract Research Organisations (CROs).
Here’s how we can help you:
In addition to typical freelance services, Panoptic offers targeted specialist services to streamline specific stages of clinical trials.
Take the pressure off your in-house team, by supplementing your projects with freelance clinical trial specialists from Panoptic Clinical.
By leveraging Panoptic Clinical’s expertise and flexible services, CROs can deliver exceptional service to their clients for successful clinical trials and repeat business from clients.
Freelance Services for Contract research Organisations
Clinical Operations
Clinical Operations support can help improve efficiency during all stages of a clinical trial at a project, program or departmental level, such as:
- During Start-Up with review of the protocol to identify potential roadblocks or potential for scope creep. With developing project budgets, negotiating site contracts.
- As the project moves towards clinical conduct, operations support can be utilised to provide high level oversight of clinical monitoring and may include on-site oversight/assessment/co-monitoring visits with CRAs to ensure adherence to regulations, protocol, SOPs and GCP.
Clinical Project Management
A Panoptic freelance Clinical Project Manager (CPM) can easily step-in and manage an entire clinical trial, or to supplement your in-house Project Manager (PM) but taking on specific tasks such as:
Feasibility and Site Selection
Budget development
Site contract (Clinical Trial Research Agreement) and budget negotiation
Vendor management
Development of project plans (Risk Plan, Communication Plan, Monitoring Plan etc.) and study manuals (laboratory manual, pharmacy manual)
Clinical Monitoring / Clinical Research Associate (CRA)
Utilise Panoptic freelance CRA services for full project clinical monitoring, or to support your internal team with specific tasks such as:
Unblinded monitoring / pharmacy monitoring
Site selection Visits / Site Qualification Visits
Dose Witness Visits
On-site or remote monitoring
Trial Master File (TMF) review
Training and Mentoring
Training of site staff such as when face to face on-site visits are required for device training, Investigational Medicinal Product (IMP) dosing practice run
Mentoring of internal PMs or CRAs, including on-site co-monitoring visits
Specialist Services for Contract research Organisations
Specialist Kick-Start
Get your Australian clinical trial off to a flying start with the assistance of our freelance start-up specialists. We offer comprehensive support during the critical start-up phase, including:
Feasibility and Site Selection
Ethics and Regulatory Applications
Contract Negotiation
Specialist Boost
Encountering a bottleneck during your clinical trial? Panoptic’s Boost services provide the extra muscle you need to overcome challenges and stay on track. We offer specialised freelance talent to augment your existing team, particularly during busy periods such as interim analysis and database lock. Typical services including on-site clinical monitoring and remote monitoring.
Specialist Wrap-Up
As your clinical trial nears completion, Panoptic’s Wrap-Up services ensure a smooth and efficient completion. Providing expert support in:
Trial Master File (TMF) Review
Site Close Out Visits