Our operations team have broad and deep insights in the local ethics and regulatory framework. They also have strong relationships with investigators and their teams. We are scientists with a passion for operationalising clinical research and we have built a robust reputation of delivering faster, better and to a higher standard.
At ClinMed Pharma we believe that study feasibility is an ongoing activity. We listen carefully to our investigators and their peers to collect ongoing insights and share these with study sponsors on an ongoing basis. This allows for well-informed decision making throughout the programme.
We are very proud of our broad diversity within our network. The solid reputation of our organisation locally enables our start-up team to accelerate the set-up of studies at an impressive pace.
Our biostatistics and data management team are integrated within our clinical operations team. Together, we review data and ensure that you get the best value on every point of data collected.
We take a clinical development plan at any stage of maturity and provide valuable insights so that important decisions can be made quickly. Our clinical operations team build trust in every interaction so that we can exceed expectations.
Research question familiarisation
Broad intelligence gathering: experts, analysts and databases
Comprehensive analysis and forecasting of: Scientific and Clinical Feasibility Patient recruitment Timelines Budget Probability of success
Our dedicated study start-up specialists have developed leading processes and systems to accelerate the start-up of studies. Our strong relationships with investigators and their teams globally allows us to progress studies with speed and agility.
Contrary to popular belief, patient recruitment can be projected accurately. At ClinMed Pharma we use deep insights in the therapeutic area, local epidemiology data, clarity on the target patient population, the treatment landscape, precedence and local site intelligence to accurately project patient recruitment.
Our team have successfully accelerated patient recruitment in extremely niche patient populations, enabling the timely generation of clinical evidence. We think outside the box to make this happen and work with a broad range of specialists:
All solutions below conform to local laws and regulations.
Study Branding and Website Development
Animation of Patient Information
Study Advertisement and Social Media Outreach
Engagement with patient advocacy groups
Affiliation with patient support charities
Sponsorship of Patient Targeted Education Material
Provide resourcing solutions to investigators where required
Establish Centres of Excellence & Hub-and-Spoke Models
Create a robust investigator community (global/local)
Interface with local multi-disciplinary team meetings
Leverage databases for patient identification
Supporting sites in harnessing the power of eHR
We can’t eliminate risk but we can identify, characterise and proactively manage it. ClinMed Pharma have successfully conducted numerous studies with a truly risk-based monitoring strategy. We work closely with you to categorise all aspects of the study programme to three levels of risk. From study design to sections of the protocol, site selection through to datapoint level – we have it covered. We understand that risk is dynamic and our systems and processes allows for complete visibility of the dynamic nature of risk and also for re-categorisation should it be required.
Our project management team at ClinMed Pharma have “T-shaped” skills in clinical research. They have the depth and breadth of expertise in cross-functional partnerships. Their ability to problem-solve combined with adept soft-skills ensure our customers consistently receive the highest level of service. Your study will receive.
We work cross-functionally with our events management and creative partners to provide our customers with the best training experience. From investigators meeting to GCP training we make the ordinary engaging and memorable. Our training team expertly execute a broad remit from SOP training, to GDPR and study motivational meetings with external experts to Oxford-style debates, we simply do it better.