Keep Your Trials Moving Forward

Keeping your study on track is essential to reduce costs, stay ahead of competitors, and meet development timelines. Delays risk falling behind in the market and can lead to resource inefficiencies. Ongoing progress ensures timely data collection, smoother regulatory approval, and better participant retention. Maintaining momentum strengthens investor confidence and accelerates bringing your drug to market. Let’s work together to overcome challenges and keep your study moving forward, ensuring its successful completion.

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A clinical research consultant offers expertise in trial design, management, and optimization, ensuring regulatory compliance and improving efficiency. They help with complex protocols, data analysis, patient safety, budgeting, recruitment, and overcoming challenges, ultimately enhancing research quality, reducing risks, and increasing the likelihood of a successful trial.

FlyOver Clinical is NOT a CRO.  I am an independent trial consultant providing a la carte services to the benefit of my clients, patients, and medicine in general.  Here are a few reasons you might want to work with me:

  • Temporary staff coverage due to illness, parental leave, or other unexpected absences 
  • Additional staffing needed but lacking the resources to hire another employee
  • Experienced person needed to guide and train junior staff

Whatever you need, whenever you need it!

Unlock the flexibility of tailored clinical trial support with a la carte services. Whether you’re conducting early-phase studies, expanding into late-stage trials, or managing complex global research, Flyover Clinical can provide customizable solutions that meet your needs. From patient recruitment, to site monitoring, to data management, I provide clinical trial services designed to optimize efficiency and accelerate your timeline.

Flexibility and responsiveness are my highest priorities. From quick-turnaround tasks to long-term project management, I am committed to meeting your deadlines and exceeding expectations. Together, we can navigate complexities, optimize efficiency, and drive your clinical trial to success.

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Medical Writing

My medical writing skills can help with:

  • Protocol Development
  • IRB Submissions
  • Case Report Form (CRF) Development and Design
  • Informed Consent Forms (ICFs) Drafting

Data Management

  • Database (EDC) Validation
  • Data Entry
  • Data Cleaning
  • Query Generation and Closing
  • Database (EDC) Design

Clinical Trial Monitoring

  • Domestic or International
  • On-Site or Remote
  • Site Qualification Visits
  • Site Initiation Visits
  • Interim Monitoring Visits
  • Study Closeout Visits

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