Helping the Community and the World One Patient at a Time
Geodyssey Research, LLC is multi-specialty Clinical Research Coordinating Service that partners with a select core of both Principal Investigators and Pharmaceutical Companies.
Our Services to the Investigator include:
Marketing, Advertising and Business Development
Coordinating clinical trials according to ICH/GCP guidelines
Patient Recruitment and Retention
All Research activities take place at your location
Lower labor costs due to study specific contracts
To the Sponsor and CRO we offer:
Over sixteen years experience Coordinating numerous trials
Knowledge that all potential sites have been evaluated by our staff
Expertise with all Regulatory Documents
Experience with Project Management from the Sponsor’s point of view
Availability for all Monitoring visits and/or audits
Disease specific database searches within HIPAA guidelines
Our promise to all of our clients is to provide clean data, on a timely basis, emphasizing a good-faith effort to meet or exceed promised enrollment goals.
Benefits to Physicians
Thought leader in medical science and treatments
Generates additional income for existing practice
Helping those most in need
Reduces costs and time associated with conducting clinical trials on your own
What will this cost you?
Your overhead is already established. This will only generate income to your already established practice.
Geodyssey Research, LLC Responsibilities
Schedule and Conduct all Patient Visits
Properly market the Investigators to Sponsors and Contract Research Organizations
Attend Investigator Meetings with at least one representative
Negotiate budgets and language of the contracts
Prepare and negotiate all advertisements
Complete feasibility questionnaires
Review and analyze protocol synopsis’ to determine the feasibility of the trial.
Prepare and maintain all regulatory documents required for the review committees and the FDA in accordance with ICH/GCP guidelines
Track patient visits and procedures
Pay outsourced procedures and patient visit stipends
Prepare for monitoring visits as dictated by the Sponsor (i.e. ensuring administrative documents, patient charts, and case report forms are in good order)
Completing Case Report Forms and/or Electronic Data capture
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