Research Management Services
The Clinvest Research Management staff has many years of experience conducting and providing oversight for projects with the investigators from the Clinvest research network.  Our goal is to promptly recruit qualified investigative sites, manage study startup activities, and oversee with proficiency the responsibilities assigned by the sponsor.

Investigative Site Recruitment
Information in the database allows site recruitment based on sponsor-specified criteria including but not limited to Demographics, Certification, Practice size or specialty, Areas of interest, and Research experience.  A close working relationship with sites enhances communication and increases compliance resulting in successfully run trials.

Pharmaceutical Industry-Sponsored and Investigator-Initiated
Research Studies            

Complete Research Services

Protocol development/review
Informed consent development/review
Develop Study Timeline
Design/Produce CRFs
Design/Produce Data Collection tools
Regulatory Management
IRB Submission
Clinicaltrials.com registration
Project Management
Site Training
Develop Monitoring Plan
Oversee Study Monitoring
Site Clinical Study Agreement Management
Payment to Patients and Sites
Develop Data Management Plan
Design/Develop Test Collector and Queries
Data Entry
Data Review/Cleaning
Data Transfer to Sponsor
Develop Statistical Analysis Plan
Conduct Statistical Analysis
Develop/Submit Manuscript to Scientific Journal
Presentation at Scientific Meetings