Clinical Operations

Delivering High Quality Clinical Operation Services Through Our People, Powered By Technology

Clinical operations refer to the management and coordination of activities within a clinical trial or healthcare industry to ensure the smooth running of operations. 

SafeVig’s clinical trial managers provide leadership and operational expertise through collaborative planning, implementation, and execution. From start-up to close-out, our highly skilled clinical operations teams ensure proper planning, conduct, patient safety, and data quality while fostering good communication between study sites and sponsors. Our Clinical Operations team is experienced in managing clinical trials of varied sizes and complexity in different therapeutic areas.

Clinical research associates work closely with your team on protocol and indication training, building strong site relationships, and ensuring site compliance. SafeVig’s vast network of clinical trial experts provides global consistency, support, and a high-quality standard, meeting ICH-GCP guidelines wherever in the world.

We offer comprehensive clinical trial management solutions, whether you require support or seek to design a tailored, end-to-end clinical program. Our seasoned and knowledgeable team is poised to collaborate with you in crafting a program perfectly suited to your unique requirements.

Our operational expertise can be utilized for Phase I to IV clinical trials, including proof of concept study. We specialize in managing the following Clinical Operation activities:

Project Management

Study Feasibilities

Site Evaluation and Selection.

Contract Execution

Patient Recruitment And Retention

Site Monitoring And Management

Trial Master File Management

CRA Management And Quality Control

Third Party Vendor Selection And Management

Audit Preparation

IRB/EC Submissions

Full Service Monitor Visits

Rapid Query Resolution

Drug Accountability

Site Training And Support

Timely Completion of Visit Reports

In Country Expertise For Feasibility Or Regulatory Submissions

Source Document Verification As Per Monitor Plans

Comprehensive Monitor Plans

Quality Review Of Monitor Reports

Site Management Support And Documentation

Periodic Remote EDC Review

A Thorough Review Of Site Records

To Find Out More, Contact Us Today!