Clinical Research Operations
At Proven Sciences in Saudi Arabia, we understand the importance of effective communication and tailored solutions in clinical project management. We prioritize close collaboration with our clients to identify and address their specific needs throughout each clinical study project, even as priorities may shift.
Our project managers and leads are seasoned professionals with an average of 15+ years of experience. They recognize the significance of stakeholder relationships and are dedicated to delivering high-quality results that make a difference. Additionally, they provide valuable guidance and ensure the achievement of preplanned milestones.
Key Features of Our Services Include:
- Performance Quality
- Ensuring that each step of the study is completed with exceptional quality to meet rigorous standards.
- Adherence to Timelines
- Ensuring that all project timelines are meticulously met, keeping the project on track within defined parameters and in coordination with our sponsors.
- Budget Management
- Assisting our clients in managing project budgets effectively, ensuring that studies are completed within budgetary constraints and minimizing unnecessary additional costs.
At Proven Sciences, we are committed to delivering excellence in clinical project management, providing our clients with the confidence and support they need to achieve their goals.
Our Team
Proven Sciences in Saudi Arabia offers comprehensive clinical monitoring services supported by our experienced Clinical Research Associates (CRAs), Clinical Research Leads, and Clinical Operations Managers. Our services cover all stages of clinical trials, from feasibility assessment to site closeout, and are tailored to meet the specific needs of each project in the MEA Region.
Key Features of Our Clinical Monitoring Services:
- Tailored Clinical Support
- Our clinical services are customized to align with your specific needs, complementing product development plans and corporate quality management policies.
- Compliance and Quality Assurance
- All monitoring activities are conducted in strict adherence to the study protocol, clinical monitoring plan, standard operating procedures, ICH GCP guidelines, and relevant local and regional regulations.
- Comprehensive Monitoring Activities
- Our team covers all aspects of study monitoring, including feasibility assessments, site qualification and initiation visits, interim monitoring visits, and closeout visits.
- Logistic Support and Training
- We provide logistic support for site supplies and offer training to site teams as needed, ensuring smooth conduct of clinical activities and adherence to study protocols.