Seeking an optimal CRO partner for your biotech success? 

We understand the challenges biotechs face when engaging with Contract Research Organizations (CROs). Often, there are obstacles in securing the dedicated resources and attention you deserve. 

Say goodbye to rigid processes, suboptimal quality, delays, being unheard and high costs. Let's navigate the biotech maze together, finding specialized, flexible, and cost-effective solutions.

We prioritize your needs, ensuring your voice is heard and goals are met. Our streamlined processes and tailored solutions deliver resources efficiently. 

With our expertise, expect tangible results driving your biotech forward. Experience faster timelines, optimized budgets, enhanced communication, and access to a valuable resource network

Years in Clinical Research and Business Consulting

Successful Projects

Countries Served

Elevate Your Voice, Amplify Your Impact

Integrated Teams Functional Outsourcing Flexible Resourcing and Insourcing

At SuperNOVA, we're more than just another consultancy or CRO in clinical research – we're advocates who truly make your vision as our drive.

We recognize that a one-size-fits-all approach doesn't cut it. At SuperNOVA, we offer dynamic and adaptable insourcing, outsourcing or FSP models tailored to your unique requirements. With over 5,000 experts in our network, we can scale up or down immediately. Our agile functional teams encompass a wide range of expertise, including clinical operations, project leadership/governance, regulatory affairs, medical writing, quality/compliance, and safety.

Seamless integration is at the core of our approach. We believe that collaboration should be effortless, impactful, high-quality and efficient. With our agile teams and streamlined processes, we seamlessly integrate with your operations, providing a frictionless experience. Our experts become an extension of your team, working hand in hand to deliver exceptional results. 

 

You have the freedom to start with a single expert, or you can access our comprehensive functional team models for a holistic solution whether you would like to outsource or run trials in-house.

SuperNOVA Clinical Research is more than just a service provider – we are your transformative partner. We go beyond the conventional consultant-client or CRO-client relationship, striving to understand your unique vision and goals. Our commitment to building strong and enduring partnerships sets us apart. We proactively support you every step of the way, offering strategic guidance, innovative solutions, and dedicated resources.

From driving clinical development to fostering meaningful patient engagement, we consistently exceed expectations. Our commitment goes beyond the norm as we build strong and enduring relationships, delivering proactive support that empowers you every step of the way.

Integrated Teams Functional Outsourcing Flexible Resourcing and Insourcing

services

How can we Help?

Clinical Research

Clinical Research Oversight

Streamlined clinical trial execution from A to Z

Imaging Solutions

Centralized Radiology Imaging Solutions

Seamless, Accurate and Consistent Image analysis, reporting, management, and advanced technologies

Development

Training and Coaching

Enhancing leadership, performance, and productivity

What we do

Our Solutions & Capabilities

Centralized Clinical Trial Radiology Imaging

Optimize radiology imaging processes in clinical trials for improved efficiency and accuracy.

Governance and Strategic Oversight

Provide strategic oversight and establish governance frameworks to ensure regulatory compliance and goal alignment.

Portfolio | Program or Project Leadership

Drive successful outcomes, offer expert portfolio, program, or project management leadership.

CRO and Vendor Selection

Identify and partner with suitable CROs and vendors through comprehensive selection processes.

Vendor Management and Oversight

Efficiently manage vendor relationships to ensure adherence to timelines, quality standards, and contractual obligations.

Clinical Operations (Monitoring & Clinical Trial Management)

Manage clinical trial operations, including monitoring, data collection, and site coordination for compliance and data integrity.

Clinical Quality Assurance

Ensure compliance, data integrity, and patient safety in clinical trials.

Data Management & Medical Writing

Ensuring accurate data analysis and effective scientific communication.

Regulatory and Safety

Provide expert guidance and ensure compliance throughout product development.

Decentralized Clinical Trials

Facilitate remote participation and data collection in clinical trials through innovative strategies and technologies.

Content Management

Organize and distribute information effectively through robust content management systems.

Patient and Site Engagement

Engage patients and sites actively in clinical trials to enhance participation, compliance, and retention.

Organizational Excellence

Drive process optimization, performance metrics, transitions acceptance and continuous improvement initiatives for organizational excellence using six sigma, lean and change management.

Training and Coaching

Enhance research teams' skills, knowledge, and performance through comprehensive training programs and coaching services.