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    Ascent CRS is a full-service CRO that provides an entire range of clinical research services from Phase I and Proof of Concept to Phase III-IV and Bioequivalence studies.

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We are Ascent. We know clinical trials.

Ascent CRS offers full-service project management for every stage of your clinical trial. With our highly professional team you can be confident that you trial whether it’s an exploratory design study or late phase trial is in right hands to be conducted timely, correctly and on an agreed budget.

Our team has experienced project leaders on board, who have multiple years of industry experience, and vast clinical and therapeutic practice, especially in complex and critically ill patient populations.

We aim to excel at all stages of study operations:

Feasibility and risk analysis
• Investigation sites recruitment and qualification
Development of project-specific procedures and guidelines
• Pre-study phase and site training
• Investigator and hospital contracts
• Study management and study logistics
Finance and Contract Management
• CRA training and coaching
Quality control management
Safety surveillance and pharmacovigilance

Our project managers:

✓ Ensure GCP adherence
✓ Provide you and study vendors a single point of contact
✓ Put risk and contingency plans in place which anticipates and prevents problems
✓ Manage budgets to minimize change orders
Keep you as informed as you need to be through frequent communications
Escalate important issues quickly and offer solutions
Take ownership of your project and all its deliverables

Our project leaders are the study managers and partner and key point of contact with the sponsor. They create the best suited team for each clinical program and remain responsible throughout the whole trial and supervise the study schedule up to the production of the final report.

As the primary point person, project managers is responsible for overseeing all interactions, managing study sites, coordinating investigator payments, monitoring study metrics, training, assuring adherence to timelines, and coordinating interactions among operations teams.

Our Project Management Approach is based on an ongoing anticipation and management of issues, and offering proactive solutions. Through meticulous planning and co-ordination, our project management model aims to deliver projects with clear focus on providing quality backed by on time and on-cost deliverables.

Our experienced and highly-qualified project managers ensure that your study timelines are met. For the duration of your project, we are focused on consistent quality control to achieve the highest quality data possible.

All our project managers go through extensive therapeutic training, including standard operating procedures (SOPs), Good Clinical Practice guildelines (ICH-GCP) and study specific training on an ongoing basis and at the beginning of each study. Internal audits are also done in conjunction with the project manager to ensure that training is completed.

We believe, that strong project management and close contact with the sponsor are important keys for successfully conducting clinical trials.