We provide clinical operations services across the full lifecycle
from start-up, patient recruitment, monitoring, CRO oversight through close-out activities
and inspection preparation support for Phase I - Phase III trials
Our Mission
With close to 20 years of global clinical development experience, we partner with pharmaceutical and biotechnological organizations to accelerate clinical development timelines through clinical operations excellence with adherence to ICH-GCP guidelines and regulatory requirements.
Our expertise spans multiple therapeutic areas and treatment modalities. We deliver customized end-to-end support that enhance operational efficiency, advance your pipeline, and help achieve your corporate objectives.
Our mission is simple — helping clients bring innovative therapies to patients sooner.
Our Focus
We provide strategic and hands-on and results-driven support to pharmaceutical and biotechnological organizations worldwide.
With extensive global experience, we will help you to translate scientific and clinical strategy into operational excellence ensuring your clinical trials are executed with rigor, efficiency and a clear focus on patient impact.
Services & Expertise
Strategic and hands-on clinical operations services across the full lifecycle - from start-up, patient recruitment, monitoring, CRO oversight through close-out activities and inspection prep support.
Start Up Activities
We will help you to manage all critical start-up activities to ensure your trial launches efficiently and on time — from site identification, CRO selection and feasibility assessments to regulatory submission support, contract execution, and site initiation. Our structured approach accelerates first-patient-in while maintaining quality and compliance at every step.
CRO Oversight
We partner with sponsors to ensure CRO activities stay aligned with study goals, timelines, and quality standards. Through proactive oversight, clear communication, and risk management, we help keep outsourced studies on track and accountable.
Site & Recruitment Mgmt.
We understand the importance of establishing and maintaining positive relationships. We will drive the development and implementation of strategies to facilitate timely enrollment and optimal use of all resources and supplies.
Close-Out Activities
We partner with sponsors and drive seamless study close-out activities, ensuring all data, documentation, and regulatory requirements are completed accurately and on time. Our proactive approach minimizes delays, resolves outstanding issues, and helps deliver a clean, audit/ inspection ready study.
Monitoring Oversight
We partner with sponsors to oversee monitoring and CRA activities, ensuring consistent site engagement, protocol compliance, and high-quality data. By providing guidance, support, and transparent communication, we ensure CRAs address issues proactively and keep your study running smoothly and in compliance with the protocol and the monitoring plan.
Inspection Preparation
We help sponsors prepare for and navigate FDA inspections with confidence. We ensure your team and sites are inspection-ready while maintaining compliance and minimizing risk.
Why Work With Us
We partner with you to achieve operational excellence & accelerate the delivery of innovative therapies to patients
Strategic Experience with Global Perspective
We bring close to 20 years of experience in global clinical operations, having led complex portfolios across the Americas, Europe, APAC, and Africa. My background combines hands-on operational leadership with a deep understanding of clinical development strategy, governance, and regulatory expectations.
Tailored & Pragmatic Solutions
Each client and program is unique. We work closely with organizations to design operational strategies that are realistic, compliant, and aligned with corporate objectives — ensuring every project delivers measurable impact without unnecessary complexity.
Collaborative & Transparent Approach
Clear communication and trust are at the core of how we work. We partner closely with teams to anticipate challenges early, foster accountability, and maintain open dialogue from study planning through delivery.
Contact Us
Whether you need strategic guidance, operational leadership, or full-service clinical operations support, we are here to help!
Ready to accelerate your clinical programs? Get in touch today to discuss how we can help advance your development programs efficiently, compliantly, and strategically.
A bit more about about the founder...
Awo Kankam
With close to 20 years of global clinical operations experience, I help Biopharma and Biotech organizations bring therapies to patients faster. I partner with teams to streamline study delivery, optimize operational performance, and align clinical strategies with business priorities.
I’ve built and scaled high-performing teams, led complex global trial portfolios across rare diseases, oncology, vaccines, dermatology, and infectious diseases, and ensured compliance with ICH-GCP and local regulations across the Americas, Europe, APAC, and Africa.
Fluent in English and German, I thrive on fostering cross-functional collaboration and delivering measurable results that advance both pipelines and corporate goals.
