Streamline Your Study Start Up with Precision

Failing to plan means planning to fail. Precision teams tailor each study startup approach to the unique needs of sponsor partners, strategizing from day one to align all the pieces needed to activate sites on time and enroll patients quickly. Working in a fast-paced environment calls for thinking several steps ahead. We set ambitious targets with built-in buffers and meticulously calculate the steps and timing needed to achieve milestones.

We understand the impact of cross-functional collaboration on timelines. That’s why feasibility and site identification, regulatory, contracts, and clinical work together seamlessly under the same roof. Whether it’s leveraging our expertise in countries primed for speedy startup or navigating complex regulatory landscapes, we develop the optimal activation strategy for sponsor programs.

Collaboration and client service are core principles of Precision and its people. We proactively identify and mitigate risks to prevent delays down the line. Every contract, regulatory document, and submission benefits from this approach, avoiding costly rework and missed milestones.

In the world of startup, accountability is crucial. At Precision, our team members understand the importance of bringing together many different pieces and taking ownership. It’s easy for people to say, "This is not my job," but at Precision, every team member takes responsibility to ensure nothing is overlooked.

We’re one team, united in our relentless pursuit of success. Together, we can accelerate patients’ access to potentially life-changing therapies. Our culture of accountability, mutual respect, and collaboration ensures that we partner with you to bring your drug to market quickly and with high quality.

You should work with Precision because of our people and their culture of accountability and collaboration. We have the right expertise and experience to partner with you, ensuring that your clinical trials are set up for success from the start.