Founded in 2006, KPS Life is a standalone functional service provider (FSP) that offers global functional clinical trial outsourcing services to sponsors. Its services include clinical monitoring, clinical oversight, clinical trial management, data management, eTMF and document management, vendor qualification, and medical writing. KPS Life’s operations span six continents and more than 33 countries.

KPS Life is uniquely devoted to providing customized, outsourced clinical solutions to pharmaceutical and biotech customers of all sizes across all stages of clinical trials. KPS Life is committed to working together with its customers through a hands-on operating model rooted in a partnership approach. The Company has carved out a leadership position by prioritizing the needs of its customers, flexibility, accountability, cost savings, and transparency. KPS Life serves as an active resource to potential customers in optimal FSP design as they transition from the full-service model or other FSP providers to KPS Life. Visit our website: https://kpslife.com/


KPS Life offers a smaller, and smarter, alternative. We bring “A-Team” resources that are 100% dedicated to our Sponsors — and create a collaborative, supportive process where you maintain complete control of operations.

The hard truth is: Clinical Oversight is essential — and required. Ensuring that your trial is delivered with the highest of quality, on time, and on budget is essential with the escalating costs to conduct clinical trials and to avoid unnecessary and often required, change orders.

Our industry-leading clinical analytics experts build tools and solutions that efficiently facilitate data management and biometrics activities. We carry this out by automating and applying advancing services and technology to maximize trial efficiency, ease interpretation, and prepare your clinical trial data to quickly deliver actionable insights.

KPS is NOT a clinical staffing firm. But as a well-integrated FSP, we maintain personal relationships with some of the most highly experienced and sought-after clinical professionals in the industry.



10 Valley Stream Parkway

Malvern, PA 19355


Contact: Sean Quinn


  • Read about the continuous evaluation and varying opinion regarding the strategic resourcing models employed within the biopharmaceutical sector today.

  • Ensuring that your trial is delivered with the highest quality, and also on time and on budget, is essential with the escalating costs to conduct clinical trials and to avoid unnecessary and often required change orders. This infographic reviews 5 key takeaways for controlling clinical trial costs while building a focus on quality from the beginning.

  • Sponsors and CROs employ CRAs to monitor clinical study sites. Because most site monitoring is done in the field, it is challenging for study managers to know and understand if CRAs/monitors are conducting their duties effectively and efficiently. Many study sponsors therefore employ co-monitoring/oversight visits to directly evaluate CRA performance and facilitate training. The following process can help to achieve successful co-monitoring/oversight visits.